Mutagenic insertion and chromosome engineering resource (MICER)

被引:102
作者
Adams, DJ
Biggs, PJ
Cox, T
Davies, R
van der Weyden, L
Jonkers, J
Smith, J
Plumb, B
Taylor, R
Nishijima, I
Yu, YJ
Rogers, J
Bradley, A
机构
[1] Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England
[2] Netherlands Canc Inst, NL-1066 CX Amsterdam, Netherlands
[3] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1038/ng1388
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Embryonic stem cell technology revolutionized biology by providing a means to assess mammalian gene function in vivo. Although it is now routine to generate mice from embryonic stem cells, one of the principal methods used to create mutations, gene targeting, is a cumbersome process. Here we describe the indexing of 93,960 ready-made insertional targeting vectors from two libraries. 5,925 of these vectors can be used directly to inactivate genes with an average targeting efficiency of 28%. Combinations of vectors from the two libraries can be used to disrupt both alleles of a gene or engineer larger genomic changes such as deletions, duplications, translocations or inversions. These indexed vectors constitute a public resource ( Mutagenic Insertion and Chromosome Engineering Resource; MICER) for high-throughput, targeted manipulation of the mouse genome.
引用
收藏
页码:867 / 871
页数:5
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