Corn plants with improved disease resistance

Abstract

Corn plants exhibiting broad-spectrum resistance to Exserohilum turcicum are provided, along with methods for creating, identifying, or selecting plants or genetic resources with an Exserohilum turcicum-resistant phenotype. Such plants include sweet corn plants containing an introgressed genomic region that confers disease resistance, as well as agronomically elite dent corn plants. Compositions containing novel polymorphic markers and methods for creating, breeding, identifying, and selecting plants or genetic resources with disease-resistant phenotypes are also provided.

Description

[Technical field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This application claims the benefit of priority to U.S. Provisional Patent Application No. 62 / 783,899, filed December 21, 2018, the disclosure of which is incorporated herein by reference in its entirety.

[0002] Incorporating sequence tables The sequence listing, including a 4 kilobyte (measured in MS-Windows®) file named “SEMB040WO_ST25.txt” created on December 17, 2019, containing five sequences, is incorporated herein by reference in its entirety.

[0003] FIELD OF THEINVENTION The present invention relates to the field of plant breeding, and more specifically, to methods and compositions for producing corn plants exhibiting improved disease resistance. [Background technology]

[0004] Disease resistance is an important trait in agriculture, especially for the production of food crops. In maize plants, disease resistance alleles have been identified, but efforts to combine several disease resistance traits in a single plant line have been hampered by closely linked genetic or even allelic loci that confer resistance to different pathogens. The introduction of disease resistance is further complicated by the high density of repetitive sequences in the regions of the plant genome that control disease resistance, which can greatly reduce the possibility of developing useful genetic markers. Identification of additional genes that confer resistance to multiple pathogen races is desirable. Summary of the Invention

[0005] The present invention provides an agronomically elite corn plant comprising an introgression from Zea mays var. indentata on chromosome 8, the introgression comprising a single gene that confers broad-spectrum resistance to Exserohilum turcicum compared to a plant lacking the introgression, the resistance being additive. In certain embodiments, the introgression comprises a chromosome segment from Zea mays var. indentata at marker M1 (SEQ ID NO: 1) of the plant. In further embodiments, the introgression is about 12 cM or less in size. In yet other embodiments, the plant is homozygous for the introgression. In additional embodiments, a sample of seed comprising the introgression was deposited under ATCC Accession No. PTA-125393.

[0006] In certain embodiments, broad-spectrum resistance includes resistance to multiple Exserohilum turcicum races. For example, broad-spectrum resistance includes resistance to Exserohilum turcicum races 1, 2, M, and N.

[0007] The present invention provides a plant part of a corn plant comprising an introgression from Zea mays var. indentata on chromosome 8, the introgression comprising a single gene that confers broad-spectrum resistance to Exserohilum turcicum compared to a plant lacking the introgression, the resistance being additive. In certain embodiments, the plant part is a cell, seed, root, stem, leaf, panicle, flower, or pollen.

[0008] Additionally, the present invention provides an introgression fragment comprising a chromosomal segment from Zea mays var. indentata at marker locus M1 (SEQ ID NO:1). In certain embodiments, the fragment confers broad-spectrum resistance to Exserohilum turcicum. In other embodiments, a seed sample comprising the introgression was deposited under ATCC Accession No. PTA-125393.

[0009] The present invention also provides a method for producing an agronomically elite corn variety plant with improved resistance to Exserohilum turcicum, comprising introgressing into the plant a chromosome segment from Zea mays var. indentata on chromosome 8 that confers broad-spectrum resistance to Exserohilum turcicum compared to a plant lacking the introgression, wherein the resistance is additive. In some embodiments, the broad-spectrum resistance comprises resistance to multiple Exserohilum turcicum races. In further embodiments, the broad-spectrum resistance comprises resistance to Exserohilum turcicum races 1, 2, M, and N. In yet another embodiment, a sample of seed comprising the chromosome segment was deposited under ATCC Accession No. PTA-125393. In some embodiments, the introgression comprises backcrossing. In other embodiments, the introgression comprises marker-assisted selection. In certain embodiments, the introgression comprises assaying for the broad-spectrum resistance to Exserohilum turcicum. In some embodiments, introgression comprises crossing a plant containing the chromosome segment with itself or with a second corn plant of a different genotype to produce one or more progeny plants and selecting a progeny plant containing the chromosome segment. In certain embodiments, selecting a progeny plant comprises detecting a nucleic acid comprising marker locus M1 (SEQ ID NO:1). In further embodiments, the progeny plant is an F2 to F6 progeny plant. In selected embodiments, producing the progeny plant comprises backcrossing. The present invention further provides corn plants obtainable by the methods provided herein.

[0010] Additionally, the present invention provides a method for selecting an agronomically elite corn with improved resistance to Exserohilum turcicum, comprising crossing a corn plant comprising an introgression from Zea mays var. indentata on chromosome 8, the introgression comprising a single gene conferring broad-spectrum resistance to Exserohilum turcicum compared to a plant lacking the introgression, the resistance being additive, with itself or with a second corn plant of a different genotype to produce one or more progeny plants, and selecting a progeny plant comprising the introgression. In some embodiments, selecting the progeny plant comprises detecting a marker locus genetically linked to the introgression. In certain embodiments, selecting the progeny plant comprises detecting a nucleic acid comprising the marker locus M1 (SEQ ID NO:1). In other embodiments, the resistance comprises resistance to multiple races of Exserohilum turcicum. In further embodiments, the resistance comprises resistance to Exserohilum turcicum races 1, 2, M, and N. In some embodiments, the progeny plants are F2 to F6 progeny plants. In other embodiments, generating the progeny plants comprises backcrossing.

[0011] Additionally, the present invention provides an agronomically elite corn plant comprising an introgression from Zea mays var. indentata on chromosome 8, the introgression comprising a single gene that confers broad-spectrum resistance to Exserohilum turcicum compared to a plant lacking the introgression, the plant further comprising a recombinant chromosome segment comprising a first allele comprising an Ht2 locus and a second allele comprising an HtN locus, the first allele and the second allele being arranged in cis-linkage on chromosome 8, the recombinant chromosome segment conferring resistance to Exserohilum turcicum. In some embodiments, the recombinant chromosome segment is adjacent to marker loci Q-NZMAY009401770 (SEQ ID NO:2) and Q-NZMAY009430172 (SEQ ID NO:5) on chromosome 8. In other embodiments, the recombinant chromosome segment is adjacent to marker loci Q-ZMHt2 (SEQ ID NO: 3) and Q-NZMAY009238970 (SEQ ID NO: 4) on chromosome 8.

[0012] Additionally, the present invention provides an agronomically elite dent corn plant comprising an introgression from Zea mays var. indentata on chromosome 8, the introgression comprising a single gene that confers broad-spectrum resistance to Exserohilum turcicum compared to a plant lacking the introgression. In some embodiments, the introgression comprises a chromosome segment from Zea mays var. indentata at marker M1 (SEQ ID NO: 1) of the plant. In other embodiments, the broad-spectrum resistance comprises resistance to multiple races of Exserohilum turcicum. In some embodiments, the plant is homozygous for the introgression. In other embodiments, a seed sample comprising the introgression has been deposited under ATCC Accession No. PTA-125393.

