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定向诱导基因组局部突变技术:实用的单核苷酸突变发现方法

TILLING: practical single-nucleotide mutation discovery.

作者信息

Comai Luca, Henikoff Steven

机构信息

Department of Biology, Box 355325, University of Washington, Seattle, WA 98195, USA.

出版信息

Plant J. 2006 Feb;45(4):684-94. doi: 10.1111/j.1365-313X.2006.02670.x.

Abstract

In the post-genomic sequencing era, an expanding portfolio of genomic technologies has been applied to the study of gene function. Reverse genetics approaches that provide targeted inactivation of genes identified by sequence analysis include TILLING (for Targeting Local Lesions IN Genomes). TILLING searches the genomes of mutagenized organisms for mutations in a chosen gene, typically single base-pair substitutions. This review covers practical aspects of the technology, ranging from building the mutagenized population to mutation discovery, and discusses possible improvements to current protocols and the impact of new genomic methods for mutation discovery in relation to the future of the TILLING approach.

摘要

在后基因组测序时代,越来越多的基因组技术被应用于基因功能研究。反向遗传学方法可实现对通过序列分析鉴定出的基因进行靶向失活,其中包括TILLING(靶向诱导基因组局部突变)。TILLING技术通过在诱变生物体的基因组中搜索选定基因的突变,通常是单碱基对替换。本文综述了该技术的实际应用,从构建诱变群体到突变发现,并讨论了当前实验方案可能的改进,以及新的基因组方法对突变发现的影响与TILLING方法未来发展的关系。

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