Gene for regulating plant height of Gossypium hirsutum, and application thereof
A kind of upland cotton and genetic technology, applied in the fields of application, genetic engineering, plant genetic improvement, etc., can solve the problem of unsatisfactory marker genes of plant height, etc., and achieve the effect of strong specificity
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Embodiment 1
[0052] 1.1 Test material
[0053] The natural population constructed in this experiment includes 355 representative upland cotton germplasm resources, of which 185 resources come from the early-maturing research group of the Cotton Research Institute of the Chinese Academy of Agricultural Sciences for many years. Germplasm Bank (Anyang, Henan). Among the 355 germplasm resources, 331 variety lines came from various cotton planting ecological regions in China, and 24 variety lines were imported germplasm resources from foreign countries (mainly the United States). According to the source of different ecological regions, the 355 germplasm resources can be divided into five groups: (1) Yellow River Basin Variety Group (YR, 162 accessions); (2) Yangtze River Basin Variety Group (YZR, 51 accessions); (3) Northwest Inland Variety Group (NW, 98 copies); (4) Liaoning Variety Group or Northern Extra Early Maturing Variety Group (LN, 20 copies) and (5) American Variety Group (of which U...
Embodiment 2
[0071] The GhAP1-D3 screened in Example 1 was subjected to VIGS verification function.
[0072] The vector construction of pCLCrVA-pCLCrVB VIGS system:
[0073] The sequences of the designed specific primers are shown in SEQ ID NO.7 and SEQ ID NO.8, specifically, GhAP1-D3V-F: AGGACAAAGCACTGCAAGAACA;
[0074] GhAP1-D3V-R:TCAAGGTGGTGGCGAATCAT.
[0075] 以该引物扩增GhAP1-D3基因的217bp基因沉默的特异片段,“AGGACAAAGCACTGCAAGAACAGAATAACATACTTGCAAAGAAGGAAAAGGAGAAAACTAATGTGGAGCAGGCACATTGGCAGCTGAACAACAATTGCCAAGATTCATCCTCCATGCTTCTGCCCCTTAACATCAGCTCCAATGGAAGGGAGAAGGAAGATAATGAAACCACCAACAGTGGCGTCTTGCTGCCATGGATGATTCGCCACCACCTTGA”,扩增产物如 Figure 5 shown. From Figure 5 It can be seen that the specificity of the primer is strong, and no other bands are amplified.
[0076] Through the Spe I (ACTAGT) and Asc I (GGCGCGCC) restriction sites, replace the sequence between the two restriction sites on the pCLCrVA vector with the C-terminal sequence of GhAP1-D3-217 to obtain pCLCrVA-GhAP1-D3 -217. Transform pCLCrV...
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