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Expression vector for transgenesis of silkworms and transgenic silkworm sustained the fifth instar larval period

机译:第五龄幼虫期蚕转基因表达载体及转基因蚕

摘要

PURPOSE: An expression vector for transgenesis of silkworms and transgenic silkworm sustained for fifth instar larval period, containing the same are provided, thereby increasing the weight and size of larvae, pupae and silkworms due to the instar larval period sustainment. CONSTITUTION: The expression vector pAcIE1-EGT for transgenesis of silkworms is produced by the steps of: (1) cloning IE1 gene of AcNPV into a vector pBluescripSK(-); (2) removing 1.3 kb HindII fragment to prepare pAcIE1; (3) inserting SV40 poly(A) site derived from animals into the vector pAcIE1; and (4) inserting EGT gene derived from BmNPV-K1 into the vector pAcIE1 under regulation of IE1 gene promoter. The transgenic silkworm sustained for fifth instar larval period is produced by inserting the recombinant expression vector pAcIE1-EGT into silkworms.
机译:用途:提供了一种用于转基因家蚕的表达载体和可维持其五龄幼虫期的转基因家蚕,该载体含有相同的表达载体,从而由于幼虫期的维持而增加了幼虫,p和蚕的重量和大小。组成:用于转基因家蚕的表达载体pAcIE1-EGT是通过以下步骤产生的:(1)将AcNPV的IE1基因克隆到载体pBluescripSK(-)中; (2)去除1.3kb的HindII片段以制备pAcIE1; (3)将来源于动物的SV40poly(A)位点插入载体pAcIE1中。 (4)在IE1基因启动子的调控下,将来自BmNPV-K1的EGT基因插入载体pAcIE1中。通过将重组表达载体pAcIE1-EGT插入到家蚕中来产生维持在第五龄幼虫期的转基因家蚕。

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