Suppr超能文献

EGF 信号依赖性调控管基因的分子机制,该基因对果蝇背腹轴形成至关重要。

Molecular mechanisms of EGF signaling-dependent regulation of pipe, a gene crucial for dorsoventral axis formation in Drosophila.

机构信息

Institute for Developmental Biology, Biocenter, University of Cologne, Zuelpicher Straße 47b, 50674, Cologne, Germany.

出版信息

Dev Genes Evol. 2012 Mar;222(1):1-17. doi: 10.1007/s00427-011-0384-2. Epub 2011 Dec 24.

Abstract

During Drosophila oogenesis the expression of the sulfotransferase Pipe in ventral follicle cells is crucial for dorsoventral axis formation. Pipe modifies proteins that are incorporated in the ventral eggshell and activate Toll signaling which in turn initiates embryonic dorsoventral patterning. Ventral pipe expression is the result of an oocyte-derived EGF signal which down-regulates pipe in dorsal follicle cells. The analysis of mutant follicle cell clones reveals that none of the transcription factors known to act downstream of EGF signaling in Drosophila is required or sufficient for pipe regulation. However, the pipe cis-regulatory region harbors a 31-bp element which is essential for pipe repression, and ovarian extracts contain a protein that binds this element. Thus, EGF signaling does not act by down-regulating an activator of pipe as previously suggested but rather by activating a repressor. Surprisingly, this repressor acts independent of the common co-repressors Groucho or CtBP.

摘要

在果蝇卵子发生过程中,磺基转移酶Pipe 在腹侧滤泡细胞中的表达对于背腹轴的形成至关重要。Pipe 修饰了被整合到腹侧卵壳中的蛋白质,激活了 Toll 信号通路,从而启动了胚胎的背腹模式形成。腹侧 pipe 的表达是卵母细胞衍生的 EGF 信号的结果,该信号下调了背侧滤泡细胞中的 pipe。对突变滤泡细胞克隆的分析表明,在果蝇中已知的下游 EGF 信号转导的转录因子都不是 pipe 调控所必需的或充分的。然而,pipe 的顺式调控区含有一个 31 个碱基对的元件,对于 pipe 的抑制是必需的,并且卵巢提取物中含有一种能结合这个元件的蛋白质。因此,EGF 信号不是通过下调以前提出的 pipe 激活物来发挥作用,而是通过激活一种抑制剂来发挥作用。令人惊讶的是,这种抑制剂的作用不依赖于常见的共抑制剂 Groucho 或 CtBP。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30aa/3291829/39cd751af214/427_2011_384_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验