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躯干信号通过拮抗格鲁乔介导的抑制作用来调节果蝇的末端模式形成。

Torso signalling regulates terminal patterning in Drosophila by antagonising Groucho-mediated repression.

作者信息

Paroush Z, Wainwright S M, Ish-Horowicz D

机构信息

Imperial Cancer Research Fund, London, UK.

出版信息

Development. 1997 Oct;124(19):3827-34. doi: 10.1242/dev.124.19.3827.

Abstract

Patterning of the non-segmental termini of the Drosophila embryo depends on signalling via the Torso receptor tyrosine kinase (RTK). Activation of Torso at the poles of the embryo triggers restricted expression of the zygotic gap genes tailless (tll) and huckebein (hkb). In this paper, we show that the Groucho (Gro) corepressor acts in this process to confine terminal gap gene expression to the embryonic termini. Embryos lacking maternal gro activity display ectopic tll and hkb transcription; the former leads, in turn, to lack of abdominal expression of the Krüppel and knirps gap genes. We show that torso signalling permits terminal gap gene expression by antagonising Gro-mediated repression. Thus, the corepressor Gro is employed in diverse developmental contexts and, probably, by a variety of DNA-binding repressors.

摘要

果蝇胚胎非分节末端的模式形成依赖于通过躯干受体酪氨酸激酶(RTK)进行的信号传导。胚胎两极的躯干激活会触发合子型缺口基因无尾(tll)和驼背(hkb)的限制性表达。在本文中,我们表明格鲁乔(Gro)共抑制因子在此过程中发挥作用,将末端缺口基因的表达限制在胚胎末端。缺乏母源gro活性的胚胎表现出异位的tll和hkb转录;前者进而导致克虏伯氏和无翅缺口基因在腹部的表达缺失。我们表明,躯干信号传导通过拮抗Gro介导的抑制作用来允许末端缺口基因的表达。因此,共抑制因子Gro在多种发育环境中被使用,并且可能被多种DNA结合抑制因子所利用。

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