[0013] Additionally, the present invention provides a method for producing an elite corn variety plant with improved resistance to Exserohilum turcicum, comprising introgressing into the plant a chromosome segment from Zea mays var. indentata on chromosome 8 that confers broad-spectrum resistance to Exserohilum turcicum compared to a plant lacking the introgression, wherein the resistance is additive. In some embodiments, the introgression comprises crossing a plant containing the chromosome segment with itself or with a second corn plant of a different genotype to produce one or more progeny plants; and selecting a progeny plant that contains the chromosome segment. In some embodiments, the selection of a progeny plant comprises detecting a nucleic acid that includes the marker locus M1 (SEQ ID NO:1). In other embodiments, the elite corn variety is a dent, flint, or sweet corn variety. In some embodiments, the progeny plant is an F2 to F6 progeny plant. The present invention further provides a corn plant obtainable by the methods provided herein. [Brief description of the drawings]

[0014] [Figure 1] Figure 1 shows the compatibility profile between Exserohilum turcicum races and Ht genes. "S" indicates that the gene and race are compatible, and therefore plants carrying this gene are susceptible to that race, and "R" indicates that the gene and race are incompatible, and therefore plants carrying this gene are resistant to that race. [Diagram 2] 1 shows a graph displaying the distribution of Exserohilum turcicum races in major sweet corn market regions. [Diagram 3]Shown are the average disease indices (on a scale of 1 to 9) for two genetic backgrounds ("Hybrid 7" and "Hybrid 8") with differently positioned HtX genes tested at two locations in 2018. At the Wisconsin location, hybrids were inoculated with specific Exserohilum turcicum races. At the Florida location, the performance of hybrids against natural infection was tested. [Figure 4] The average disease index (on a scale of 1–9) is shown for six genetic backgrounds with differently positioned HtX genes ("Hybrid A," "Hybrid B," "Hybrid D," "Hybrid E," "Hybrid G," and "Hybrid H") tested in Florida in 2019. The performance of the hybrids against natural infection was tested. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0015] Northern leaf blight (NLB) is caused by the ascomycete fungus Exserohilum turcicum, also known as Setosphaeria turcica, and results in significant yield and quality losses in maize (Zea mays L.) crops. Exserohilum turcicum overwinters as dormant mycelium in host plant remains in the soil or as chlamydospores and infects new maize plants by airborne conidia. Depending on the host, pathogen, and environmental conditions, the first symptoms usually appear 14 days after infection and develop into oval, gray-green lesions 2-30 cm long that turn light brown along the leaf margins. In bad years or when host resistance is ineffective, the infection can spread throughout the leaf and lead to total leaf dieback. Infection occurs under favorable conditions of high humidity and moderate temperatures. This, combined with the fact that fungal lesions grow faster at night, makes the infection a particularly devastating disease of corn in tropical and subtropical regions. However, NLB is also present in corn in temperate regions. The impact of NLB can be reduced by fungicides, biological control, and improved management practices. The effectiveness of these methods can be increased if the plant is resistant to Exserohilum turcicum.

[0016] Resistance to NLB caused by Exserohilum turcicum comes in two forms: quantitative resistance, consisting of multiple loci that each contribute a small amount to the plant's resistance level, or qualitative resistance, consisting of a single race-specific gene that provides a high level of resistance. Qualitative resistance is often absolute, but to date, qualitative resistance to NLB in maize is not absolute and typically provides resistance that delays the onset of Exserohilum turcicum infection past the plant growth stage where infection has the most impact on yield and quality. Under environmental conditions favorable for Exserohilum turcicum growth, disease pressure can become severe enough to overcome qualitative resistance. Qualitative resistance is based on interactions between the plant's Ht genes and the fungal avirulence (avr) genes (Figure 1). If these interactions are incompatible, Exserohilum turcicum cannot infect the plant. To date, nine different Ht genes from different sources have been identified: Ht1 on chromosome 2, Ht2, HtNB, and Htn1 on chromosome 8, Ht3 on chromosome 7, ht4 on chromosome 1, HtM of unknown location, HtP on chromosome 2, and rt on chromosome 3. The nomenclature of these genes is directly related to the nomenclature of the races of Exserohilum turcicum. Each Exserohilum turcicum race is designated according to the Ht genes with which it is compatible, i.e., the race can infect plants that have the associated genes. For example, Exserohilum turcicum race 12 can infect plants that have the Ht1 and / or Ht2 genes. The genes HtNB and Htn1, both known herein as HtN and collectively referred to as HtN, are from different sources, but both are compatible with Exserohilum turcicum races that contain the avr gene and have the same resistance profile. Qualitative resistance is not necessarily durable, as the emergence of a compatible Exserohilum turcicum race can render the Ht gene ineffective.Furthermore, Exserohilum turcicum populations generally consist of a mixture of different races, with the race composition varying according to geographic region (Figure 2).

[0017] Therefore, breeders have generally attempted to combine different Ht genes to create resistant cultivars. However, this is not always easy or possible because Ht genes come from different sources and / or species, and the sources have diverse genetic backgrounds. In addition, it is difficult to combine genes in cis configuration when they are located in similar regions on the genome (such as Ht2 and HtN). It is even more difficult to introduce quantitative resistance into breeding populations, because small resistance effects of individual loci are difficult to detect, and breeders must ensure that all resistance genes are introgressed to obtain the resistance level of the donor plant. The ability to identify and use a single gene that confers resistance to all prevalent Exserohilum turcicum races would greatly simplify breeding and provide great benefits.

[0018] The present inventors have identified a novel Ht gene in maize that confers broad-spectrum resistance to two or more races of Exserohilum turcicum. In a particular embodiment, the gene provides resistance to any combination of at least two races of Exserohilum turcicum selected from the group consisting of race 1, race 2, race N, and race M. HtX is in the same gene cluster on chromosome 8 as Ht2 and HtN. The resistance provided by the HtX gene is additive. Homozygous configurations of HtX confer higher levels of resistance. The HtX resistance gene was identified in maize line H111 developed by the Agricultural Experiment Station of Purdue University and USDA, ARS. As described in Example 4, approximately 50% of the H111 genome is derived from dent line B37, and the remaining approximately 50% is derived from the open-pollinated population PI 209135. PI 209135 is also known as Mayorbela and is of tropical origin. Given the heterogeneous nature of PI 209135, multiple other genetically distinct lineages have been derived from this population.

[0019] The inventors have found for the first time that M1, a trait-linked SNP marker with a [C / T] change at 157,566,509 bp on chromosome 8 of the public maize B73 reference genome version 4.0 (B73 RefGen_v4), can be used to track and introgress the HtX gene into elite germplasm, and that the resistance conferred by Ht2 and HtN can be distinguished from that conferred by Ht2 and HtN, even though the Ht2 and HtN genes are in the same genomic region. The public maize reference genome is available, for example, at the Maize Genetics and Genomics Database at www.maizegdb.org, and one of skill in the art will understand that the marker sequences provided for the first time in this application can be located on any version of the public genome, including later versions. Thus, one aspect of the present invention provides sweet corn and agronomically elite corn plants comprising an introgression, the introgression comprising a chromosomal segment from Zea mays var. indentata at marker M1 (SEQ ID NO: 1).

[0020] Certain embodiments provide a corn plant comprising an introgression from Zea mays var. indentata on chromosome 8, the introgression comprising a single gene that confers broad-spectrum resistance to Exserohilum turcicum relative to a plant lacking the introgression. In further embodiments, the broad-spectrum resistance to Exserohilum turcicum is additive.

[0021] In other embodiments, the present invention provides plants comprising one or more of the novel recombinant introgressions provided herein. These novel introgressions provide robust broad-spectrum resistance to Exserohilum turcicum. In some embodiments, the broad-spectrum resistance includes resistance to multiple Exserohilum turcicum races. In further embodiments, the broad-spectrum resistance includes resistance to Exserohilum turcicum races 1, 2, M, and N. Methods of producing the plants described herein are further provided.

[0022] The present invention further provides novel trait-linked markers that can be used to generate corn plants containing the novel introgressions on chromosome 8 that confer broad-spectrum resistance to Exserohilum turcicum, as described herein. In one particular embodiment, the present invention provides trait-linked marker M1 (SEQ ID NO:1).

[0023] Further provided is a method of producing a plant comprising a chromosome segment from Zea mays var. indentata as described herein. In some examples, donor DNA from a resistant donor parent is introgressed into a corn line (a recurrent parent line). M1 (SEQ ID NO: 1) is used to select for alleles of the resistant donor parent.

[0024] In certain embodiments, the present invention provides methods for producing or selecting a corn plant exhibiting improved resistance to Exserohilum turcicum, comprising: a) crossing a corn plant provided herein with itself or with a second corn plant of a different genotype to produce one or more progeny plants; and b) selecting a progeny plant comprising the introgression. In some embodiments, the methods of the present invention comprise selecting a progeny plant by detecting a nucleic acid comprising the marker locus M1 (SEQ ID NO:1).

[0025] Because it can be difficult to cross genetically diverse plant lines, introgressing Exserohilum turcicum resistance alleles into cultivated lines using traditional breeding methods can require prohibitively large segregating populations for progeny screening with uncertain results. Therefore, marker-assisted selection (MAS) is essential to effectively introgress Exserohilum turcicum resistance alleles into elite cultivars. This was previously complicated by the inability to distinguish specific regions associated with disease resistance. For the first time, the present invention enables effective MAS by providing improved and validated markers for detecting genotypes associated with disease resistance without the need to grow large populations of plants to maturity to observe the phenotype.

