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诱导性微小RNA介导的内源性人类核纤层蛋白A/C基因敲低

Inducible microRNA-mediated knockdown of the endogenous human lamin A/C gene.

作者信息

Weidenfeld Ina

机构信息

Molecular, Cellular, and Developmental Biology, University of Colorado at Boulder, Boulder, CO 80309, USA.

出版信息

Methods Mol Biol. 2012;815:289-305. doi: 10.1007/978-1-61779-424-7_22.

Abstract

RNA interference (RNAi) enables the suppression, and hence the functional analysis, of individual genes. The use of the tetracycline (tet)-controlled transcription activation system for RNAi has become a valuable tool for conditional gene inactivation both in vitro and in vivo. Here, the generation of a conditional RNAi cell line for microRNA (miRNA)-mediated downregulation of the endogenous lamin A/C gene is described. A tet-responsive transcription unit, encoding a designed miRNA against human lamin A/C, is directly placed into a predefined genomic site of our previously developed cell line HeLa-EM2-11ht. This chromosomal locus permits the stringent control of miRNA expression, which results in the precise adjustment of lamin A/C protein concentrations. The utilization of this conditional RNAi system for the controlled inactivation of any gene of interest may significantly contribute to the study of gene functions under highly defined conditions.

摘要

RNA干扰(RNAi)能够抑制单个基因,从而实现对其功能的分析。将四环素(tet)控制的转录激活系统用于RNAi,已成为体外和体内条件性基因失活的一种有价值的工具。在此,我们描述了一种条件性RNAi细胞系的构建,该细胞系用于通过微小RNA(miRNA)介导下调内源性核纤层蛋白A/C基因。一个编码针对人核纤层蛋白A/C的设计miRNA的tet反应性转录单元,被直接插入到我们之前构建的HeLa-EM2-11ht细胞系的一个预定义基因组位点中。这个染色体位点允许对miRNA表达进行严格控制,从而精确调节核纤层蛋白A/C的蛋白质浓度。利用这种条件性RNAi系统对任何感兴趣的基因进行可控失活,可能会极大地促进在高度明确的条件下对基因功能的研究。

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