Harada Akihito, Mallappa Chandrashekara, Okada Seiji, Butler John T, Baker Stephen P, Lawrence Jeanne B, Ohkawa Yasuyuki, Imbalzano Anthony N
Department of Advanced Medical Initiatives, JST-CREST, Faculty of Medicine, Kyushu University, Fukuoka 812-8582, Japan.
Department of Cell and Developmental Biology, University of Massachusetts Medical School, Worcester, MA 01655, USA.
Nucleic Acids Res. 2015 Feb 27;43(4):2008-21. doi: 10.1093/nar/gkv046. Epub 2015 Feb 4.
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.
在骨骼肌分化过程中,一些组织特异性基因会立即被激活,而另一些则会延迟激活。目前对控制基因时序调控的分子基础了解甚少。我们发现,尽管这些基因位于不同染色体上,但在分化的胚胎组织和分化的培养细胞中,成肌后期表达基因的调控序列而非其他区域在物理上紧密相邻。这些染色体间相互作用的形成需要谱系决定因子MyoD和功能性Brg1(SWI/SNF染色质重塑酶的ATP酶亚基)。肌细胞生成素和特定Mef2亚型的异位表达诱导了成肌分化,而未激活内源性MyoD表达。在这些条件下,晚期基因位点的调控序列并不紧密相邻,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在成肌早期限制晚期基因表达,从而有助于成肌转录的时序调控。