生肌调节因子的分子生物学研究。

Molecular biology & medicine Pub Date : 1991-04-01
W D Funk, M Ouellette, W E Wright
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引用次数: 0

摘要

最近发现了一个蛋白质家族,其中每个成员都有能力在许多非肌肉细胞类型中启动肌肉分化。这些因子包括MyoD1、myogenin、myf-5和MRF4,它们彼此具有同源性,属于myc相关蛋白的一个超家族。这些调节蛋白的表达导致该家族其他成员的自激活和交叉激活,以及终端分化标记的转录激活。序列分析显示,每个蛋白质中都有一个保守的基本结构域,这是与E-box型的特定DNA序列结合和肌原性激活所必需的。保守的螺旋-环-螺旋(HLH)结构域允许这些肌肉特异性蛋白相互之间以及与无处不在的表达蛋白如E2A基因产物(E12/E47)进行同源和异源二聚化。这篇综述描述了这些肌肉调节蛋白的发现和特征,以及它们在肌肉组织确定和分化的拟议模型中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular biology of myogenic regulatory factors.

A family of proteins has recently been identified, each member of which has the capacity to initiate muscle differentiation in many non-muscle cell types. These factors, which include MyoD1, myogenin, myf-5 and MRF4, share homologies with each other and belong to a superfamily of Myc-related proteins. Expression of these regulatory proteins results in auto-activation and cross-activation of other members of the family and in the transcriptional activation of the markers of terminal differentiation. Sequence analysis has shown a conserved basic domain in each protein that is required for binding to specific DNA sequences of the E-box type and for myogenic activation. A conserved helix-loop-helix (HLH) domain allows homo- and heterodimerization of these muscle-specific proteins with each other and with ubiquitously expressed proteins such as the E2A gene products (E12/E47). This review describes the discovery and characterization of these muscle regulatory proteins and their actions in the context of proposed models for the determination and differentiation of muscle tissue.

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