Recombinant nucleic fragment RecCR010161 and detection primer and application thereof
A technology for recombining nucleic acids and fragments, applied in the field of molecular biology, can solve the problems of long time and low efficiency, and achieve the effect of improving rice blast resistance and improving rice blast resistance.
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Embodiment 1
[0072] Example 1 Breeding of Recombinant Plants Introduced into Blast-resistant Genomic Fragments
[0073] The materials used in this example are rice 'Luxiang 618B' and rice 'Hua 3418B'.
[0074]Rice 'Hua 3418B' has good blast resistance, and it is speculated that the region where the Pil and Pik cluster alleles of chromosome 11 play a key role in the rice blast resistance of this material.
[0075] During the breeding process of the recombinant plants, the molecular markers were used to perform prospect selection on the recombinant plants, and the adopted molecular markers for prospect selection were screened. Referring to the rice Nipponbare genome MSU / TIGR annotation version 6.1, download the DNA sequence of chromosome 11 from 27,155,000 to 28,495,000. The SSR sites in the above sequences were scanned using SSRLocator software. Primer Premier 3.0 software was used to design primers for the found SSR loci, and a total of 385 pairs of primers were designed. Through the PC...
Embodiment 2
[0085] Example 2 Determination of Homologous Recombination Fragments After Introduction of Rice Blast Resistance Genomic Fragments
[0086] In order to determine the size of the imported rice blast resistance genome fragment, the homozygous single plant of the imported fragment of 'Luxiang 618B' was sequenced for homologous recombination fragments on both sides of the target genome fragment. The recombinant nucleic acid fragment of the rice blast resistance genome contained in CR010161 was named RecCR010161.
[0087] It was preliminarily determined by the rice genome-wide breeding chip RICE60K detection results that RecCR010161 was located downstream of the SNP marker R1127353173AG.
[0088] At the same time, three samples of 'Luxiang 618B', 'Hua 3418B' and CR010161 were subjected to whole-genome sequencing using Miseq sequencing technology. The TruSeq Nano DNA LTKit (illumina) kit was used for library establishment, the Library QuantificationKit–Universal (KAPA Biosystems) k...
Embodiment 3
[0097] Example 3 Resistance Identification of 'Luxiang 618B' After Introducing the Rice Blast Resistance Genome Fragment
[0098] In order to identify the resistance effect, the new line CR010161 selected by the application, the recurrent parent 'Luxiang 618B', the rice blast resistant variety Gumei No. 4 (as a positive control), and the rice blast susceptible variety Lijiang Xintuan Heigu ( As a negative control) for indoor planting, it is cultivated to the 3-4 leaf stage and then identified by the following methods:
[0099] M15Bb-1-1, M15Bb-1-2, M15Bb-2-1, M15Bb-3-1, M15Bb-4-1, M15Bb-5-1, M15Bb- 6-1, a total of 7 rice blast strains were used as inoculation strains. The strain was stored at -20°C by the sorghum grain method. Before use, the preserved sorghum grains were taken out and activated on a potato dextrose medium (PDA) plate (PDA: 200g peeled potatoes, 20g glucose, 15g agar powder, distilled water to 1L), After cultivating under light at 28°C for 5 days, take fresh...
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