High mobility group (HMG) proteins: Modulators of chromatin structure and DNA repair in mammalian cells

被引:73
|
作者
Reeves, Raymond [1 ]
机构
[1] Washington State Univ, Coll Vet Med, Sch Mol Biosci, Pullman, WA 99164 USA
关键词
Nucleotide excision repair (NER); Base excision repair (BER); Double-strand break repair (DSBR); Mismatch repair (MMR); Chromatin remodeling; HMGA; HMGB; HMGN; BASE EXCISION-REPAIR; DOUBLE-STRAND BREAKS; IN-VIVO MODULATION; V(D)J RECOMBINATION; CHROMOSOMAL-PROTEINS; HISTONE H1; POSTTRANSLATIONAL MODIFICATIONS; MOLECULAR-MECHANISMS; GENE-EXPRESSION; DAMAGE RESPONSE;
D O I
10.1016/j.dnarep.2015.09.015
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
It has been almost a decade since the last review appeared comparing and contrasting the influences that the different families of High Mobility Group proteins (HMGA, HMGB and HMGN) have on the various DNA repair pathways in mammalian cells. During that time considerable progress has been made in our understanding of how these non-histone proteins modulate the efficiency of DNA repair by all of the major cellular pathways: nucleotide excision repair, base excision repair, double-stand break repair and mismatch repair. Although there are often similar and over-lapping biological activities shared by all HMG proteins, members of each of the different families appear to have a somewhat 'individualistic' impact on various DNA repair pathways. This review will focus on what is currently known about the roles that different HMG proteins play in DNA repair processes and discuss possible future research areas in this rapidly evolving field. (c) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:122 / 136
页数:15
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