Rice thousand kernel weight gene tgw6 mutant as well as preparation method and application thereof
A thousand-grain weight and mutant technology, applied in the field of plant biology, can solve the problems of lack of value evaluation of related mutants
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Embodiment 1
[0054] Example 1 Creation of rice thousand-grain weight gene tgw6 deletion mutant based on CRISPR / Cas9 technology
[0055](1) Design of guide RNA (guideRNA, gRNA) target sequence According to the genome sequence of the rice grain length and thousand-grain weight gene TGW6 (GenBank: AB513135.1), three gRNAs targeting the thousand-grain weight gene TGW6 were designed. The 20nt oligonucleotide gRNA target sequence is designed according to the A / G(N)20NGG sequence, and the designed gRNA target sequence is compared with the rice genome database to exclude non-specific target cutting sites. The nucleotide sequence is shown in Table 1 and figure 1 .
[0056] Table 1 Oligonucleotide sequences of gRNA targets
[0057]
[0058] (2) Construction of three-target CRISPR / Cas9-gRNA vector
[0059] Referring to the method of Ma et al. (MaX, ZhangQ, ZhuQ, LiuW, ChenY, QiuR, WangB, YangZ.2015.ArobustCRISPR / Cas9systemforconvenient, high-efficiencymultiplexgenomeeditinginmonocotanddicotplan...
Embodiment 2
[0072] (1) Agrobacterium-mediated genetic transformation of rice callus
[0073] The CRISPR / Cas9-gRNA vector assembled in Example 1 was transformed into Agrobacterium EHA105 by electric shock. PCR detection (primers: hptF: 5'-TCCGGAGCCTCCGCTCGAAGTAG-3', hptR: 5'-CTGAACTCACCGCGACGTCTGTC-3') positive clones were used to infect rice material H447 (BC of R819 / Yuzhenxiang / / R819 2 f 7 ), the infection method was carried out with reference to the method of Hiei et al. (1994), and transgenic rice plants were obtained.
[0074] (2) Extraction of rice genomic DNA and PCR detection and sequencing analysis of mutants
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