Applications of protein nog1 in regulation of yield and/or kernel number of plants
A protein and grain number per ear technology, applied in the biological field, can solve the problems of narrow genetic diversity, similar genetic basis and genotype, and restricting rice yield potential.
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Embodiment 1
[0062] Embodiment 1, the discovery of nog1 gene
[0063] Using Jiangxi Dongxiang wild rice as the donor parent and Guichao 2 as the recurrent parent, a set of introgressive line populations containing 265 lines (one of which is SIL176) was constructed by crossing and backcrossing. The coverage rate of the wild rice genome in this population is 79.4%, and the yield per plant of 15 lines (one of which is SIL176) is more than 35% lower than that of Guichao 2. The morphology of the main stem panicle, the number of grains on the main stem panicle and the yield per plant of Guichao 2 and SIL176 were compared and counted. The experiment was repeated three times, with 30 plants each time.
[0064] See the experimental results figure 1 (A is the shape of the main stem and ear, bar=5cm; B is the number of grains on the main stem and ear; C is the yield per plant; ** indicates that P<0.01 is extremely significant). The results showed that compared with Guichao 2, the number of grains...
Embodiment 2
[0066] Example 2, T 2 Obtaining and phenotypic identification of homozygous RNAi interfering strains
[0067] 1. Construction of recombinant plasmid pRNAi-nog1
[0068] The construction steps of the recombinant plasmid pRNAi-nog1 are as follows:
[0069] 1. Synthetic primers
[0070] According to the sequence of the nog1 gene shown in Sequence 1 in the sequence listing, primers 860-rnai-320F, 860-rnai-681R, 860-rnai-681F and 860-rnai-314R were designed and synthesized; the primer sequences are as follows:
[0071] 860-rnai-320F: 5′-GG ACTAGT GGGAGAAAGATGAGGA-3' (the underline is the recognition site of restriction endonuclease SpeI);
[0072] 860-rnai-681R: 5′-TCC GAGCTC GGTCAAAGCCAGGTAC-3' (the underline is the restriction endonuclease SacI recognition site);
[0073] 860-rnai-681F: 5′-CG GGATCC GGTCAAAGCCAGGTAC-3' (the underline is the restriction endonuclease BamHI recognition site);
[0074] 860-rnai-314R: 5′-GG GGTAC CAGAGCTGGGAGAAAGA-3' (the underline is the...
Embodiment 3
[0103] Example 3, T 2 Generation and phenotypic identification of homozygous complementation lines
[0104] 1. Construction of recombinant plasmid pCAMBIA1300-NOG1
[0105] The construction steps of the recombinant plasmid pCAMBIA1300-NOG1 are as follows:
[0106] 1. Using the 2-week-old seedling experimental material of Guichao 2, extract genomic DNA and use it as a template, use 860HBF: 5'-GA AGATCT CATCTGATGCCTCATACTGA-3' (the underline is the restriction endonuclease BglII recognition site) and 860HBR: 5'-CCG ACGCGT CATGCTTAGGCTGTTGAT-3' (the underline is the recognition site of the restriction endonuclease MluI) was used as a primer for PCR amplification to obtain a PCR amplification product of about 7 kb.
[0107] 2. Digest the PCR amplification product with restriction endonucleases BglII and MluI, and recover the digested product.
[0108] 3. The transformed plant expression vector pCAMBIA1300 was digested with restriction endonucleases BglII and MluI, and about ...
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