[0026] I. Genomic regions, alleles, and polymorphisms associated with disease resistance in corn plants Northern leaf blight (NLB) is a foliar disease caused by Exserohilum turcicum, also known as Setosphaeria turcica, which causes significant yield losses in corn crops. Exserohilum turcicum resistance loci have been identified, including Ht1, Ht2, Ht3, HtN, and HtM. Both Ht2 and HtN are present in the Exserohilum turcicum resistance gene cluster (NLB_8.1) on chromosome 8, while Ht1 is present on chromosome 2. Each of these genes confers resistance to certain Exserohilum turcicum isolates. To create corn plants with broad-spectrum and durable resistance to Exserohilum turcicum, several different resistance loci and alleles can be combined into a single corn line. By combining different loci, the plant has broad-spectrum and durable resistance. Resistance is likely to be persistent because the pathogen is unlikely to evolve to overcome multiple resistance modes. The present invention provides a novel introgression of one or more alleles associated with broad-spectrum resistance to Exserohilum turcicum in corn plants, together with polymorphic nucleic acids and linked markers for tracking the introgression during plant breeding.

[0027] Maize lines that exhibit Exserohilum turcicum resistance are known in the art and can be used with the novel trait-linked markers provided herein according to certain embodiments of the present invention. For example, line H111, also designated PI 550527, can be used as a source of Exserohilum turcicum resistance. This source is available at the US National Plant Germplasm System and the North Central Plant Introduction Station in Ames, Iowa, USA. In addition, seeds deposited under ATCC accession number PTA-125393 can be used as a source of resistance trait.

[0028] Using the improved genetic markers and assays of the present invention, the inventors have been able to successfully identify novel introgressions from Zea mays var. indentata that confer broad-spectrum resistance to Exserohilum turcicum in plants. In one particular embodiment, the present invention provides a sweet corn plant that contains Zea mays var. indentata DNA at the marker locus M1 (SEQ ID NO: 1) on chromosome 8. In other embodiments, the present invention provides any type of agronomic elite corn plant that contains this marker locus and the associated broad-spectrum resistance to Exserohilum turcicum.

[0029] The novel introgressions provided herein confer broad-spectrum resistance to Exserohilum turcicum without the need to combine multiple race-specific resistance loci. Thus, the present invention represents a significant advance in the art.

[0030] II. Introgression of genomic regions associated with Exserohilum turcicum resistance Marker-assisted introgression involves the transfer of a chromosomal region defined by one or more markers from a first genetic background to a second genetic background. Progeny of the cross containing the introgressed genomic region can be identified by a combination of markers characteristic of the desired introgressed genomic region from the first genetic background and linked and unlinked markers characteristic of the second genetic background.

[0031] The present invention provides novel and precise markers for identifying and tracking the introgression of one or more genomic regions disclosed herein from Exserohilum turcicum resistant plants into sweet corn lines. The present invention further provides markers for identifying and tracking the novel introgressions disclosed herein during plant breeding, including marker M1.

[0032] Markers within or linked to any of the genomic intervals of the present invention may be useful in various breeding efforts, including the introgression of genomic regions associated with disease resistance into a desired genetic background. For example, markers within 40 cM, 20 cM, 15 cM, 10 cM, 5 cM, 2 cM, or 1 cM of markers associated with disease resistance described herein can be used for marker-assisted introgression of genomic regions associated with disease resistance phenotypes.

[0033] Also provided are corn plants comprising one or more introgression regions associated with a desired phenotype, with at least 10%, 25%, 50%, 75%, 90%, or 99% of the remaining genomic sequence bearing markers characteristic of the recurrent parent germplasm.Also provided are sweet corn plants comprising the introgression regions provided herein, which include regions closely linked to or adjacent to genomic regions and markers associated with a disease resistance phenotype.

[0034] III. Development of disease-resistant maize varieties For most breeding purposes, commercial breeders work with germplasm that is "cultivated," "cultivated type," or "elite." As used herein, "elite" or "cultivated" varieties refer to varieties that have resulted from breeding and selection for superior agronomic performance for use in agriculture. This includes parents of hybrid varieties that can be cultivated, as well as varieties that are cultivated themselves. These cultivated lines can be used as recurrent parents in breeding, or as sources of recurrent parent alleles. Cultivated or elite germplasm is easier to breed because it generally performs well when evaluated for horticultural performance. Many cultivated sweet corn types have been developed and are known in the art as being agronomically elite and suitable for commercial cultivation. However, the performance advantages that cultivated germplasm offers may be offset by a lack of allelic diversity. Breeders generally accept this trade-off because progress can be made more quickly working with cultivated material than when breeding with genetically diverse sources.

[0035] In contrast, when cultivated germplasm is crossed with non-cultivated germplasm, breeders can take advantage of novel alleles from the non-cultivated type. Non-cultivated germplasm may be used as a source of donor alleles in breeding. However, this approach generally poses great challenges due to fertility issues associated with crossing between diverse lines and negative linkage disorders from the non-cultivated parent. In maize plants, non-cultivated plant types can provide alleles associated with disease resistance. However, these non-cultivated types may have poor horticultural quality, such as certain deleterious traits or susceptibility to diseases.

[0036] Maize or corn plants referred to herein refer to any plant selected from the genus Zea, including but not limited to plants selected from the species Zea mays. In further embodiments, the plant can be selected from the subspecies Zea mays L. ssp. Mays, such as Zea mays L. subsp. mays Indentata (also known as dent corn), Zea mays L. subsp. mays Indurata (also known as flint corn), Zea mays L. subsp. mays Saccharata (also known as sweet corn), Zea mays L. subsp. mays Amylacea (also known as flower corn), or Zea mays L. subsp. mays Everta (also known as popcorn). Zea plants include hybrids, inbreds, partially inbreds, or members of defined or undefined populations.

[0037] The process of introgressing desired resistance genes from non-cultivated lines into elite cultivated lines while avoiding problems with linkage disorder or low heritability is a long and often difficult process. Therefore, success in the placement of alleles from wild relatives strongly depends on reliable marker assays instead of minimal or abbreviated introgression and phenotypic screening without deleterious effects. Success is further defined by simplifying the genetic characteristics of key attributes so that emphasis can be placed on the genetic gain of quantitative traits such as disease resistance. The process of introgressing genomic regions from non-cultivated lines can be greatly facilitated by the availability of precise markers for marker-assisted selection (MAS).

[0038] Thus, one skilled in the art will understand that the alleles, polymorphisms, and markers provided by the present invention allow any genomic region identified herein to be tracked and introduced into any genetic background. Furthermore, the genomic regions associated with disease resistance disclosed herein can be transferred from one genotype to another and tracked using MAS. Thus, the discovery by the applicant of precise markers associated with disease resistance will facilitate the development of maize plants with beneficial phenotypes. For example, seeds can be genotyped using the markers of the present invention to select plants that contain the desired genomic region associated with disease resistance without the need to grow the plants to maturity to evaluate the phenotype. Furthermore, MAS allows the identification of plants that are homozygous or heterozygous for the desired introgression.

[0039] Interspecific crosses can result in recombination suppression and plants with low fertility or fecundity. For example, recombination suppression has been observed in the tomato nematode resistance gene Mi, the Mla and Mlg genes in barley, the Yr17 and Lr20 genes in wheat, the Run1 gene in grapevine, and the Rma gene in peanut. Meiotic recombination is essential in classical breeding because it allows the transfer of favorable alleles across genetic backgrounds, the removal of deleterious genomic fragments, and the pyramiding of genetically closely linked traits. Therefore, recombination suppression forces breeders to expand segregating populations for progeny screening to reach the desired genetic combination.

[0040] Phenotypic evaluation of large populations is time-consuming, resource-intensive, and may not be reproducible in all environments. Marker-assisted selection offers a viable alternative. Molecular assays designed to detect unique polymorphisms, such as SNPs, are versatile. However, these molecular assays may not be able to distinguish alleles within and between corn species in a single assay. Structural rearrangements of chromosomes, such as deletions, impair hybridization and extension of synthetically labeled oligonucleotides. In the case of duplication events, multiple copies are amplified in one reaction without distinction. Thus, development and validation of accurate and predictive markers is essential for the success of MAS breeding programs. The corn plants, seeds, or cells provided herein can be genetically transformed.

