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将细胞外Dpp/BMP形态发生素梯度转化为反向转录梯度。

Conversion of an extracellular Dpp/BMP morphogen gradient into an inverse transcriptional gradient.

作者信息

Müller Bruno, Hartmann Britta, Pyrowolakis George, Affolter Markus, Basler Konrad

机构信息

Institut für Molekularbiologie, Universität Zürich, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland.

出版信息

Cell. 2003 Apr 18;113(2):221-33. doi: 10.1016/s0092-8674(03)00241-1.

Abstract

Morphogen gradients control body pattern by differentially regulating cellular behavior. Here, we analyze the molecular events underlying the primary response to the Dpp/BMP morphogen in Drosophila. Throughout development, Dpp transduction causes the graded transcriptional downregulation of the brinker (brk) gene. We first provide significance for the brk expression gradient by showing that different Brk levels repress distinct combinations of wing genes expressed at different distances from Dpp-secreting cells. We then dissect the brk regulatory region and identify two separable elements with opposite properties, a constitutive enhancer and a Dpp morphogen-regulated silencer. Furthermore, we present genetic and biochemical evidence that the brk silencer serves as a direct target for a protein complex consisting of the Smad homologs Mad/Medea and the zinc finger protein Schnurri. Together, our results provide the molecular framework for a mechanism by which the extracellular Dpp/BMP morphogen establishes a finely tuned, graded read-out of transcriptional repression.

摘要

形态发生素梯度通过差异调节细胞行为来控制身体模式。在此,我们分析果蝇中对Dpp/BMP形态发生素初级反应的潜在分子事件。在整个发育过程中,Dpp信号转导导致brinker(brk)基因的分级转录下调。我们首先通过表明不同的Brk水平抑制在距Dpp分泌细胞不同距离处表达的不同组合的翅基因,来证明brk表达梯度的重要性。然后我们剖析brk调控区域,并鉴定出两个具有相反特性的可分离元件,一个组成型增强子和一个Dpp形态发生素调节的沉默子。此外,我们提供了遗传和生化证据,表明brk沉默子是由Smad同源物Mad/Medea和锌指蛋白Schnurri组成的蛋白质复合物的直接靶点。总之,我们的结果为一种机制提供了分子框架,通过该机制细胞外Dpp/BMP形态发生素建立了精细调节的、分级的转录抑制读出。

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