Analysis of homeodomain specificities allows the family-wide prediction of preferred recognition sites

被引:331
作者
Noyes, Marcus B. [1 ,2 ]
Christensen, Ryan G. [4 ]
Wakabayashi, Atsuya [1 ,3 ]
Stormo, Gary D. [4 ]
Brodsky, Michael H. [1 ,3 ]
Wolfe, Scot A. [1 ,2 ]
机构
[1] Univ Massachusetts, Sch Med, Program Gene Funct & Express, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Dept Mol Pharmacol & Biochem, Worcester, MA 01605 USA
[3] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA 01605 USA
[4] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
关键词
D O I
10.1016/j.cell.2008.05.023
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
We describe the comprehensive characterization of homeodomain DNA-binding specificities from a metazoan genome. The analysis of all 84 independent homeodomains from D. melanogaster reveals the breadth of DNA sequences that can be specified by this recognition motif. The majority of these factors can be organized into 11 different specificity groups, where the preferred recognition sequence between these groups can differ at up to four of the six core recognition positions. Analysis of the recognition motifs within these groups led to a catalog of common specificity determinants that may cooperate or compete to define the binding site preference. With these recognition principles, a homeodomain can be reengineered to create factors where its specificity is altered at the majority of recognition positions. This resource also allows prediction of homeodomain specificities from other organisms, which is demonstrated by the prediction and analysis of human homeodomain specificities.
引用
收藏
页码:1277 / 1289
页数:13
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