Suppr超能文献

同源结构域因子Nkx2-5在小鼠心脏发育过程中控制bHLH基因eHand的左右不对称表达。

Homeodomain factor Nkx2-5 controls left/right asymmetric expression of bHLH gene eHand during murine heart development.

作者信息

Biben C, Harvey R P

机构信息

The Walter and Eliza Hall Institute of Medical Research, Royal Melbourne Hospital, Victoria, Australia.

出版信息

Genes Dev. 1997 Jun 1;11(11):1357-69. doi: 10.1101/gad.11.11.1357.

Abstract

One of the first morphological manifestations of left/right (L/R) asymmetry in mammalian embryos is a pronounced rightward looping of the linear heart tube. The direction of looping is thought to be controlled by signals from an embryonic L/R axial system. We report here that morphological L/R asymmetry in the murine heart first became apparent at the linear tube stage as a leftward displacement of its caudal aspect. Beginning at the same stage, the basic helix-loop-helix (bHLH) factor gene eHand was expressed in a strikingly left-dominant pattern in myocardium, reflecting an intrinsic molecular asymmetry. In hearts of embryos lacking the homeobox gene Nkx2-5, which do not loop, left-sided eHand expression was abolished. However, expression was unaffected in Sc1-/- hearts that loop poorly because of hematopoietic insufficiency, and was right-sided in hearts of inv/inv embryos that display situs inversus. The data predict that eHand expression is enhanced in descendants of the left heart progenitor pool as one response to inductive signaling from the L/R axial system, and that eHand controls intrinsic morphogenetic pathways essential for looping. One aspect of the intrinsic response to L/R information falls under Nkx2-5 homeobox control.

摘要

哺乳动物胚胎左右(L/R)不对称的最早形态学表现之一是线性心管明显向右环化。环化方向被认为受胚胎L/R轴系信号控制。我们在此报告,小鼠心脏的形态学L/R不对称在心脏处于线性管阶段时首次显现,表现为心管尾端向左移位。从同一阶段开始,碱性螺旋-环-螺旋(bHLH)因子基因eHand在心肌中以明显左优势模式表达,反映出内在分子不对称性。在缺乏同源盒基因Nkx2-5且不发生环化的胚胎心脏中,左侧eHand表达消失。然而,在因造血功能不全而环化不良的Sc1-/-心脏中,eHand表达未受影响,而在表现出内脏反位的inv/inv胚胎心脏中,eHand表达位于右侧。这些数据预测,作为对L/R轴系诱导信号的一种反应,eHand在左心祖细胞池的后代中表达增强,并且eHand控制着环化所必需的内在形态发生途径。对L/R信息的内在反应的一个方面受Nkx2-5同源盒控制。

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