[0041] Many methods for plant transformation have been developed, including biological and physical plant transformation protocols. See, for example, Miki et al., "Procedures for Introducing Foreign DNA into Plants" in Methods in Plant Molecular Biology and Biotechnology, Glick and Thompson Eds., CRC Press, Inc., Boca Raton, pp. 67-88 (1993). In addition, expression vectors and in vitro culture methods for transformation of plant cells or tissues and regeneration of plants are available. See, for example, Gruber et al., "Vectors for Plant Transformation" in Methods in Plant Molecular Biology and Biotechnology, Glick and Thompson Eds., CRC Press, Inc., Boca Raton, pp. 89-119 (1993).

[0042] One method for introducing an expression vector into a plant is based on the Agrobacterium natural transformation system. See, for example, Horsch et al., A Simple and General Method for Transferring Genes into Plants. Science, 227:1229-1231 (1985). A. tumefaciens and A. rhizogenes are plant pathogenic soil bacteria that genetically transform plant cells. Descriptions of Agrobacterium vector systems and methods for Agrobacterium-mediated gene transfer are provided, for example, by U.S. Patent No. 5,563,055, which is incorporated herein by reference in its entirety.

[0043] Several methods of plant transformation, collectively referred to as direct gene transfer, have been developed as alternatives to Agrobacterium-mediated transformation. A commonly applicable method of plant transformation is microprojectile-mediated transformation, in which DNA is carried on a microprojectile surface. Expression vectors are introduced into plant tissues using a microprojectile bombardment device, which accelerates the microprojectiles to velocities of 300-600 m / s, sufficient to penetrate plant cell walls and membranes.

[0044] Another method of physically delivering DNA to plants is sonication of target cells. Alternatively, liposome and spheroplast fusion have been used to introduce expression vectors into plants. Electroporation of protoplasts and whole cells and tissues can also be used.

[0045] Following transformation of corn target tissues, expression of the selectable marker genes described above allows for the preferential selection of transformed cells, tissues, and / or plants using regeneration and selection methods well known in the art.

[0046] The above-mentioned methods for transformation will typically be used to create a transgenic variety. The transgenic variety can then be crossed with another (non-transformed or transformed) variety to create a new transgenic variety. Alternatively, the genetic trait engineered into a particular corn line using the above-mentioned transformation techniques can be transferred to another line using conventional backcrossing techniques that are well known in the plant breeding art. For example, a backcrossing approach can be used to transfer an engineered trait from a public non-elite variety to an elite variety, or from a variety that contains an exogenous gene in its genome to a variety or varieties that do not contain the gene.

[0047] Many desirable traits that can be introduced by introgression or transformation, as described herein, can also be introduced directly into plants using genome editing molecular techniques. One aspect of the invention includes plants having genomes altered by site-specific genome modification techniques.

[0048] The corn plants, seeds, or cells provided herein can be produced by one or more genome engineering techniques or can be subjected to further genome editing. For example, one or more NLB-resistant alleles can be introduced into an NLB-susceptible background. Exemplary genome engineering techniques include meganucleases, zinc finger nucleases, TALEN, and CRISPR / Cas9 systems. See, for example, Gaj et al., ZFN, TALEN, and CRISPR / Cas-based methods for genome engineering. Trends in Biotechnology, 31:397-405 (2013). Additional genome engineering techniques known to those skilled in the art are also contemplated. Techniques of site-specific genome modification include the use of enzymes such as endonucleases, recombinases, transposases, helicases, and any combination thereof. In one embodiment, the endonuclease is selected from meganuclease, zinc finger nuclease (ZFN), transcription activator-like effector nuclease (TALEN), Argonaute, and RNA-guided nuclease, such as CRISPR-associated nuclease. In another embodiment, the endonuclease is Cas9 or Cpf1.

[0049] Site-specific genome modification enzyme induces genome modification such as double-stranded DNA break (DSB) or single-stranded DNA break at the target site of genome sequence, which is then repaired by the natural process of homologous recombination (HR) or non-homologous end joining (NHEJ).Sequence modification then occurs at the break site, which may include deletion or insertion, which in the case of NHEJ leads to gene disruption, or the integration of foreign sequence by homologous recombination.These techniques can be used, for example, to modify another locus in the plant that contains the coupling event of the present invention, to modify the coupling event of the present invention, or to recreate the coupling event of the present invention in a different plant background.

[0050] IV. Marker-assisted breeding techniques Genetic markers that can be used in the practice of the present invention include, but are not limited to, restriction fragment length polymorphisms (RFLPs), amplified fragment length polymorphisms (AFLPs), simple sequence repeats (SSRs), simple sequence length polymorphisms (SSLPs), single nucleotide polymorphisms (SNPs), insertion / deletion polymorphisms (indels), variable number of tandem repeats (VNTRs), and random amplified polymorphic DNA (RAPDs), isozymes, and other markers known to those skilled in the art. The discovery and development of markers in crop plants provides the initial framework for application in marker-assisted breeding activities (U.S. Patent Application Publication Nos. 2005 / 0204780, 2005 / 0216545, 2005 / 0218305, and 2006 / 0504538). The resulting "genetic map" represents the relative positions of characterized loci (polymorphic nucleic acid markers or other loci where alleles can be identified) relative to each other.

[0051] Polymorphisms involving only a single nucleotide change can also be assayed in several ways. For example, detection can be performed by electrophoretic methods including single-strand conformation polymorphism (Orita et al. (1989) Genomics, 8(2), 271-278), denaturing gradient gel electrophoresis (Myers (1985) EPO0273085), or cleavage fragment length polymorphism (Life Technologies, Inc., Gaithersburg, MD), although DNA sequencing is widely available and it is often easier to simply sequence the amplification products directly. Once the polymorphic sequence differences are known, rapid assays can be designed for progeny testing, usually involving some version of PCR, PCR Amplification of Specific Alleles (PASA; Sommer et al., Biotechniques 12(1), 82-87, 1992), or PCR Amplification of Multiple Specific Alleles (PAMSA; Dutton and Sommer Biotechniques, 11(6), 700-7002, 1991).

[0052] Polymorphic markers serve as useful tools for assaying plants to determine the degree of line or variety identity (U.S. Pat. No. 6,207,367). These markers form the basis for determining phenotypic associations and can be used to boost genetic gains. In certain embodiments of the methods of the invention, polymorphic nucleic acids can be used to detect genotypes associated with disease resistance in corn plants, identify corn plants having genotypes associated with disease resistance, and select genotypically associated corn plants. In certain embodiments of the methods of the invention, polymorphic nucleic acids can be used to create corn plants that contain introgressed loci associated with disease resistance in their genome. In certain embodiments of the invention, polymorphic nucleic acids can be used to breed progeny corn plants that contain one or more loci associated with disease resistance.

[0053] Genetic markers may include "dominant" or "co-dominant" markers. A "co-dominant" marker indicates the presence of two or more alleles (two per diploid individual). A "dominant" marker indicates the presence of only one allele. Markers are preferably inherited co-dominantly so that the presence of both alleles at a diploid locus, or multiple alleles at a triploid or tetraploid locus, can be easily detected, and there is no environmental variation (i.e., heritability is 1). Marker genotypes usually contain two marker alleles at each locus in a diploid organism. The composition of marker alleles at each locus can be either homozygous or heterozygous. Homozygosity is the state in which both alleles at a locus are characterized by the same nucleotide sequence. Heterozygosity refers to the different states of the alleles at a locus.

[0054] Nucleic acid based analytical methods for determining the presence or absence of genetic polymorphisms (i.e., for genotyping) can be used in breeding programs for identification, selection, introgression, etc. A variety of genetic markers exist and are known to those skilled in the art for carrying out the analysis of genetic polymorphisms. Such analysis can be used to select genes, portions of genes, QTLs, alleles, or genomic regions that are linked to or associated with disease resistance in corn plants.

