生物
DNA复制
染色体脆性位点
基因组不稳定性
有丝分裂
遗传学
复制前复合体
变色
染色体分离
端粒
染色体不稳定性
细胞生物学
芽殖酵母
染色体
DNA
原点识别复合体
染色体复制控制
真核细胞DNA复制
DNA再复制
DNA损伤
许可因素
基因
酿酒酵母
作者
Esther A. Epum,James E. Haber
标识
DOI:10.1016/j.tcb.2021.07.005
摘要
Failure to complete DNA replication is one of the major sources of genome instability leading to aneuploidy, chromosome breakage, and chromosome rearrangements that are associated with human cancer. One of the surprising revelations of the past decade is that the completion of replication at so-called common fragile sites (CFS) occurs very late in the cell cycle – at mitosis – through a process termed MiDAS (mitotic DNA synthesis). MiDAS is strongly related to another cancer-promoting phenomenon: the activation of alternative lengthening of telomeres (ALT). Our understanding of the mechanisms of ALT and MiDAS in mammalian cells has drawn heavily from recent advances in the study of break-induced replication (BIR), especially in budding yeast. We provide new insights into the BIR, MiDAS, and ALT pathways and their shared similarities.
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