GhA0749 and GhD0744 transcription factors of upland cotton and application thereof in flowering regulation
A technology of upland cotton, positive regulation, applied in angiosperms/flowering plants, applications, chemical instruments and methods, etc., can solve problems such as unreported regulation of upland cotton functions and applications, and achieve the effect of promoting flowering
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Embodiment 1
[0030] This embodiment provides the gene sequences of upland cotton GhA0749 (GH_A07G0749) and GhD0744 (GH_D07G0744). The CDS sequence of the GhA0749 gene is shown in SEQ No. 1 in the sequence table; the CDS sequence of the GhD0744 gene is shown in SEQ No. 2 in the sequence table.
Embodiment 2
[0032] This embodiment provides upland cotton GhA0749 and GhD0744 gene cloning and vector construction methods, including:
[0033] 1. Plant material and reagent selection
[0034] The upland cotton jin668 used in the present invention, the early-maturing cotton variety Zhongmiansuo 74 and the wild-type Arabidopsis thaliana are all preserved in this laboratory and planted in the laboratory plant cultivation room and artificial climate incubator. The present invention adopts polysaccharide polyphenol plant total RNA extraction kit, rapid plasmid mini-extraction kit, and general-purpose DNA purification and recovery kit, all of which are purchased from Tiangen Biochemical Technology Co., Ltd. The reverse transcription kit Transcriptor FirstStrand cDNA Synthesis Kit and the fluorescence quantitative kit FastStart Essential DNA Green Master were purchased from Roche. Antibiotics were purchased from Solebol Corporation. Restriction enzymes were purchased from Baoriji Biotechnolog...
Embodiment 3
[0052] This example provides the application of upland cotton GhA0749 and GhD0744 genes in regulating flowering, including:
[0053] 1. Genetic transformation of Arabidopsis, VIGS silencing of upland cotton and qPCR detection
[0054] After the emergence of wild-type Arabidopsis inflorescences, use the flower dipping method to infect Arabidopsis thaliana inflorescences, and receive T 0 generation seeds. T 1 Generation of positive plants, and continue to screen in MS medium containing Kan to obtain T 2 Positive plants. When the dicotyledons of upland cotton (Zhongmian Institute 74) were flattened, VIGS upland cotton plants were obtained by injection. Quantitative fluorescence (qPCR) was used to detect the expression of target genes in transgenic Arabidopsis and VIGS upland cotton, and the relationship between GhA0749 and GhD0744 and other flowering regulatory genes was detected by qPCR. The primers used are listed in Table 2.
[0055] Table 2 Fluorescent quantitative prim...
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