Giles Katherine A, Taberlay Phillippa C, Cesare Anthony J, Jones Mathew J K
Children's Medical Research Institute, University of Sydney, Westmead, NSW, Australia.
Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia.
Front Cell Dev Biol. 2025 Feb 27;13:1548946. doi: 10.3389/fcell.2025.1548946. eCollection 2025.
Large eukaryotic genomes are packaged into the restricted area of the nucleus to protect the genetic code and provide a dedicated environment to read, copy and repair DNA. The physical organisation of the genome into chromatin loops and self-interacting domains provides the basic structural units of genome architecture. These structural arrangements are complex, multi-layered, and highly dynamic and influence how different regions of the genome interact. The role of chromatin structures during transcription via enhancer-promoter interactions is well established. Less understood is how nuclear architecture influences the plethora of chromatin transactions during DNA replication and repair. In this review, we discuss how genome architecture is regulated during the cell cycle to influence the positioning of replication origins and the coordination of DNA double strand break repair. The role of genome architecture in these cellular processes highlights its critical involvement in preserving genome integrity and cancer prevention.
大型真核生物基因组被包装在细胞核的有限区域内,以保护遗传密码,并提供一个专门的环境来读取、复制和修复DNA。基因组在染色质环和自我相互作用结构域中的物理组织提供了基因组结构的基本结构单元。这些结构排列复杂、多层且高度动态,并影响基因组不同区域的相互作用方式。染色质结构在通过增强子-启动子相互作用进行转录过程中的作用已得到充分证实。而对于核结构如何影响DNA复制和修复过程中大量的染色质事务,人们了解较少。在这篇综述中,我们讨论了基因组结构在细胞周期中是如何被调控的,以影响复制起点的定位和DNA双链断裂修复的协调。基因组结构在这些细胞过程中的作用凸显了其在维护基因组完整性和预防癌症方面的关键参与。