Isolating microsatellite DNA loci

被引:742
作者
Glenn, TC
Schable, NA
机构
[1] Savannah River Ecol Lab, Aiken, SC 29803 USA
[2] Univ S Carolina, Coker Life Sci, Dept Biol Sci, Columbia, SC 29208 USA
来源
MOLECULAR EVOLUTION: PRODUCING THE BIOCHEMICAL DATA, PART B | 2005年 / 395卷
基金
美国海洋和大气管理局; 美国国家科学基金会; 美国国家卫生研究院;
关键词
D O I
10.1016/S0076-6879(05)95013-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A series of techniques are presented to construct genomic DNA libraries highly enriched for microsatellite DNA loci. The individual techniques used here derive from several published protocols but have been optimized and tested in our research laboratories as well as in classroom settings at the University of South Carolina and University of Georgia, with students achieving nearly 100% success. Reducing the number of manipulations involved has been a key to success, decreasing both the failure rate and the time necessary to isolate loci of interest. In our lab during the past 3 years alone, these protocols have been successfully used to isolate microsatellite DNA loci from at least 55 species representing three kingdoms. These protocols have made it possible to reduce the time to identify candidate loci for primer development from most eukaryotic species to as little as 1 week.
引用
收藏
页码:202 / 222
页数:21
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