The Fanconi anaemia pathway: newyplayers and new functions

被引:525
作者
Ceccaldi, Raphael
Sarangi, Prabha
D'Andrea, Alan D. [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Radiat Oncol, Boston, MA 02215 USA
基金
美国国家卫生研究院;
关键词
CROSS-LINK REPAIR; DOUBLE-STRAND BREAK; REPLICATION FORK RECOVERY; COMPLEMENTATION GROUP-M; DNA-POLYMERASE-ZETA; BONE-MARROW FAILURE; HOMOLOGOUS-RECOMBINATION; GENOME STABILITY; FANCD2; MONOUBIQUITINATION; XERODERMA-PIGMENTOSUM;
D O I
10.1038/nrm.2016.48
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Fanconi anaemia pathway repairs DNA interstrand crosslinks (ICLs) in the genome. Our understanding of this complex pathway is still evolving, as new components continue to be identified and new biochemical systems are used to elucidate the molecular steps of repair. The Fanconi anaemia pathway uses components of other known DNA repair processes to achieve proper repair of ICLs. Moreover, Fanconi anaemia proteins have functions in genome maintenance beyond their canonical roles of repairing ICLs. Such functions include the stabilization of replication forks and the regulation of cytokinesis. Thus, Fanconi anaemia proteins are emerging as master regulators of genomic integrity that coordinate several repair processes. Here, we summarize our current understanding of the functions of the Fanconi anaemia pathway in ICL repair, together with an overview of its connections with other repair pathways and its emerging roles in genome maintenance.
引用
收藏
页码:337 / 349
页数:13
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