Role of CtBP in transcriptional repression by the Drosophila giant protein

被引:31
作者
Strunk, B [1 ]
Struffi, P [1 ]
Wright, K [1 ]
Pabst, B [1 ]
Thomas, J [1 ]
Qin, L [1 ]
Arnosti, DN [1 ]
机构
[1] Michigan State Univ, Dept Biochem & Mol Biol, E Lansing, MI 48824 USA
关键词
giant; CtBP; transcriptional repression; Kruppel; even-skipped;
D O I
10.1006/dbio.2001.0454
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The giant protein is a short-range transcriptional repressor that refines the expression pattern of gap and pair-rule genes in the Drosophila blastoderm embryo. Short-range repressors including knirps, Kruppel , and snail utilize the CtBP cofactor for repression, but it is not known whether a functional interaction with CtBP is a general property of all short-range repressors. We studied giant repression activity in a CtBP mutant and find that this cofactor is required for giant repression of some, but not all, genes. While targets of giant such as the even-skipped stripe 2 enhancer and a synthetic lacZ reporter show clear derepression in the CtBP mutant, another giant target, the hunchback gene, is expressed normally. A more complex situation is seen with regulation of the Kruppel gene, in which one enhancer is repressed by giant in a CtBP-dependent manner, while another is repressed in a CtBP-independent manner. These results demonstrate that giant can repress both via CtBP-dependent and CtBP-independent pathways, and that promoter context is critical for determining giant-CtBP functional interaction. To initiate mechanistic studies of the giant repression activity, we have identified a minimal repression domain within giant that encompasses residues 89-205, including an evolutionarily conserved region bearing a putative CtBP binding motif. (C) 2001 Academic Press.
引用
收藏
页码:229 / 240
页数:12
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