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利用人 Nalm-6 前 B 细胞系进行基因靶向。

Gene targeting using the human Nalm-6 pre-B cell line.

机构信息

International Graduate School of Arts and Sciences, Yokohama City University, Kanazawa-ku, Yokohama, Kanagawa, Japan.

出版信息

Biosci Trends. 2008 Oct;2(5):169-80.

Abstract

Gene targeting by homologous recombination is a powerful tool to precisely manipulate the genome in order to study the function of a gene of interest (GOI). Indeed, it has become a routine methodology in yeasts, murine embryonic stem cells, and a chicken DT40 cell line. However, gene targeting has not been used often in human somatic cells to date since the relative efficiency of gene targeting (the ratio of homologous integrations to random integrations) is remarkably low. In this review, we introduce a fundamental strategy and a protocol to generate a null allele and/or 'tetracycline-inducible conditional gene knochout' for the GOI by gene targeting in the human Nalm-6 pre-B cell line. The Nalm-6 is a rare cell line in which gene targeting by homologous recombination takes place efficiently, and it carries a stable near-diploid karyotype with a doubling time of around 20 h. In addition, the tetracycline-regulated gene depletion (Tet-Off) system is steadily applicable to this cell line. Therefore, gene targeting systems using the Nalm-6 cell are used increasingly and offer promise in the study of human gene functions. This review should prove useful to researchers in a wide rage of fields.

摘要

同源重组基因靶向是一种精确操作基因组的强大工具,用于研究感兴趣基因(GOI)的功能。事实上,它已经成为酵母、小鼠胚胎干细胞和鸡 DT40 细胞系中的常规方法。然而,迄今为止,由于基因靶向的相对效率(同源整合与随机整合的比例)非常低,因此在人类体细胞中尚未广泛应用基因靶向。在这篇综述中,我们介绍了一种基本策略和方案,通过基因靶向在人 Nalm-6 前 B 细胞系中生成 GOI 的缺失等位基因和/或“四环素诱导的条件性基因敲除”。Nalm-6 是一种稀有细胞系,其中同源重组基因靶向效率很高,并且具有稳定的近二倍体核型,倍增时间约为 20 小时。此外,四环素调控的基因缺失(Tet-Off)系统可稳定适用于该细胞系。因此,使用 Nalm-6 细胞的基因靶向系统在人类基因功能研究中得到了越来越多的应用,并具有广阔的前景。本综述应该对广泛领域的研究人员都有用。

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