Sun Luyang, Yu Ruofan, Dang Weiwei
Huffington Center on Aging, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Genes (Basel). 2018 Apr 16;9(4):211. doi: 10.3390/genes9040211.
Chromatin 3D structure is highly dynamic and associated with many biological processes, such as cell cycle progression, cellular differentiation, cell fate reprogramming, cancer development, cellular senescence, and aging. Recently, by using chromosome conformation capture technologies, tremendous findings have been reported about the dynamics of genome architecture, their associated proteins, and the underlying mechanisms involved in regulating chromatin spatial organization and gene expression. Cellular senescence and aging, which involve multiple cellular and molecular functional declines, also undergo significant chromatin structural changes, including alternations of heterochromatin and disruption of higher-order chromatin structure. In this review, we summarize recent findings related to genome architecture, factors regulating chromatin spatial organization, and how they change during cellular senescence and aging.
染色质三维结构高度动态,并与许多生物学过程相关,如细胞周期进程、细胞分化、细胞命运重编程、癌症发展、细胞衰老和老化。最近,通过使用染色体构象捕获技术,已报道了关于基因组结构动态、其相关蛋白质以及调控染色质空间组织和基因表达的潜在机制的大量发现。细胞衰老和老化涉及多种细胞和分子功能衰退,也会发生显著的染色质结构变化,包括异染色质的改变和高阶染色质结构的破坏。在本综述中,我们总结了与基因组结构、调控染色质空间组织的因素以及它们在细胞衰老和老化过程中如何变化相关的最新发现。