Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Brown planthopper resistant rice gene Bph9 as well as molecular marker and application thereof

A technology of anti-BPH and molecular markers, applied in application, genetic engineering, plant gene improvement, etc., can solve problems such as difficult operation, increased production cost, and non-target biological poisoning

Active Publication Date: 2014-03-26
WUHAN UNIV
View PDF5 Cites 45 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Since the brown planthopper outbreaks mostly occur in the mature rice filling stage, when the rice plants are growing vigorously, it is very difficult to apply insecticides to the base of the rice plants.
In fact, due to the large-scale application of chemical insecticides year after year, the resistance of brown planthoppers has doubled, making the effect of pesticide control limited.
At the same time, the use of chemical pesticides to control brown planthoppers, on the one hand, increases the production cost of farmers, and on the other hand, chemical pesticides also cause environmental and ecological problems such as poisoning of non-target organisms, environmental and food pollution, etc.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Brown planthopper resistant rice gene Bph9 as well as molecular marker and application thereof
  • Brown planthopper resistant rice gene Bph9 as well as molecular marker and application thereof
  • Brown planthopper resistant rice gene Bph9 as well as molecular marker and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0162] Example 1 Positional cloning of Bph9 gene and development of linked molecular markers

[0163] 1. Preliminary positioning results of Bph9

[0164] Bph9-containing F 2 Populations, 93-11 and Pokkali (IRGC 108921) were all from the National Crop Germplasm Conservation Center of the Institute of Crop Science, Chinese Academy of Agricultural Sciences, and used the CTAB method (Murray MG&Thompson, 1980 Rapid isolation of high-molecular-weight plant DNA.Nucleic Acids Res 8 :4321-4325) to extract parent and F 2 Genomic DNA of each individual plant in the population. each F 2 A single plant obtains the corresponding F 2:3 family lineage. To identify F 2 To locate the N. lugens resistance phenotype of each individual plant in the population, the seedling group method was used to investigate the resistance performance of each individual plant of the F2:3 family (see figure 1 ) to F 2:3 Family resistance level represents F 2 BPH-resistant phenotype of individual plants. ...

Embodiment 2

[0221] Example 2 Functional Verification and Application of Bph9 Gene

[0222] 1. Construction of Genetic Transformation Vectors

[0223] (1) Construction of transformation vectors for the Bph9 gene's own promoter, its own complete ORF, and its own transcription terminator region. The vector used was pCAMBIA1301 (purchased from the Center for the Application of Molecular Biology to International Agriculture in Australia), and the pCAMBIA1301 vector was double-digested with SalI and EcoRI to connect the foreign fragment into the SalI and EcoRI sites of pCAMBIA1301.

[0224] According to the screening and sequencing results of the Fosmid genome library, the 3026 bp fragment obtained from the Fosmid clone where the Bph9 gene is located was double-digested with SalI and NcoI as the promoter region of the Bph9 gene (the NcoI site is the translation initiation codon of the Bph9 gene).

[0225] The full-length cDNA clone of the Bph9 gene was digested with NcoI and XhoI to obtain a ...

Embodiment 3

[0234] Example 3 Verification of Molecular Markers

[0235] 1. Materials and methods

[0236] 1.1 Materials: BPH-resistant parent Pokkali (IRGC 108921, containing brown planthopper-resistant gene Bph9), brown planthopper-susceptible rice variety Yangdao 6 (93-11) and F produced by crossing Pokkali and Yangdao 6 23 The family, 93-11 and Pokkali are all from the National Crop Germplasm Conservation Center of the Institute of Crop Science, Chinese Academy of Agricultural Sciences.

[0237] Molecular marker primers: InD2, RM28466, RM28438, InD28450, InD28453, InD14, InD28432, RM28481 and RM28486, the nucleotide sequences of which are respectively shown in SEQ ID No. 4-21.

[0238] 1.2 Method

[0239]Genomic DNA was extracted from rice samples by CTAB extraction. Sample DNA was amplified with primers InD2, RM28466, RM28438, InD28450, InD28453, InD 14, InD28432, RM28481 and RM28486, respectively. 10 μl system. The 10 μl reaction system includes: 10×PCR buffer, 1.0 μl; 10 mM dNT...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention provides a brown planthopper resistant rice gene Bph9 as well as a molecular marker and application thereof. The brown planthopper resistant rice gene Bph9 has a nucleotide sequence as shown in SEQ ID No.1 and a cDNA (complementary Desoxvribose Nucleic Acid) sequence as shown in SEQ ID No.2. The Bph9 gene is located between molecular markers InD2 and RM28466. The molecular markers closely linked with the gene also includes one of RM28438, InD28450, InD28453, InD14, InD28432, RM28481 and RM28486 which can be used for sieving the rice containing the brown planthopper resistant gene Bph9. The Bph9 gene belongs to the NBS-LRR (Nucleotide Binding Site-Leucine Rich Repeat) gene family; the encoded protein is related to the plant disease resistance; the Bph9 gene is transferred into common rice by virtue of genetic transformation and hybridization, and thus the resistance of rice to brown planthopper can be improved, so that the damage of brown planthopper is decreased, and the purposes of yield increase and yield stabilization are realized.

Description

technical field [0001] The invention belongs to the field of plant genetic engineering, and specifically relates to a brown planthopper-resistant rice gene Bph9, and also relates to a molecular marker of the gene and the application of the gene and the molecular marker in breeding brown planthopper-resistant rice and rice seeds. Background technique [0002] Rice is an important food crop, which is the staple food for more than half of the world's people. At the same time, since the fine genetic map and physical map of the rice genome have been completed, its transgenic technology is relatively easy, and it has collinearity with other grass crop genomes, so it is regarded as a model plant. With the completion of genome sequencing of various organisms including rice, human beings have entered the post-genome era. It has become the frontier field of life science to carry out functional genome research in an all-round way. Therefore, the study of rice functional genes is of g...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C12N15/29C07K14/415C12N15/63C12N1/21C12N5/10C12Q1/68C12N15/82C12N15/84A01H5/00C12N15/11
CPCC07K14/415C12N15/8286Y02A40/146
Inventor 何光存陈荣智王洋荆胜利祝莉莉杜波
Owner WUHAN UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products