The Drosophila gene brinker reveals a novel mechanism of Dpp target gene regulation

被引:235
作者
Jazwinska, A
Kirov, N
Wieschaus, E
Roth, S
Rushlow, C
机构
[1] Max Planck Inst Entwicklungsbiol, D-72076 Tubingen, Germany
[2] NYU, Dept Biol, New York, NY 10003 USA
[3] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
关键词
D O I
10.1016/S0092-8674(00)80660-1
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
decapentaplegic (dpp), a Drosophila member of the TGF beta family of secreted molecules, functions as a long-range morphogen in patterning of the embryo and the adult appendages. Dpp signals via the SMAD proteins Mad and Medea. Here we show that in the absence of brinker (brk), Mad is not required for the activation of Dpp target genes that depend on low levels of Dpp. brk encodes a novel protein with features of a transcriptional repressor. brk itself is negatively regulated by Dpp. Dpp signaling might relieve brk's repression of low-level target genes either by transcriptional repression of brk or by antagonizing a repressor function of brk at the target gene promoters.
引用
收藏
页码:563 / 573
页数:11
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