Method for controlling domestic silkworm pupal stage growth
A silkworm and pupa stage technology, applied in the field of genetic engineering, to achieve the effects of increasing flexibility, prolonging the pupa stage, and prolonging the pupa stage
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Embodiment 1
[0027] Embodiment one: Bombyx mori cocoon protease gene promoter ( PDPs )control GAL 4. UAS control BmKIT 3 R Construction of transgenic binary system
[0028] 1. BmKIT3 R artificial synthesis of genes
[0029] According to the published scorpion toxin BmKIT 3 The sequence of the gene, referring to the codon preference of the silkworm, synthesized a 189 nt sequence including the start codon ATG and the stop codon TGA BmKIT 3 R The gene, specific nucleotide sequence and corresponding amino acid sequence are shown in SEQ ID No.1 and SEQ ID No.2 respectively. The synthesized sequence was cloned into pUCm-T (product of Shanghai Shenergy Biotechnology Co., Ltd.), and the recombinant plasmid pUCm-IT3R was obtained, which was confirmed to be completely consistent with the designed sequence by sequencing.
[0030] 2. Construction of effector transgene vector piggyA3GFP-ie-neo-UAS-IT3R-polyA
[0031] (1) pSK-UAS plasmid construction: using pUAST plasmid DNA (see Bra...
Embodiment 2
[0052] Example 2: Bombyx mori cocoon protease gene promoter (PDP) controls GAL4, UAS control egt Construction of transgenic binary system
[0053] The technical operation process is as follows:
[0054] 1. Construction of the activated transgenic vector pigA3GFP-ie-neo-PDP-Gal4-PA: same as Step 3 in Example 1.
[0055] 2. Construction and identification of PDP-GAL4 system: same as Step 5 of Example 1.
[0056] 3. Construction of effector transgenic vector pigA3GFP-ie-neo-UAS-EGT
[0057] (1) Construction of pSK-UAS-egt vector: Bombyx mori baculovirus (BmNPV) genomic DNA was extracted according to conventional methods. PCR upstream and downstream primers Egt-1 (SEQ ID No.17: cg c tcg ag a tga cta ttc ttt gct ggc, underlined xho Ⅰ site) and Egt-2b (SEQ ID No.18: cg g gta cc t tgg ttg cta ctg gca cat aag cgc, underlined Kpn Ⅰ site); using the BmNPV genome as a template, PCR amplification was carried out, and the 1.7 kb egt Gene fragment. Kpn I / xho After 1 double ...
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