Around and beyond 53BP1 Nuclear Bodies

被引:26
|
作者
Fernandez-Vidal, Anne [1 ]
Vignard, Julien [1 ]
Mirey, Gladys [1 ]
机构
[1] Univ Toulouse, INP Purpan, ENVT, Toxalim Res Ctr Food Toxicol,INRA,UPS, F-31027 Toulouse, France
关键词
53BP1; nuclear bodies; DNA damage; replication stress; common fragile sites; genetic instability; cancer; DOUBLE-STRAND BREAKS; DNA-POLYMERASE KAPPA; COMMON FRAGILE SITES; PROLIFERATION-QUIESCENCE DECISION; ENDOGENOUS REPLICATION STRESS; GENOMIC INSTABILITY; HOMOLOGOUS RECOMBINATION; CELLULAR SENESCENCE; DAMAGE RESPONSE; REPAIR PATHWAY;
D O I
10.3390/ijms18122611
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Within the nucleus, sub-nuclear domains define territories where specific functions occur. Nuclear bodies (NBs) are dynamic structures that concentrate nuclear factors and that can be observed microscopically. Recently, NBs containing the p53 binding protein 1 (53BP1), a key component of the DNA damage response, were defined. Interestingly, 53BP1 NBs are visualized during G1 phase, in daughter cells, while DNA damage was generated in mother cells and not properly processed. Unlike most NBs involved in transcriptional processes, replication has proven to be key for 53BP1 NBs, with replication stress leading to the formation of these large chromatin domains in daughter cells. In this review, we expose the composition and organization of 53BP1 NBs and focus on recent findings regarding their regulation and dynamics. We then concentrate on the importance of the replication stress, examine the relation of 53BP1 NBs with DNA damage and discuss their dysfunction.
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页数:20
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