DNA strand breaks at centromeres: Friend or foe?

被引:2
|
作者
Graham, Emily [1 ]
Esashi, Fumiko [1 ]
机构
[1] Univ Oxford, Sir William Dunn Sch Pathol, Oxford, England
基金
英国医学研究理事会;
关键词
Centromeres; DNA Damage; DNA Repair; Cell Cycle; Quiescence; ALPHA-SATELLITE DNA; CENP-A NUCLEOSOMES; TOPOISOMERASE-II ALPHA; CELL-CYCLE; R-LOOPS; MITOTIC RECOMBINATION; HISTONE H3; HOMOLOGOUS-RECOMBINATION; CHROMOSOME SEGREGATION; GENOMIC INSTABILITY;
D O I
10.1016/j.semcdb.2023.10.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Centromeres are large structural regions in the genomic DNA, which are essential for accurately transmitting a complete set of chromosomes to daughter cells during cell division. In humans, centromeres consist of highly repetitive alpha-satellite DNA sequences and unique epigenetic components, forming large proteinaceous structures required for chromosome segregation. Despite their biological importance, there is a growing body of evidence for centromere breakage across the cell cycle, including periods of quiescence. In this review, we provide an up-to-date examination of the distinct centromere environments at different stages of the cell cycle, highlighting their plausible contribution to centromere breakage. Additionally, we explore the implications of these breaks on centromere function, both in terms of negative consequences and potential positive effects.
引用
收藏
页码:141 / 151
页数:11
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