Large-scale discovery of induced point mutations with high-throughput TILLING

被引:370
作者
Till, BJ
Reynolds, SH
Greene, EA
Codomo, CA
Enns, LC
Johnson, JE
Burtner, C
Odden, AR
Young, K
Taylor, NE
Henikoff, JG
Comai, L
Henikoff, S
机构
[1] Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
[2] Univ Washington, Dept Biol, Seattle, WA 98195 USA
[3] Howard Hughes Med Inst, Coconut Grove, FL 33133 USA
关键词
D O I
10.1101/gr.977903
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
TILLING ((T) under bar argeting (I) under bar nduced (L) under bar ocal (L) under bar esions in (G) under bar enomes) is a general reverse-genetic strategy that provides an allelic series of induced point mutations in genes of interest. High-throughput TILLING allows the rapid and low-cost discovery of induced point mutations in populations of chemically mutagenized individuals. As chemical mutagenesis is widely applicable and mutation detection for TILLING is dependent only on sufficient yield of PCR products, TILLING can be applied to most organisms. We have developed TILLING as a service to the Arabidopsis community known as the Arabidopsis TILLING Project (ATP). Our goal is to rapidly deliver allelic series of ethylmethanesulfonate-induced mutations in target 1-kb loci requested by the international research community. In the first year of public operation, ATP has discovered, sequenced, and delivered >1000 mutations in >100 genes ordered by Arabidopsis researchers. The tools and methodologies described here can be adapted to create similar facilities for other organisms.
引用
收藏
页码:524 / 530
页数:7
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