Institute of Molecular Physiology, Shenzhen Bay Laboratory, Shenzhen, Guangdong, China.
Division of Hematology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA; Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Curr Opin Genet Dev. 2023 Jun;80:102036. doi: 10.1016/j.gde.2023.102036. Epub 2023 Apr 24.
All measurable features of higher-order chromosomal architecture undergo drastic reorganization as cells enter and exit mitosis. During mitosis, gene transcription is temporarily halted, the nuclear envelope is dismantled, and chromosomes undergo condensation. At this time, chromatin compartments, topologically associating domains (TADs), and loops that connect enhancers with promoters as well as CTCF/cohesin loops are dissolved. Upon G1 entry, genome organization is rebuilt in the daughter nuclei to resemble that of the mother nucleus. We survey recent studies that traced these features in relation to gene expression during the mitosis-to-G1-phase transition at high temporal resolution. Dissection of fluctuating architectural features informed the hierarchical relationships of chromosomal organization, the mechanisms by which they are formed, and their mutual (in-) dependence. These studies highlight the importance of considering the cell cycle dynamics for studies of chromosomal organization.
在细胞进入有丝分裂和退出有丝分裂的过程中,高级染色体结构的所有可测量特征都会发生剧烈的重组。在有丝分裂过程中,基因转录暂时停止,核膜解体,染色体发生浓缩。此时,染色质隔室、拓扑关联域 (TAD) 以及连接增强子与启动子的环以及 CTCF/黏合环都会溶解。进入 G1 期后,基因组组织在子核中重建,以类似于母核的方式。我们调查了最近的研究,这些研究在高时间分辨率下追踪了有丝分裂到 G1 期转变过程中与基因表达相关的这些特征。对波动的结构特征的剖析揭示了染色体组织的层次关系、它们形成的机制以及它们的相互(不)依赖性。这些研究强调了在研究染色体组织时考虑细胞周期动态的重要性。