Institut de recherches cliniques de Montréal, 110 Avenue des Pins Ouest, Montréal, QC H2W 1R7, Canada.
Institut de recherches cliniques de Montréal, 110 Avenue des Pins Ouest, Montréal, QC H2W 1R7, Canada; Département de Médecine, Faculté de Médecine, Université de Montréal, 2900 Boul. Édouard-Montpetit, Montréal, QC, Canada.
Cell Rep. 2019 Jul 30;28(5):1206-1218.e8. doi: 10.1016/j.celrep.2019.06.097.
Genomic DNA is framed by additional layers of information, referred to as the epigenome. Epigenomic marks such as DNA methylation, histone modifications, and histone variants are concentrated on specific genomic sites, where they can both instruct and reflect gene expression. How this information is maintained, notably in the face of transcription, is not completely understood. Specifically, the extent to which modified histones themselves are retained through RNA polymerase II passage is unclear. Here, we show that several histone modifications are mislocalized when the transcription-coupled histone chaperones FACT or Spt6 are disrupted in Saccharomyces cerevisiae. In the absence of functional FACT or Spt6, transcription generates nucleosome loss, which is partially compensated for by the increased activity of non-transcription-coupled histone chaperones. The random incorporation of transcription-evicted modified histones scrambles epigenomic information. Our work highlights the importance of local recycling of modified histones by FACT and Spt6 during transcription in the maintenance of the epigenomic landscape.
基因组 DNA 被称为表观基因组的额外信息层所包围。表观遗传标记,如 DNA 甲基化、组蛋白修饰和组蛋白变体,集中在特定的基因组位点上,在这些位点上,它们既能指导基因表达,又能反映基因表达。这些信息是如何被维持的,特别是在转录过程中,还不完全清楚。具体来说,RNA 聚合酶 II 通过时修饰组蛋白本身的保留程度尚不清楚。在这里,我们表明,在酿酒酵母中破坏转录偶联组蛋白伴侣 FACT 或 Spt6 时,几种组蛋白修饰会发生定位错误。在缺乏功能性 FACT 或 Spt6 的情况下,转录会导致核小体丢失,而这种丢失部分可以通过非转录偶联组蛋白伴侣活性的增加来补偿。转录逐出的修饰组蛋白的随机掺入打乱了表观基因组信息。我们的工作强调了在维持表观基因组景观过程中,FACT 和 Spt6 在转录过程中局部回收修饰组蛋白的重要性。