首页> 外文OA文献 >LEF1-mediated regulation of Delta-like1 links Wnt and Notch signaling in somitogenesis
【2h】

LEF1-mediated regulation of Delta-like1 links Wnt and Notch signaling in somitogenesis

机译:LEF1介导的Delta-like1调节调节Wnt和Notch信号在体发生中。

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

Wnt signaling, which is mediated by LEF1/TCF transcription factors, has been placed upstream of the Notch pathway in vertebrate somitogenesis. Here, we examine the molecular basis for this presumed hierarchy and show that a targeted mutation of Lef1, which abrogates LEF1 function and impairs the activity of coexpressed TCF factors, affects the patterning of somites and the expression of components of the Notch pathway. LEF1 was found to bind multiple sites in the Dll1 promoter in vitro and in vivo. Moreover, mutations of LEF1-binding sites in the Dll1 promoter impair expression of a Dll1–LacZ transgene in the presomitic mesoderm. Finally, the induced expression of LEF1–β-catenin activates the expression of endogenous Dll1 in fibroblastic cells. Thus, Wnt signaling can affect the Notch pathway by a LEF1-mediated regulation of Dll1.
机译:由LEF1 / TCF转录因子介导的Wnt信号转导已在脊椎动物体发生中的Notch途径的上游。在这里,我们检查这种假定的层次结构的分子基础,并表明废除LEF1功能并损害共表达的TCF因子的活性的Lef1的定向突变会影响体节的形态和Notch通路的成分表达。发现LEF1在体外和体内结合Dll1启动子中的多个位点。此外,Dll1启动子中LEF1结合位点的突变会损害早熟中胚层中Dll1-LacZ转基因的表达。最后,诱导的LEF1-β-catenin表达激活了成纤维细胞内源性Dll1的表达。因此,Wnt信号可以通过LEF1介导的Dll1调节来影响Notch通路。

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