核小体
染色质
RNA聚合酶Ⅱ
生物
抄写(语言学)
真核转录
转录协同调节子
细胞生物学
组蛋白甲基化
遗传学
组蛋白密码
组蛋白
DNA
染色质重塑
发起人
基因
基因表达
DNA甲基化
语言学
哲学
作者
François Robert,Célia Jeronimo
标识
DOI:10.1016/j.tibs.2023.08.003
摘要
Eukaryotic transcription occurs on chromatin, where RNA polymerase II encounters nucleosomes during elongation. These nucleosomes must unravel for the DNA to enter the active site. However, in most transcribed genes, nucleosomes remain intact due to transcription-coupled chromatin assembly mechanisms. These mechanisms primarily involve the local reassembly of displaced nucleosomes to prevent (epi)genomic instability and the emergence of cryptic transcription. As a fail-safe mechanism, cells can assemble nucleosomes de novo, particularly in highly transcribed genes, but this may result in the loss of epigenetic information. This review examines transcription-coupled chromatin assembly, with an emphasis on studies in yeast and recent structural studies. These studies shed light on how elongation factors and histone chaperones coordinate to enable nucleosome recycling during transcription.
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