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Global transcriptional regulation of the locus encoding the skeletal muscle determination genes Mrf4 and Myf5

机译:编码骨骼肌决定基因Mrf4和Myf5的基因座的全局转录调控

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摘要

The linked Mrf4 and Myf5 genes encode two transcription factors essential for the determination and differentiation of skeletal muscle in the embryo. The locus is controlled by a multitude of interdigitated enhancers that activate gene expression at different times and in precisely defined progenitor cell populations. Manipulation of the enhancer–promoter composition of the locus reveals a novel mechanism for the regulation of such a gene cluster. Enhancers, promoters, and a new class of elements we call transcription balancing sequences, which can act as cryptic promoters, exist in a series of equilibria to ensure that enhancers and promoters together produce the highly dynamic and exquisitely specific expression patterns of the two genes. The proposed model depends upon nonproductive interactions between enhancers and both minimal and cryptic promoters, and is distinct from those developed for the β-globin and Hox clusters. Moreover, it provides an explanation for the unexpected phenotypes of the three Mrf4 knockout alleles.
机译:链接的Mrf4和Myf5基因编码两个转录因子,这些转录因子对于确定和区分胚胎中的骨骼肌至关重要。该基因座由在不同时间和精确定义的祖细胞群中激活基因表达的多个交叉指增强子控制。操纵基因的增强子-启动子组成揭示了调节这种基因簇的新机制。增强子,启动子和我们称为转录平衡序列的一类新元件,可以充当隐性启动子,它们存在一系列平衡,以确保增强子和启动子共同产生这两个基因的高度动态且精美的特异性表达模式。所提出的模型取决于增强子与最小启动子和隐秘启动子之间的非生产性相互作用,并且不同于为β-珠蛋白和Hox簇开发的模型。此外,它提供了三个Mrf4基因敲除等位基因的意外表型的解释。

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