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在人前B细胞系Nalm-6中通过同源重组实现高效基因靶向。

Highly proficient gene targeting by homologous recombination in the human pre-B cell line Nalm-6.

作者信息

Adachi Noritaka, Kurosawa Aya, Koyama Hideki

机构信息

Kihara Institute for Biological Research, Yokohama City University, Yokohama, Japan.

出版信息

Methods Mol Biol. 2008;435:17-29. doi: 10.1007/978-1-59745-232-8_2.

Abstract

Gene targeting provides a powerful means for studying gene function by a reverse genetic approach. Despite recent rapid progress in gene knockdown technologies, gene knockout studies using human somatic cells will be of greater importance for analyzing the functions of human genes in greater detail. Although the frequency of gene targeting is typically very low in human cultured cells, we have recently shown that a human precursor B cell line, Nalm-6, exceptionally allows for high-efficiency gene targeting by homologous recombination. In addition, we have developed a quick and simplified method to construct gene-targeting vectors, which is applicable to all sequenced organisms as well as embryonic stem cells. The combination of the simplified vector construction technology and the highly efficient gene-knockout system using Nalm-6 cells has enabled us to disrupt virtually any locus of the human genome within one month. Our system will greatly facilitate gene-knockout studies in human cells.

摘要

基因打靶提供了一种通过反向遗传学方法研究基因功能的强大手段。尽管基因敲低技术最近取得了快速进展,但使用人类体细胞进行的基因敲除研究对于更详细地分析人类基因的功能将具有更重要的意义。虽然在人类培养细胞中基因打靶的频率通常非常低,但我们最近发现一种人类前体B细胞系Nalm-6能够通过同源重组实现高效的基因打靶。此外,我们开发了一种快速且简化的构建基因打靶载体的方法,该方法适用于所有已测序的生物体以及胚胎干细胞。简化的载体构建技术与使用Nalm-6细胞的高效基因敲除系统相结合,使我们能够在一个月内几乎敲除人类基因组的任何位点。我们的系统将极大地促进人类细胞中的基因敲除研究。

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