Structure of the retinal determination protein Dachshund reveals a DNA binding motif

被引:66
作者
Kim, SS
Zhang, RG
Braunstein, SE
Joachimiak, A
Cveki, A
Hegde, RS
机构
[1] Childrens Hosp Res Fdn, Div Dev Biol, Cincinnati, OH 45229 USA
[2] NYU, Med Ctr, Skirball Inst, Struct Biol Program, New York, NY 10016 USA
[3] Yeshiva Univ Albert Einstein Coll Med, Dept Ophthalmol, Bronx, NY 10461 USA
[4] Yeshiva Univ Albert Einstein Coll Med, Dept Visual Sci, Bronx, NY 10461 USA
[5] Yeshiva Univ Albert Einstein Coll Med, Dept Mol Genet, Bronx, NY 10461 USA
[6] Argonne Natl Lab, Struct Biol Ctr, Argonne, IL 60439 USA
关键词
Dachshund; development; eye; winged helix; DNA binding; crystal structure;
D O I
10.1016/S0969-2126(02)00769-4
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
The Dachshund proteins are essential components of a regulatory network controlling cell fate determination. They have been implicated in eye, limb, brain, and muscle development. These proteins cannot be assigned to any recognizable structural or functional class based on amino acid sequence analysis. The 1.65 Angstrom crystal structure of the most conserved domain of human DACHSHUND is reported here. The protein forms an alpha/beta structure containing a DNA binding motif similar to that found in the winged helix/forkhead subgroup of the helix-turn-helix family. This unexpected finding alters the previously proposed molecular models for the role of Dachshund in the eye determination pathway. Furthermore, it provides a rational framework for future mechanistic analyses of the Dachshund proteins in several developmental contexts.
引用
收藏
页码:787 / 795
页数:9
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