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CHAMP,一种由MEF2C调控的新型心脏特异性解旋酶。

CHAMP, a novel cardiac-specific helicase regulated by MEF2C.

作者信息

Liu Z P, Nakagawa O, Nakagawa M, Yanagisawa H, Passier R, Richardson J A, Srivastava D, Olson E N

机构信息

Department of Molecular Biology, University of Texas Southwestern Medical Center, 6000 Harry Hines Boulevard, Dallas, Texas 75390-9148, USA.

出版信息

Dev Biol. 2001 Jun 15;234(2):497-509. doi: 10.1006/dbio.2001.0277.

Abstract

MEF2C is a MADS-box transcription factor required for cardiac myogenesis and morphogenesis. In MEF2C mutant mouse embryos, heart development arrests at the looping stage (embryonic day 9.0), the future right ventricular chamber fails to form, and cardiomyocyte differentiation is disrupted. To identify genes regulated by MEF2C in the developing heart, we performed differential array analysis coupled with subtractive cloning using RNA from heart tubes of wild-type and MEF2C-null embryos. Here, we describe a novel MEF2C-dependent gene that encodes a cardiac-restricted protein, called CHAMP (cardiac helicase activated by MEF2 protein), that contains seven conserved motifs characteristic of helicases involved in RNA processing, DNA replication, and transcription. During mouse embryogenesis, CHAMP expression commences in the linear heart tube at embryonic day 8.0, shortly after initiation of MEF2C expression in the cardiogenic region. Thereafter, CHAMP is expressed specifically in embryonic and postnatal cardiomyocytes. At the trabeculation stage of heart development, CHAMP expression is highest in the trabecular region in which cardiomyocytes have exited the cell cycle and is lowest in the proliferative compact zone. These findings suggest that CHAMP acts downstream of MEF2C in a cardiac-specific regulatory pathway for RNA processing and/or transcriptional control.

摘要

MEF2C是心脏肌生成和形态发生所需的一种MADS盒转录因子。在MEF2C突变小鼠胚胎中,心脏发育在环化阶段(胚胎第9.0天)停滞,未来的右心室腔无法形成,心肌细胞分化受到破坏。为了鉴定MEF2C在发育中的心脏中调控的基因,我们使用来自野生型和MEF2C基因敲除胚胎心脏管的RNA,进行了差异阵列分析并结合消减克隆。在此,我们描述了一个新的MEF2C依赖性基因,它编码一种心脏特异性蛋白,称为CHAMP(由MEF2蛋白激活的心脏解旋酶),该蛋白包含七个保守基序,这些基序是参与RNA加工、DNA复制和转录的解旋酶所特有的。在小鼠胚胎发育过程中,CHAMP的表达在胚胎第8.0天的线性心脏管中开始,此时心脏发生区域刚开始表达MEF2C。此后,CHAMP特异性地在胚胎期和出生后的心肌细胞中表达。在心脏发育的小梁化阶段,CHAMP在心肌细胞已退出细胞周期的小梁区域表达最高,而在增殖性致密区表达最低。这些发现表明,CHAMP在心脏特异性的RNA加工和/或转录调控途径中,作用于MEF2C的下游。

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