[0055] Nucleic acid analysis methods as used herein include, but are not limited to, PCR-based detection methods (e.g., TaqMan assay), microarray methods, mass spectrometry-based methods, and / or nucleic acid sequencing methods, including whole genome sequencing. In certain embodiments, detection of polymorphic sites in DNA, RNA, or cDNA samples can be facilitated by using nucleic acid amplification methods. Such methods specifically increase the concentration of polynucleotides that span the polymorphic site or contain sequences located distal or proximal to the site. Such amplified molecules can be easily detected by gel electrophoresis, fluorescence detection, or other means.

[0056] One method for achieving such amplification employs polymerase chain reaction (PCR) with primer pairs capable of hybridizing to proximal sequences that define the polymorphism in double-stranded form (Mullis et al. 1986 Cold Spring Harbor Symp. Quant. Biol. 51:263-273; EP 50,424; EP 84,796; EP 258,017; EP 237,362; EP 201,184; U.S. Pat. No. 4,683,202; U.S. Pat. No. 4,582,788; and U.S. Pat. No. 4,683,194). Methods for typing DNA based on mass analysis can also be used. Such methods are disclosed in U.S. Pat. Nos. 6,613,509 and 6,503,710, and references found therein.

[0057] DNA sequence polymorphisms may be identified using any of the techniques described herein, including, but not limited to, U.S. Patent Nos. 5,468,613, 5,217,863, 5,210,015, 5,876,930, 6,030,787, 6,004,744, 6,013,431, 5,595,890, 5,762,876, 5,945,283, 5,622,876, 5,762,876, 5,945,283, 5,876,930, 5,945,283 ... The polymorphisms can be detected or typed by various effective methods well known in the art, including those disclosed in US Pat. Nos. 5,468,613, 6,090,558, 5,800,944, 5,616,464, 7,312,039, 7,238,476, 7,297,485, 7,282,355, 7,270,981 and 7,250,252. However, the compositions and methods of the present invention can be used in combination with any polymorphism typing method to type polymorphisms in genomic DNA samples. These genomic DNA samples used include, but are not limited to, genomic DNA directly isolated from plants, cloned genomic DNA, or amplified genomic DNA.

[0058] For example, polymorphisms in DNA sequences can be detected by hybridization to allele-specific oligonucleotide (ASO) probes, as disclosed in U.S. Patent Nos. 5,468,613 and 5,217,863. U.S. Patent No. 5,468,613 discloses allele-specific oligonucleotide hybridization, in which single or multiple nucleotide changes in a nucleic acid sequence can be detected in a nucleic acid by a process in which the sequence containing the nucleotide changes is amplified, spotted onto a membrane, and treated with a labeled sequence-specific oligonucleotide probe.

[0059] Target nucleic acid sequences can also be detected by probe ligation methods, such as those disclosed in U.S. Pat. No. 5,800,944, in which the sequence of interest is amplified and hybridized to a probe, followed by ligation to detect a labeled portion of the probe.

[0060] Microarrays can also be used for polymorphism detection, where a set of oligonucleotide probes are assembled with overlaps to represent a single sequence, so that a difference in the target sequence at one point will cause partial probe hybridization (Borevitz et al., Genome Res. 13:513-523 2003; Cui et al., Bioinformatics 21:3852-3858 2005). In any microarray, there are expected to be multiple target sequences that may represent genes and / or non-coding regions, and each target sequence is represented by a set of overlapping oligonucleotides rather than by a single probe. This platform provides high throughput screening of multiple polymorphisms. Target sequence typing by microarray methods is disclosed in U.S. Patent Nos. 6,799,122, 6,913,879, and 6,996,476.

[0061] Other methods for detecting SNPs and indels include single base extension (SBE) methods, examples of which include, but are not limited to, those disclosed in U.S. Patent Nos. 6,004,744, 6,013,431, 5,595,890, 5,762,876, and 5,945,283.

[0062] In another method for detecting polymorphisms, SNPs and indels can be detected by the methods disclosed in U.S. Pat. Nos. 5,210,015, 5,876,930, and 6,030,787, in which an oligonucleotide probe has a 5' fluorescent reporter dye and a 3' quencher dye covalently attached to the 5' and 3' ends of the probe. When the probe is intact, the reporter dye is in close proximity to the quencher dye, suppressing the fluorescence of the reporter dye, for example, by Forster-type energy transfer. During PCR, forward and reverse primers hybridize to specific sequences of the target DNA adjacent to the polymorphism, and the hybridization probe hybridizes to the sequence containing the polymorphism in the amplified PCR product. In the next PCR cycle, a DNA polymerase with 5' → 3' exonuclease activity cleaves the probe, separating the reporter dye from the quencher dye, resulting in an increase in reporter fluorescence.

[0063] In another embodiment, one or more loci of interest can be directly sequenced using nucleic acid sequence sequencing technology. Nucleic acid sequencing methods are known in the art and include technologies provided by 454 Life Sciences (Branford, CT), Agencourt Bioscience (Beverly, MA), Applied Biosystems (Foster City, CA), LI-COR Biosciences (Lincoln, NE), NimbleGen Systems (Madison, WI), Illumina (San Diego, CA), and VisiGen Biotechnologies (Houston, TX). Such nucleic acid sequencing technologies include formats such as parallel bead arrays, sequencing by ligation, capillary electrophoresis, electronic microchips, "biochips", microarrays, parallel microchips, and single molecule arrays.

[0064] V. Additional Breeding Techniques The corn plant or seed provided herein can also be subjected to additional breeding using one or more methods known in the art, such as pedigree breeding, recurrent selection, mass selection, and mutation breeding. Pedigree breeding begins with the crossing of two genotypes, such as a corn variety containing the Exserohilum turcicum resistance gene or Exserohilum turcicum resistance allele provided herein or two combined Exserohilum turcicum resistance QTL or two combined Exserohilum turcicum resistance alleles, and another corn variety lacking such loci. If the original two parents do not provide all the desired characteristics, other sources can be included in the breeding population. In the pedigree method, superior plants are selfed and selected in successive generations. In successive generations, the heterozygous state replaces the homozygous variety as a result of self-fertilization and selection. Pedigree breeding typically involves selfing and selection for five or more successive generations: F1 to F2, F2 to F3, F3 to F4, F4 to F5, etc. After a sufficient amount of inbreeding, the successive generations serve to increase the seed of the developed variety. The developed variety can contain homozygous alleles at approximately 95% or more of its loci.

[0065] Backcrossing can be used not only to create backcross conversions, but also in combination with pedigree breeding. As mentioned above, backcrossing can be used to transfer one or more particularly desired traits from one variety, the donor parent, to a developed variety, called the recurrent parent, that has good overall agronomic characteristics but lacks one or more desired traits. However, the same procedure can be used to move the progeny to the genotype of the recurrent parent, but at the same time retain many elements of the non-recurrent parent by stopping the backcross early and proceeding with selfing and selection. For example, one corn variety can be crossed with another variety to create a first generation progeny plant. The first generation progeny plant can then be backcrossed to one of its parent varieties to create BC1 or BC2. The progeny is selfed and selected, so the newly developed variety has many attributes of the recurrent parent and also some of the desired attributes of the non-recurrent parent. This approach leverages the value and strength of the recurrent parent for use in new corn varieties.

[0066] Recurrent selection is a method used in plant breeding programs to improve a population of plants. In this method, individual plants are cross-pollinated with each other to form progeny. The progeny are grown and superior progeny are selected by any number of selection methods, including individual plants, half-sib progeny, full-sib progeny, and selfed progeny. The selected progeny are cross-pollinated with each other to form another population of progeny. This population is planted and superior plants are again selected to cross-pollinated with each other. Because recurrent selection is a cyclical process, it can be repeated as many times as necessary. The purpose of recurrent selection is to improve the traits of the population. The improved population can be used as a source of breeding material to obtain new varieties for commercial or breeding use, including the creation of synthetic lines. Synthetic lines are progeny formed by intercrossing several selected varieties.

[0067] Mass selection is another useful technique when used in conjunction with molecular marker-enhanced selection. In mass selection, seeds are selected from individuals based on phenotype or genotype. These selected seeds are then bulked and used to grow the next generation. Bulk selection involves growing a population of plants in bulk plots, which allows the plants to self-pollinate, harvest the seeds in bulk, and then use a sample of the bulk-harvested seeds to plant the next generation. In place of self-pollination, induced pollination can also be used as part of a breeding program.

