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通过RecA介导的克隆发现基因家族和可变剪接变体。

Discovery of gene families and alternatively spliced variants by RecA-mediated cloning.

作者信息

Zeng Hong, Allen Elizabeth, Lehman Chris W, Sargent R Geoffrey, Pati Sushma, Zarling David A

机构信息

Pangene Corporation, 5500 Stewart Avenue, Fremont, California, 94538, USA.

出版信息

Genomics. 2002 Nov;80(5):543-51.

Abstract

Probing the functional complexity of the human genome will require new gene cloning techniques, not only to discover intraspecies gene homologs and interspecies gene orthologs, but also to identify alternatively spliced gene variants. We report homologous cDNA cloning methods that allow cloning of gene family members, genes from different species, and alternatively spliced gene variants. We cloned human 14-3-3 gene family members using DNA probes with as much as 35% sequence divergence, cloned alternatively spliced gene forms of Rad51D, and cloned a novel splice form of the human 14-3-3 theta gene with a unique expression pattern. Interspecies gene cloning was demonstrated for the mouse Rad51C and mouse beta-actin genes using human gene probes. The gene family cloning method is fast, efficient, and free from PCR errors; moreover, it exploits the abilities of RecA protein to pair homologous or partially homologous DNA sequences stably in kinetically trapped, multistranded DNA hybrids that can be used for subsequent gene clone enrichment.

摘要

探究人类基因组的功能复杂性需要新的基因克隆技术,这不仅是为了发现种内基因同源物和种间基因直系同源物,也是为了识别可变剪接的基因变体。我们报道了同源cDNA克隆方法,该方法能够克隆基因家族成员、来自不同物种的基因以及可变剪接的基因变体。我们使用序列差异高达35%的DNA探针克隆了人类14-3-3基因家族成员,克隆了Rad51D的可变剪接基因形式,并克隆了具有独特表达模式的人类14-3-3θ基因的一种新型剪接形式。利用人类基因探针成功实现了小鼠Rad51C和小鼠β-肌动蛋白基因的种间基因克隆。该基因家族克隆方法快速、高效且无PCR错误;此外,它利用了RecA蛋白在动力学捕获的多链DNA杂交体中稳定配对同源或部分同源DNA序列的能力,这些杂交体可用于后续基因克隆富集。

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