首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Gene Networks in Development and Evolution Special Feature Sackler Colloquium: The Caenorhabditis elegans vulva: A post-embryonic gene regulatory network controlling organogenesis
【2h】

Gene Networks in Development and Evolution Special Feature Sackler Colloquium: The Caenorhabditis elegans vulva: A post-embryonic gene regulatory network controlling organogenesis

机译:发育和进化中的基因网络专题集会Sackler座谈会:秀丽隐杆线虫:控制器官发生的胚后基因调控网络

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

The Caenorhabditis elegans vulva is an elegant model for dissecting a gene regulatory network (GRN) that directs postembryonic organogenesis. The mature vulva comprises seven cell types (vulA, vulB1, vulB2, vulC, vulD, vulE, and vulF), each with its own unique pattern of spatial and temporal gene expression. The mechanisms that specify these cell types in a precise spatial pattern are not well understood. Using reverse genetic screens, we identified novel components of the vulval GRN, including nhr-113 in vulA. Several transcription factors (lin-11, lin-29, cog-1, egl-38, and nhr-67) interact with each other and act in concert to regulate target gene expression in the diverse vulval cell types. For example, egl-38 (Pax2/5/8) stabilizes the vulF fate by positively regulating vulF characteristics and by inhibiting characteristics associated with the neighboring vulE cells. nhr-67 and egl-38 regulate cog-1, helping restrict its expression to vulE. Computational approaches have been successfully used to identify functional cis-regulatory motifs in the zmp-1 (zinc metalloproteinase) promoter. These results provide an overview of the regulatory network architecture for each vulval cell type.
机译:秀丽隐杆线虫是用于解剖指导胚胎后器官发生的基因调控网络(GRN)的优雅模型。成熟的外阴包括七种细胞类型(vulA,vulB1,vulB2,vulC,vulD,vulE和vulF),每种都有其独特的时空基因表达模式。以精确的空间模式指定这些细胞类型的机制还没有被很好地理解。使用反向遗传筛选,我们确定了外阴GRN的新组件,包括vulA中的nhr-113。几种转录因子(lin-11,lin-29,cog-1,egl-38和nhr-67)彼此相互作用并协同作用,以调节多种外阴细胞类型中的靶基因表达。例如,egl-38(Pax2 / 5/8)通过积极调节vulF特性并通过抑制与相邻vulE细胞相关的特性来稳定vulF命运。 nhr-67和egl-38调节cog-1,有助于将其表达限制在vulE中。计算方法已成功用于识别zmp-1(锌金属蛋白酶)启动子中的功能性顺式调控基序。这些结果概述了每种外阴细胞类型的监管网络架构。

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