[0068] Mutation breeding can also be used to introduce new traits into the corn plants or seeds provided herein. Spontaneous or artificially induced mutations can be a useful source of variability for plant breeders. The goal of artificial mutagenesis is to increase the mutation rate of a desired characteristic. Mutation rates can be increased by many different means, including temperature, long-term seed storage, tissue culture conditions, radiation (X-rays, gamma rays (e.g., Cobalt-60 or Cesium-137), neutrons (fission products of Uranium-235 in nuclear reactors), beta rays (emitted from radioisotopes such as Phosphorus-32 or Carbon-14), or ultraviolet light (2500-2900 nm)), or chemical mutagens (such as base analogs (5-bromouracil), related compounds (8-ethoxycaffeine), antibiotics (streptonigrin), alkylating agents (sulfur mustard, nitrogen mustard, epoxides, ethyleneamines, sulfates, sulfonates, sulfones, lactones), azides, hydroxylamines, nitrous acids, or acridines). Transposon- or T-DNA-based mutagenesis is also encompassed by this disclosure. Once a desired trait is observed through mutagenesis, it can then be engineered into existing genetic resources through traditional breeding techniques.

[0069] VI.Definition The following definitions are presented to more precisely define the present invention and to guide those of ordinary skill in the art in the practice of the present invention. Unless otherwise specified, terms are to be understood according to conventional usage by those of ordinary skill in the relevant art.

[0070] As used herein, "sooty leaf spot" or "NLB", or "corn sooty leaf spot" or "NCLB" refers to a plant disease caused by the fungal pathogen Exserohilum turcicum, also known as Helminthosporium turcicum and Setosphaeria turcica.

[0071] As used herein, the term "cis configuration" or "cis linkage" refers to an arrangement in which two or more alleles are linked on the same parent chromosome. The term "trans configuration" or "trans linkage" refers to an arrangement in which two or more alleles are located on different parent chromosomes.

[0072] As used herein, the terms "recombinant" or "recombined" in the context of chromosomal segments refer to recombinant DNA sequences that contain one or more genetic loci in an arrangement not found in nature, e.g., as a result of recombination events between homologous chromosomes during meiosis.

[0073] As used herein, the term "plant" includes plant cells, plant protoplasts, plant cells in tissue culture capable of regenerating sweet corn plants, plant callus, plant mass, and plant cells that are intact in a plant or plant parts such as pollen, flowers, seeds, leaves, stems, etc.

[0074] As used herein, the term "population" means a genetically heterogeneous collection of plants that share a common parental origin.

[0075] As used herein, the terms "variety" and "cultivar" refer to a group of similar plants that can be identified from other varieties within the same species by their genetic lineage and performance.

[0076] As used herein, the term "allele" refers to one of two or more alternatives of a genomic sequence at a given locus on a chromosome.

[0077] A "quantitative trait locus" (QTL) is a chromosomal location that encodes at least the first genetic locus that influences the expressibility of a phenotype.

[0078] As used herein, "marker" refers to a detectable characteristic that can be used to distinguish between organisms. Examples of such characteristics include, but are not limited to, genetic markers, biochemical markers, metabolic products, morphological characteristics, and agronomic characteristics.

[0079] As used herein, the term "phenotype" means the detectable characteristics of a cell or organism that can be influenced by gene expression.

[0080] As used herein, the term "genotype" refers to the particular allelic makeup of a plant.

[0081] As used herein, an "elite" or "cultivated" variety means any variety that has resulted from breeding and selection for superior agronomic performance and is therefore suitable for commercial cultivation in the case of a hybrid variety, or for crossing to produce a cultivated hybrid variety. The term "cultivated" with respect to a plant or variety includes parental lines of a hybrid cultivated corn variety. An "elite plant" refers to a plant that belongs to an elite variety. Many elite varieties are available and known to those skilled in the art of corn breeding. An "elite population" is an elite individual or variety of each variety that can be used to represent the state of the art in terms of agronomically superior genotypes of a particular crop species, such as corn. Similarly, an "elite germplasm" or an elite line of germplasm is an agronomically superior germplasm.

[0082] As used herein, "agronomically elite dent corn" with respect to a plant or cultivar refers to a plant or cultivar in which at least 95% of the genome is derived from an elite dent corn cultivar as described herein above.

[0083] As used herein, the term "introgressed," when used in reference to a locus, refers to a locus that has been introduced into a new genetic background, such as by backcrossing. Introgression of a locus can be accomplished by plant breeding methods and / or molecular genetic methods. Such molecular genetic methods include, but are not limited to, various plant transformation techniques, and / or methods that provide for homologous recombination, non-homologous recombination, site-specific recombination, and / or genomic modifications that provide for locus replacement or locus conversion.

[0084] As used herein, the terms "recombinant" or "recombined" in the context of chromosomal segments refer to recombinant DNA sequences that contain one or more genetic loci in an arrangement not found in nature, e.g., as a result of recombination events between homologous chromosomes during meiosis.

[0085] As used herein, the term "linked" in the context of a nucleic acid marker and / or genomic region means that the markers and / or genomic regions are located on the same linkage group or chromosome and therefore tend to segregate together during meiosis.

[0086] As used herein, "resistance locus" refers to a locus associated with disease resistance or susceptibility. For example, the resistance locus according to the present invention, in one embodiment, can control resistance or susceptibility to Exserohilum turcicum.

[0087] As used herein, "resistance" or "improved resistance" in a plant refers to the ability of the plant to perform well, for example, by maintaining yield under disease conditions. Resistance may also refer to the ability of the plant to maintain its active phenotype under disease conditions. Resistance is a relative term, and a "resistant" plant indicates that it can maintain performance better compared to a different (less resistant) plant (e.g., a different plant variety) grown under similar disease conditions. Those skilled in the art will understand that the resistance of plants to disease conditions can vary widely and represent a spectrum of more or less resistant phenotypes. However, those skilled in the art will be able to generally determine the relative resistance of different plants, plant varieties, or plant families under disease conditions by simple observation, and will also recognize the various degrees of "resistance" phenotypes.

[0088] As used herein, "resistance" or "improved resistance" of a plant to a disease condition indicates that the plant can reduce disease load compared to a non-resistant or less resistant plant. Resistance is a relative term, and a "resistant" plant indicates that the plant can reduce disease load compared to a different (less resistant) plant (e.g., a different plant variety) grown under similar disease pressure. Those skilled in the art will understand that the resistance of a plant to a disease condition can vary widely and represent a spectrum of more or less resistant phenotypes. However, those skilled in the art will be able to generally determine the relative resistance of different plants, plant varieties, or plant families under disease conditions by simple observation, and will also recognize the various degrees of "resistance" phenotypes.

[0089] As used herein, "resistance allele" means a nucleic acid sequence associated with tolerance or resistance to a disease.

[0090] The term "about" is used to indicate that a value includes the standard deviation of error for the device or method used to determine the value. The use of the term "or" in the claims is used to mean "and / or" unless expressly indicated to refer to each alternative only or the alternatives are mutually exclusive, but the present disclosure supports the definition to refer to each alternative only and "and / or". When used in the claims with the word "comprise" or other open language, the words "a" and "an" mean "one or more" unless otherwise indicated. The terms "comprise", "have", and "include" are open-ended conjunctive verbs. Any form or tense of one or more of these verbs, such as "comprises", "comprising", "has", "having", "includes", and "including", are also open-ended. For example, any method that "comprises," "has," or "includes" one or more steps is not limited to having only those one or more steps, but also encompasses other unlisted steps. Similarly, any plant that "comprises," "has," or "includes" one or more traits is not limited to having only those one or more traits, but also encompasses other unlisted traits.

