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超双胸对果蝇五体不全基因的直接调控及其在果蝇中肠形态发生中的作用。

Direct regulation of decapentaplegic by Ultrabithorax and its role in Drosophila midgut morphogenesis.

作者信息

Capovilla M, Brandt M, Botas J

机构信息

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030.

出版信息

Cell. 1994 Feb 11;76(3):461-75. doi: 10.1016/0092-8674(94)90111-2.

Abstract

Drosophila homeotic genes encode transcription factors thought to control segmental identity by regulating expression of largely unknown target genes. The formation of the second midgut constriction requires the Ultrabithorax (Ubx) and abdominal-A (abd-A) homeotic genes and decapentaplegic (dpp), a gene encoding a member of the TGF beta family of proteins. We identified a 674 bp enhancer of dpp controlling its expression in the second constriction domain of the visceral mesoderm (parasegment 7). Normal enhancer function requires positive regulation by Ubx and negative regulation by abd-A. This enhancer contains UBX- and ABD-A-binding sites defined in vitro. By generating complementary alterations of the binding sites and the binding specificity of UBX, we show that Ubx directly regulates dpp expression. These regulatory interactions are relevant to normal development, because a transgene made with this enhancer driving a dpp transcription unit rescues the second midgut constriction and larval lethality phenotypes of dpps mutations.

摘要

果蝇同源异型基因编码转录因子,人们认为这些转录因子通过调节大量未知靶基因的表达来控制体节特征。中肠第二收缩环的形成需要超双胸(Ubx)和腹-A(abd-A)同源异型基因以及果蝇dpp基因,该基因编码TGF-β蛋白家族的一个成员。我们鉴定出一个674 bp的dpp增强子,它控制dpp在内脏中胚层(副节7)的第二收缩域中的表达。正常的增强子功能需要Ubx的正向调控和abd-A的负向调控。该增强子包含在体外确定的UBX和ABD-A结合位点。通过产生结合位点和UBX结合特异性的互补性改变,我们表明Ubx直接调节dpp的表达。这些调控相互作用与正常发育相关,因为用该增强子驱动dpp转录单元构建的转基因挽救了dpp突变体的中肠第二收缩环和幼虫致死表型。

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