首页> 美国卫生研究院文献>other >Dissecting the sharp response of a canonical developmental enhancer reveals multiple sources of cooperativity
【2h】

Dissecting the sharp response of a canonical developmental enhancer reveals multiple sources of cooperativity

机译:剖析标准发展促进剂的敏锐反应揭示了合作的多种来源

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

Developmental enhancers integrate graded concentrations of transcription factors (TFs) to create sharp gene expression boundaries. Here we examine the hunchback P2 (HbP2) enhancer which drives a sharp expression pattern in the Drosophila blastoderm embryo in response to the transcriptional activator Bicoid (Bcd). We systematically interrogate cis and trans factors that influence the shape and position of expression driven by HbP2, and find that the prevailing model, based on pairwise cooperative binding of Bcd to HbP2 is not adequate. We demonstrate that other proteins, such as pioneer factors, Mediator and histone modifiers influence the shape and position of the HbP2 expression pattern. Comparing our results to theory reveals how higher-order cooperativity and energy expenditure impact boundary location and sharpness. Our results emphasize that the bacterial view of transcription regulation, where pairwise interactions between regulatory proteins dominate, must be reexamined in animals, where multiple molecular mechanisms collaborate to shape the gene regulatory function.
机译:发育增强剂整合了渐变浓度的转录因子(TF),以创建清晰的基因表达边界。在这里,我们研究了驼背P2(HbP2)增强子,该蛋白在果蝇胚盘胚胎中响应转录激活因子Bicoid(Bcd)驱动了清晰的表达模式。我们系统地询问影响HbP2驱动的表达的形状和位置的顺式和反式因子,发现基于Bcd与HbP2的成对协同结合的普遍模型是不够的。我们证明其他蛋白质,例如先驱因子,介体和组蛋白修饰符会影响HbP2表达模式的形状和位置。将我们的结果与理论进行比较,揭示了高阶合作性和能源消耗如何影响边界位置和清晰度。我们的结果强调,必须在动物中重新检查转录调控的细菌学观点,其中调控蛋白之间的成对相互作用占主导,在动物中,多种分子机制协同作用以塑造基因调控功能。

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