[0091] VII. Deposit Information A deposit of at least 625 seeds of sweet corn lines containing the introgressions from Zea mays var. indentata described herein has been made. The deposit was made at the American Type Culture Collection (ATCC), 10801 University Boulevard, Manassas, Va. 20110-2209 USA. The deposit was assigned ATCC deposit number PTA-125393 and was deposited on October 9, 2018. The deposit will be available upon request to qualified persons during the pendency of this application. The deposit will be maintained in the ATCC depository, a public depository, for a period of 30 years, or for 5 years from the most recent request, or for the enforceable term of the patent, whichever is longer, and will be replaced if it becomes non-viable during that period. Applicant will not tolerate any infringement of the rights granted in this patent or any other form of plant variety protection, including the Plant Variety Protection Act (7 U.S.C. 2321 et seq.). EXAMPLES

[0092] Example 1. Identification of sources of broad-spectrum resistance to Exserohilum turcicum Resistance to northern leaf spot (NLB) of corn, caused by Exserohilum turcicum, also known as Setosphaeria turcica, is conferred by both qualitative (single gene) and quantitative (multigenic) resistance. The qualitative genes of resistance to Exserohilum turcicum in corn that have been well characterized are Ht1, Ht2, Ht3, HtN, and HtM. There are known isolates of Exserohilum turcicum that can overcome each of these qualitative resistance genes. The isolates are characterized into races based on the resistance genes they can overcome. Thus, the races of Exserohilum turcicum are characterized as race 0, race 1, race 2, race 3, race N, race M, and all possible permutations thereof (e.g., race 12, race 2N, etc.), with the race number or letter indicating the Ht gene(s) to which the isolate is pathogenic. Through multiple greenhouse assays, H111 was identified as providing resistance to all races of Exserohilum turcicum. When inoculated with Exserohilum turcicum, H111 exhibits a resistant lesion type (small necrotic spots) that is distinct from resistant lesion types resulting from other known resistance genes. H111 was derived from a B37 x PI 209135 cross. PI 209135, also known as Mayorbela, is a non-elite tropical population that is well characterized for resistance to Exserohilum turcicum as well as multiple other diseases including brown spot, anthracnose, maize dwarf mosaic virus, and maize chlorotic dwarf virus. H111 was previously shown to be resistant to Exserohilum turcicum races 1 and 2. The gene HtM was reported to be present in line H102 (C123 x PI 209135) derived from PI 209135, but this gene does not confer broad-spectrum resistance to Exserohilum turcicum isolates. Thus, H111 provides a novel source of resistance to Exserohilum turcicum.

[0093] Example 2. QTL mapping of Exserohilum turcicum resistance from H111 F2-derived F3 (F2:3) families from two biparental populations were developed to map the locus conferring resistance to Exserohilum turcicum in lines H111: "Inbred 1" x H111 and "Inbred 2" x H111. "Inbred 1" and "Inbred 2" are elite sweet corn inbred lines that are fully susceptible to Exserohilum turcicum. Both populations were evaluated in replicate field trials inoculated with an Exserohilum turcicum race 2NM isolate. Parametric linkage analysis identified a single QTL on chromosome 8 spanning approximately 12 cM. This locus explained up to 97% of the observed phenotypic variance, indicating that Exserohilum turcicum resistance from H111 is conferred by a single qualitative resistance gene. Allelic effects at the QTL are primarily additive. The location of the QTL colocalizes with the known Exserohilum turcicum resistance gene cluster on chromosome 8, which also harbors the qualitative resistance genes Ht2 and HtN. Given that the population was inoculated with an Exserohilum turcicum race 2NM isolate that is virulent to Ht2, HtN, and HtM, the qualitative resistance from H111 was not conferred by Ht2, HtN, and / or HtM. Furthermore, HtM has been reported to segregate independently from Ht2 and HtN, further supporting that the resistance demonstrated by line H111 is not due to the HtM gene identified from line H102. The resistance gene from H111 is novel and was named HtX.

[0094] F3 families derived from F2 plants homozygous (resistant), susceptible or heterozygous for HtX selected from the two mapping populations were inoculated in the greenhouse with Exserohilum turcicum race 2NM and Exserohilum turcicum race 12 isolates. The presence of the HtX resistance gene explained 77-80% of the disease incidence (% of plants showing disease symptoms) in F2:3 families for both isolates. For disease incidence in the greenhouse assay, the HtX gene acted dominantly for Exserohilum turcicum race 2NM and partially dominantly for Exserohilum turcicum race 12. Using a panel of 204 sweet corn inbred lines, a trait-linked marker, M1 (SEQ ID NO:1), was developed to detect the presence of HtX, with a genetic accuracy of 99.5%. M1 contains a [C / T] change at 157,566,509 bp on chromosome 8 of the public maize B73 reference genome version 4.0 (B73 RefGen_v4), and can be used to track the trait in germplasm and distinguish it from resistance conferred by Ht2 and HtN, which are in the same genomic region.

[0095] Example 3. Efficacy of HtX in conferring broad-spectrum resistance The resistance gene HtX was introduced into two different genetic backgrounds to test its efficacy on a diverse panel of races in different locations in 2018. Co-dominance of the HtX gene was confirmed. A disease index was determined for all plants using a scale of 1 to 9. Plants with little to no infection were given a rating of 1, defined as plants with at most a few scattered lesions in the lower regions of the plant. Lightly infected plants were given a rating of 3, defined as plants with a moderate number of lesions on the lower leaves. Moderately infected plants were given a rating of 5, defined as plants with a large amount of lesions on the lower leaves and fewer lesions on the middle leaves. Heavily infected plants were given a rating of 7, defined as plants with a large amount of lesions on the lower and middle leaves and lesions spreading to the upper leaves. Very heavily infected plants were given a rating of 9, defined as plants with a large amount of lesions on all leaves and plants may have died early. It was found that a heterozygous placement of HtX results in a reduction in the disease index by 2 points on a 1-9 scale, whereas a homozygous placement reduces the disease index by an additional 2 points on average (Figure 3). Thus, plants heterozygous for HtX exhibited moderate to high resistance and were characterized by mild symptoms, whereas plants with homozygous HtX exhibited high resistance and zero to negligible disease symptoms. A disease index below 4 is considered commercially acceptable in temperate regions.

[0096] The HtX gene was introgressed in different arrangements into six additional hybrid backgrounds in 2019. These hybrids (six hybrid backgrounds × three versions of each hybrid) were tested in Florida against natural infection from Exserohilum turcicum. The six hybrid backgrounds used in this test were different from the two hybrid backgrounds tested in 2018. Although each hybrid was tested in a single run, results were pooled across hybrids to statistically analyze differences between gene arrangements. Plants heterozygous for HtX showed moderate to high resistance and were characterized by mild symptoms, whereas plants with homozygous HtX showed high resistance and zero to negligible disease symptoms, regardless of genetic background (Figure 4). Furthermore, investigations showed that in the field, races of Exserohilum turcicum were virulent to all known resistance genes except HtX. The results confirm the novel broad-spectrum resistance provided by the HtX gene and the additive mode of gene action across diverse genetic backgrounds.

[0097] The resistance conferred by the HtX gene can be stacked with the resistance traits conferred by other Ht genes. The HtX gene can be introduced into a maize plant that contains a recombinant chromosome segment containing Ht2 and Ht resistance alleles in cis configuration on chromosome 8. A coupling event between Ht2 and HtN can be created by crossing inbred lines B68HTN (carrying the HtN gene) with A619HT2 (carrying the Ht2 gene) and selecting for a recombination event between Ht2 and HtN. Both B68HTN and A619HT2 are available from the US National Plant Germplasm System. Table 1 shows markers associated with the Ht2 and HtX resistance alleles and can be used to select for recombination events. The trait-linked markers Q-NZMAY009401770 (SEQ ID NO:2) and Q-ZMHt2 (SEQ ID NO:3) are associated with the Ht2 resistance allele. The trait linked markers Q-NZMAY009238970 (SEQ ID NO: 4) and Q-NZMAY009430172 (SEQ ID NO: 5) are associated with the HtN resistance allele.

[0098] Identification of a recombinant chromosomal segment containing Ht2 and HtN resistance alleles in cis configuration on chromosome 8 and a marker associated with the recombination event is described in U.S. patent application Ser. No. 16 / 145,987, filed Sep. 28, 2018, the disclosure of which is incorporated herein by reference in its entirety. TIFF0007645183000001.tif55164

[0099] Example 4. Parent-child relationship of H111 As mentioned above, H111 was derived from a cross of B37 × PI 209135. The inheritance of parental haplotypes in H111 was estimated by analyzing 35,971 SNPs across the genome for both parental source contributions. Genomic regions with high genotypic similarity (>0.975) between B37 and H111 were assumed to indicate the inheritance of the B37 haplotype by H111. Parental recombination breakpoints and haplotype blocks could be clearly defined using this method. Based on this analysis, the regions of the chromosomes of H111 that were derived from the parental haplotype of PI 209135 were identified. The location of the HtX gene was found on chromosome 8 within a chromosomal segment inherited from PI 209135, confirming the origin of HtX from PI 209135 selected Mb.2. Overall, H111 was found to be 50% B37 in origin and 50% PI 209135-selected Mb.2, with the percentage of B37 being significantly lower than expected.

