首页> 美国卫生研究院文献>PLoS Genetics >A Hox Transcription Factor Collective Binds a Highly Conserved Distal-less cis-Regulatory Module to Generate Robust Transcriptional Outcomes
【2h】

A Hox Transcription Factor Collective Binds a Highly Conserved Distal-less cis-Regulatory Module to Generate Robust Transcriptional Outcomes

机译:Hox转录因子集体绑定一个高度保守的远端无顺式调节模块以生成可靠的转录结果。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

cis-regulatory modules (CRMs) generate precise expression patterns by integrating numerous transcription factors (TFs). Surprisingly, CRMs that control essential gene patterns can differ greatly in conservation, suggesting distinct constraints on TF binding sites. Here, we show that a highly conserved Distal-less regulatory element (DCRE) that controls gene expression in leg precursor cells recruits multiple Hox, Extradenticle (Exd) and Homothorax (Hth) complexes to mediate dual outputs: thoracic activation and abdominal repression. Using reporter assays, we found that abdominal repression is particularly robust, as neither individual binding site mutations nor a DNA binding deficient Hth protein abolished cooperative DNA binding and in vivo repression. Moreover, a re-engineered DCRE containing a distinct configuration of Hox, Exd, and Hth sites also mediated abdominal Hox repression. However, the re-engineered DCRE failed to perform additional segment-specific functions such as thoracic activation. These findings are consistent with two emerging concepts in gene regulation: First, the abdominal Hox/Exd/Hth factors utilize protein-protein and protein-DNA interactions to form repression complexes on flexible combinations of sites, consistent with the TF collective model of CRM organization. Second, the conserved DCRE mediates multiple cell-type specific outputs, consistent with recent findings that pleiotropic CRMs are associated with conserved TF binding and added evolutionary constraints.
机译:顺式调控模块(CRM)通过整合众多转录因子(TF)生成精确的表达模式。出乎意料的是,控制基本基因模式的CRM的保守性可能大不相同,这表明对TF结合位点的独特限制。在这里,我们显示了控制腿前体细胞中基因表达的高度保守的无远端调控元件(DCRE)募集了多个Hox,Edententicle(Exd)和Homothorax(Hth)复合物来介导双重输出:胸腔激活和腹部抑制。使用报告基因检测,我们发现腹部抑制作用特别强大,因为单个结合位点突变和DNA结合缺陷型Hth蛋白都不能消除协同DNA结合和体内抑制作用。此外,包含Hox,Exd和Hth位点独特结构的重新设计的DCRE也介导了腹部Hox抑制。但是,重新设计的DCRE无法执行其他特定于段的功能,例如胸腔激活。这些发现与基因调节中的两个新兴概念一致:首先,腹部Hox / Exd / Hth因子利用蛋白质-蛋白质和蛋白质-DNA相互作用在灵活的位点组合上形成阻抑复合物,与CRM组织的TF集体模型一致。第二,保守的DCRE介导了多种细胞类型的特异性输出,这与最近发现的多效CRM与保守的TF结合和增加的进化限制相关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号