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Spatial re-organization of myogenic regulatory sequences temporally controls gene expression

机译:成肌调控序列的空间重组在时间上控制基因表达

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摘要

During skeletal muscle differentiation, the activation of some tissue-specific genes occurs immediately while others are delayed. The molecular basis controlling temporal gene regulation is poorly understood. We show that the regulatory sequences, but not other regions of genes expressed at late times of myogenesis, are in close physical proximity in differentiating embryonic tissue and in differentiating culture cells, despite these genes being located on different chromosomes. Formation of these inter-chromosomal interactions requires the lineage-determinant MyoD and functional Brg1, the ATPase subunit of SWI/SNF chromatin remodeling enzymes. Ectopic expression of myogenin and a specific Mef2 isoform induced myogenic differentiation without activating endogenous MyoD expression. Under these conditions, the regulatory sequences of late gene loci were not in close proximity, and these genes were prematurely activated. The data indicate that the spatial organization of late genes contributes to temporal regulation of myogenic transcription by restricting late gene expression during the early stages of myogenesis.
机译:在骨骼肌分化过程中,一些组织特异性基因的激活立即发生,而其他一些则被延迟。人们对控制时间基因调控的分子基础了解甚少。我们显示,尽管这些基因位于不同的染色体上,但是调控序列,而不是在成肌的晚期表达的基因的其他区域,在分化的胚胎组织和分化的培养细胞中却在物理上紧密接近。这些染色体间相互作用的形成需要谱系决定的MyoD和功能性Brg1,即SWI / SNF染色质重塑酶的ATPase亚基。肌生成素和特定的Mef2同工型的异位表达诱导肌源性分化,而不激活内源性MyoD表达。在这些条件下,晚期基因位点的调控序列不是很接近,并且这些基因被过早激活。数据表明,晚期基因的空间组织通过限制成肌早期的晚期基因表达来促进成肌转录的时间调控。

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