Claims

1. 1. A sweet corn plant comprising an introgression from Zea mays var. indentata on chromosome 8, said introgression comprising a single gene that confers resistance to Exserohilum turcicum relative to a plant lacking said introgression, said introgression comprising an allele from Zea mays var. indentata at marker M1 (SEQ ID NO:1) of said plant, and a sample of seed containing said introgression has been deposited under ATCC Accession No. PTA-125393.

2. 2. The plant of claim 1, wherein said resistance to Exserohilum turcicum is additive.

3. 2. The plant of claim 1, wherein the introgression is 12 cM or less.

4. 2. The plant of claim 1, wherein the resistance comprises resistance to multiple races of Exserohilum turcicum.

5. 5. The plant of claim 4, wherein the resistance comprises resistance to Exserohilum turcicum races 1, 2, M, and N.

6. The plant of claim 1 , which is homozygous for the introgression.

7. 2. The plant of claim 1, defined as an inbred or hybrid plant.

8. A plant part of the plant of claim 1.

9. 9. The plant part of claim 8, wherein the plant part is a cell, a seed, a root, a stem, a leaf, an ear, a flower, or pollen.

10. 1. An introgression fragment comprising a recombinant chromosome segment from Zea mays var. indentata at marker locus M1 (SEQ ID NO:1), wherein a sample of seeds comprising said introgression fragment has been deposited under ATCC Accession No. PTA-125393.

11. 11. The gene transfer fragment of claim 10, wherein the fragment confers resistance to Exserohilum turcicum.

12. 11. The introgression fragment of claim 10, wherein the recombinant chromosome segment from Zea mays var. indentata at marker locus M1 (SEQ ID NO:1) is flanked by genomic DNA from a sweet corn variety.

13. 1. A method for producing a sweet corn variety plant having improved resistance to Exserohilum turcicum, comprising introgressing a chromosome segment on chromosome 8 from Zea mays var. indentata into said plant, said introgression conferring resistance to Exserohilum turcicum compared to a plant lacking said introgression, said resistance being additive, said chromosome segment comprising marker locus M1 (SEQ ID NO:1), and a sample of seed comprising said chromosome segment has been deposited under ATCC Accession No. PTA-125393.

14. The gene transfer a) crossing a plant containing the chromosome segment with itself or with a second sweet corn plant of a different genotype to produce one or more progeny plants; b) selecting progeny plants containing the chromosome segment; and The method of claim 13, comprising:

15. 15. The method of claim 14, wherein selecting the progeny plant comprises detecting a nucleic acid comprising the marker locus M1 (SEQ ID NO:1).

16. 14. The method of claim 13, wherein the resistance comprises resistance to multiple races of Exserohilum turcicum.

17. 17. The method of claim 16, wherein the resistance comprises resistance to Exserohilum turcicum races 1, 2, M, and N.

18. The progeny plant is F ２ ~F ６ The method of claim 14, wherein the progeny plant is a progeny plant.

19. The method of claim 14 , wherein generating the progeny plant comprises backcrossing.

20. 14. The method of claim 13, wherein the introgressing comprises backcrossing.

21. 14. The method of claim 13, wherein the introgressing comprises marker assisted selection.

22. 14. The method of claim 13, wherein said introgression comprises assaying for said resistance to Exserohilum turcicum.

23. A plant of a sweet corn variety having improved resistance to Exserohilum turcicum, comprising an introgression of a chromosome segment on chromosome 8 from Zea mays var. indentata, said introgression conferring resistance to Exserohilum turcicum compared to a plant lacking said introgression, said resistance being additive, said chromosome segment comprising marker locus M1 (SEQ ID NO:1), and a sample of seed comprising said chromosome segment has been deposited under ATCC Accession No. PTA-125393.

24. 1. A method for selecting a sweet corn plant having improved resistance to Exserohilum turcicum, comprising: a) crossing the plant of claim 1 with itself or with a second sweet corn plant of a different genotype to produce one or more progeny plants; b) selecting progeny plants containing the introgression; and The method comprising:

25. 25. The method of claim 24, wherein selecting the progeny plant comprises detecting a marker locus genetically linked to the introgression.

26. 25. The method of claim 24, wherein selecting the progeny plant comprises detecting a nucleic acid comprising the marker locus M1 (SEQ ID NO:1).

27. 25. The method of claim 24, wherein the resistance comprises resistance to multiple races of Exserohilum turcicum.

28. 28. The method of claim 27, wherein the resistance comprises resistance to Exserohilum turcicum races 1, 2, M, and N.

29. The progeny plant is F ２ ~F ６ The method of claim 24, wherein the progeny plant is a progeny plant.

30. 25. The method of claim 24, wherein generating the progeny plant comprises backcrossing.

31. 2. The plant of claim 1, further comprising a recombinant chromosomal segment comprising a first allele comprising an Ht2 locus and a second allele comprising an HtN locus, said first allele and said second allele being arranged in cis-linkage on chromosome 8, said recombinant chromosomal segment conferring resistance to Exserohilum turcicum.

32. 32. The plant of claim 31, wherein the recombinant chromosome segment is adjacent to marker loci Q-NZMAY009401770 (SEQ ID NO:2) and Q-NZMAY009430172 (SEQ ID NO:5) on chromosome 8.

33. 33. The plant of claim 32, wherein the recombinant chromosome segment is adjacent to marker loci Q-ZMHt2 (SEQ ID NO:3) and Q-NZMAY009238970 (SEQ ID NO:4) on chromosome 8.

34. 1. A plant of an elite dent corn variety comprising an introgression from Zea mays var. indentata on chromosome 8, said introgression comprising an allele from Zea mays var. indentata at marker M1 (SEQ ID NO:1) of said plant, said introgression comprising a single gene that confers resistance to Exserohilum turcicum compared to a plant lacking said introgression, and a sample of seed comprising said introgression has been deposited under ATCC Accession No. PTA-125393.

35. 35. The plant of claim 34, wherein the resistance comprises resistance to multiple races of Exserohilum turcicum.

36. 35. The plant of claim 34, which is homozygous for the introgression.

37. 35. The plant of claim 34, wherein a sample of seed containing the introgression has been deposited under ATCC Accession No. PTA-125393.

38. 1. A method for producing a plant of an elite corn variety having improved resistance to Exserohilum turcicum, comprising introgressing a chromosome segment from Zea mays var. indentata on chromosome 8 into an elite corn variety, wherein the introgression confers resistance to Exserohilum turcicum compared to a plant lacking the introgression, the resistance being additive, the chromosome segment comprising marker locus M1 (SEQ ID NO:1), and a sample of seed comprising the chromosome segment has been deposited under ATCC Accession No. PTA-125393.

39. The gene transfer a) crossing a plant containing the chromosome segment with itself or with a second corn plant of a different genotype to produce one or more progeny plants; b) selecting progeny plants containing the chromosome segment; and 39. The method of claim 38, comprising:

40. 39. The method of claim 38, wherein selecting the progeny plant comprises detecting a nucleic acid comprising the marker locus M1 (SEQ ID NO:1).

41. 39. The method of claim 38, wherein the elite corn variety is a dent corn, a flint corn, or a sweet corn variety.

42. The progeny plant is F ２ ~F ６ The method of claim 38, which is a progeny plant.

43. A plant of an elite corn variety having improved resistance to Exserohilum turcicum, comprising an introgression of a chromosome segment from Zea mays var. indentata on chromosome 8, said introgression conferring resistance to Exserohilum turcicum compared to a plant lacking said introgression, said resistance being additive, said chromosome segment comprising marker locus M1 (SEQ ID NO:1), and a sample of seed comprising said chromosome segment has been deposited under ATCC Accession No. PTA-125393.

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