Method for improving egg laying amount of original strain of mulberry silkworm
A technology of silkworm and original species, applied in the field of genetic engineering, can solve the problems of increasing the egg production of silkworm by endogenous gene expression, and achieve the effects of avoiding potential harm, saving production cost and improving egg laying level.
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Embodiment 1
[0021] Embodiment one: silkworm vasa - like Gene promoter control GAL 4. UAS control Bmovo- 1 Construction of transgenic binary system
[0022] 1. Bmovo- 1 Cloning of gene cDNA
[0023] Bombyx mori larvae ovaries were dissected, total RNA was extracted, and total RNA was used as a template, and oligo(dT) was used as a primer to synthesize cDNA by reverse transcription, using SEQ ID No.1 ( gat atc atg ccg aaa atc ttc tgg att aag, underlined Eco RV site) and SEQ ID No.2 ( gtc gac tta att gtg tac tgg cat ggg c, underlined Sal Ⅰ site) as primers, cDNA was amplified by conventional PCR, and a specific product of 2.42 kb was recovered; the product was cloned into pMD TM 19-T (Dalian Bao Biological Co., Ltd.), obtained from pMD-Bmovo, sequenced, attached figure 1 For the sequencing results, it can be confirmed that it is consistent with the published sequence of GenBank (accession number: GU477588).
[0024] 2. Construction of effector transgene vector pigU...
Embodiment 2
[0039] Embodiment two: silkworm nanos - like gene mover control GAL 4. UAS control Bmovo- 1 Construction of transgenic binary system
[0040] 1. Construction of activating transgenic vector pignanos-Gal4
[0041] (1) Construction of the pignanos plasmid: using the silkworm genome as a template, SEQ ID No.13 (tat ccc ggg tgc ctt aca tca aag aca ta, underlined as Sma Ⅰ site) and SEQ ID No.14 (cgc aga tct ttc aat tac gaa gat gtt gct underlined as Bgl Ⅱ site) as primers, PCR amplification, recovery of 0.6 kb specific fragments, cloned into pMD TM 19-T, obtained pMD-nanos, confirmed by sequencing and published on GenBank nanos - like Gene promoter sequence (8401-9001 region of BABH01013628.1) is consistent, pMD-nanos plasmid Sma I / Bgl Ⅱ Double enzyme digestion, recovery of the promoter fragment, cloned into the same digestion piggyA3GFP vector to obtain pignanos plasmid;
[0042] (2) Construction of pignanos-Gal4 vector: pBGT1 (refer to Lukacsovich T ...
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