Oligonucleotide/oligosaccharide-binding fold proteins: a growing family of genome guardians

被引:141
作者
Flynn, Rachel Litman [2 ]
Zou, Lee [1 ,2 ]
机构
[1] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Ctr Canc, Charlestown, MA USA
关键词
OB fold; DNA damage; checkpoint; telomere; DNA repair; SINGLE-STRANDED-DNA; TOPOISOMERASE-III-ALPHA; OB-FOLD; DAMAGE RESPONSE; HUMAN POT1; TELOMERASE PROCESSIVITY; ESSENTIAL COMPONENT; PROTECTS TELOMERES; ALTERNATIVE FORM; BASIC CLEFT;
D O I
10.3109/10409238.2010.488216
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
The maintenance of genomic stability relies on the coordinated action of a number of cellular processes, including activation of the DNA-damage checkpoint, DNA replication, DNA repair, and telomere homeostasis. Many proteins involved in these cellular processes use different types of functional modules to regulate and execute their functions. Recent studies have revealed that many DNA-damage checkpoint and DNA repair proteins in human cells possess the oligonucleotide/oligosaccharide-binding (OB) fold domains, which are known to bind single-stranded DNA in both prokaryotes and eukaryotes. Furthermore, during the DNA damage response, the OB folds of the human checkpoint and DNA repair proteins play critical roles in DNA binding, protein complex assembly, and regulating protein-protein interactions. These findings suggest that the OB fold is an evolutionarily conserved functional module that is widely used by genome guardians. In this review, we will highlight the functions of several well-characterized or newly discovered eukaryotic OB-fold proteins in the DNA damage response.
引用
收藏
页码:266 / 275
页数:10
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