Laboratory of Biochemistry & Molecular Biology, National Cancer Institute, NIH, Bethesda, United States.
Laboratory of Cell Biology, National Cancer Institute, NIH, Bethesda, United States.
Elife. 2022 Mar 16;11:e75475. doi: 10.7554/eLife.75475.
Condensins compact chromosomes to promote their equal segregation during mitosis, but the mechanism of condensin engagement with and action on chromatin is incompletely understood. Here, we show that the general transcription factor TFIIH complex is continuously required to establish and maintain a compacted chromosome structure in transcriptionally silent egg extracts. Inhibiting the DNA-dependent ATPase activity of the TFIIH complex subunit XPB rapidly and reversibly induces a complete loss of chromosome structure and prevents the enrichment of condensins I and II, but not topoisomerase II, on chromatin. In addition, inhibiting TFIIH prevents condensation of both mouse and nuclei in egg extracts, which suggests an evolutionarily conserved mechanism of TFIIH action. Reducing nucleosome density through partial histone depletion restores chromosome structure and condensin enrichment in the absence of TFIIH activity. We propose that the TFIIH complex promotes mitotic chromosome condensation by dynamically altering the chromatin environment to facilitate condensin loading and condensin-dependent loop extrusion.
凝缩素在有丝分裂过程中使染色体浓缩,以促进其均等分离,但凝缩素与染色质结合并发挥作用的机制尚未完全阐明。在这里,我们表明,一般转录因子 TFIIH 复合物在转录沉默的卵提取物中连续需要建立和维持一个紧凑的染色体结构。抑制 TFIIH 复合物亚基 XPB 的 DNA 依赖性 ATP 酶活性可迅速且可逆地诱导染色体结构完全丧失,并阻止凝缩素 I 和 II 而不是拓扑异构酶 II 在染色质上的富集。此外,抑制 TFIIH 可防止在卵提取物中浓缩小鼠和 核,这表明 TFIIH 作用的一种进化保守机制。通过部分组蛋白耗竭降低核小体密度可恢复染色体结构和浓缩素的富集,而无需 TFIIH 活性。我们提出,TFIIH 复合物通过动态改变染色质环境来促进有丝分裂染色体浓缩,从而促进浓缩素的加载和浓缩素依赖性环挤出。