Department of Cellular and Molecular Medicine, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Sci Rep. 2013;3:2390. doi: 10.1038/srep02390.
While chromatin modifications can offer a useful readout for enhancer activities, it is less clear whether these modification marks are a cause or consequence of transcription factor occupancy and enhancer activation. We have examined in details the temporal events of acetyltransferase associations and histone acetylations at different regulatory regions of the Myod1 locus. Our studies demonstrate that the histone acetyltransferase (HAT) p300 is stepwise enriched at distinct Myod1 regulatory regions during myogenic differentiation. This enrichment of p300 is associated with increased histone acetylation in a discrete pattern. Inhibition of p300 HAT activity impedes myogenic differentiation, which is coupled with decreased histone acetylation at specific Myod1 regulatory regions. We show for the first time that p300 is directly involved in the early regulation of Myod1 enhancer, and provide molecular insights into how p300 HAT activity and histone acetylation are related to enhancer activation and, consequently, gene transcription.
虽然染色质修饰可以为增强子活性提供有用的读数,但这些修饰标记是转录因子占据和增强子激活的原因还是结果还不太清楚。我们详细研究了肌球蛋白重链 1 基因座(Myod1)不同调控区中乙酰转移酶关联和组蛋白乙酰化的时间事件。我们的研究表明,在成肌分化过程中,组蛋白乙酰转移酶(HAT)p300 逐步富集在不同的 Myod1 调控区。这种 p300 的富集与特定模式下组蛋白乙酰化的增加有关。抑制 p300 HAT 活性会阻碍成肌分化,同时伴随着特定 Myod1 调控区的组蛋白乙酰化减少。我们首次表明 p300 直接参与 Myod1 增强子的早期调控,并提供了分子见解,说明 p300 HAT 活性和组蛋白乙酰化与增强子激活以及基因转录的关系。