A CREB-binding site as a target for decapentaplegic signalling during Drosophila endoderm induction

被引:111
作者
Eresh, S
Riese, J
Jackson, DB
Bohmann, D
Bienz, M
机构
[1] MRC, MOL BIOL LAB, CAMBRIDGE CB2 2QH, ENGLAND
[2] EUROPEAN MOL BIOL LAB, D-69117 HEIDELBERG, GERMANY
关键词
CREB; Dpp signalling pathway; Drosophila midgut; transcription;
D O I
10.1093/emboj/16.8.2014
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) is an extracellular signal of the transforming growth factor-beta family with multiple functions during Drosophila development. For example, it plays a key role in the embryo during endoderm induction. During this process, Dpp stimulates transcription of the homeotic genes Ultrabithorax in the visceral mesoderm and labial in the subjacent endoderm. Here, we show that a cAMP response element (CRE) from an Ultrabithorax enhancer mediates Dpp-responsive transcription in the embryonic midgut, and that endoderm expression from a labial enhancer depends on multiple CREs. Furthermore, the Drosophila CRE-binding protein dCREB-B binds to the Ultrabithorax CRE, and ubiquitous expression of a dominant-negative form of dCREB-B suppresses CRE-mediated reporter gene expression and reduces labial expression in the endoderm. Therefore, a CREB protein may act as a nuclear target, or as a partner of a nuclear target, for Dpp signalling in the embryonic midgut.
引用
收藏
页码:2014 / 2022
页数:9
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