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Transgenesis of Tol2-mediated seamlessly constructed BAC mammary gland expression vectors in Mus musculus

机译:Tol2介导的小家鼠无缝构建BAC乳腺表达载体的转基因

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摘要

Bacterial artificial chromosomes (BACs) are vectors that are capable of carrying gene fragments of up to 300 kb in size, and in theory, harbor cis-regulatory elements that are necessary for the expression of specific genes. Therefore, BACs can effectively alleviate or even eliminate the position effect induced by gene-integration, rendering these as ideal expression vectors of exogenous genes. However, the number of relevant studies involving BACs as vectors of exogenous genes are limited. In the present study, we converted the BAC regulatory region of the Mus musculus Wap gene into a mammary gland-specific expression vector. Using the galK-based positive-negative selection method, we seamlessly replaced the Wap gene in a BAC with Homo sapiens GPX3, MT2, and Luc genes while keeping the original mammary gland-specific regulatory sequence intact, without introducing any extra sequences (Loxp/Frt). To improve the efficiency of creating BAC transgenic mice, we used a Tol2 transposon system optimized for mammalian codons and eliminated 100 kb of sequence from the BAC 5' end (173 kb), which resulted in an 8.5% rate of successful gene transmission via pronuclear injection. The results of the present study indicate that seamlessly constructed BAC expression vectors can be used for the transmission of the GPX3 gene. (C) 2015 Elsevier B.V. All rights reserved.
机译:细菌人工染色体(BAC)是能够携带最大300 kb大小的基因片段的载体,并且理论上具有表达特定基因所必需的顺式调控元件。因此,BAC可以有效地减轻甚至消除基因整合引起的位置效应,使其成为外源基因的理想表达载体。但是,涉及BAC作为外源基因载体的相关研究数量有限。在本研究中,我们将小家鼠Wap基因的BAC调控区转换为乳腺特异性表达载体。使用基于galK的正负选择方法,我们用智人GPX3,MT2和Luc基因无缝替换了BAC中的Wap基因,同时保持了原始的乳腺特异性调控序列完整,而没有引入任何额外序列(Loxp / Frt)。为了提高创建BAC转基因小鼠的效率,我们使用了针对哺乳动物密码子优化的Tol2转座子系统,并从BAC 5'末端消除了100 kb的序列(173 kb),从而使通过原核的成功基因传输率达到了8.5%注射。本研究的结果表明,无缝构建的BAC表达载体可用于GPX3基因的传递。 (C)2015 Elsevier B.V.保留所有权利。

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