Distinct roles of RECQ1 in the maintenance of genomic stability

被引:32
作者
Wu, Yuliang [1 ]
Brosh, Robert M., Jr. [1 ]
机构
[1] NIA, Lab Mol Gerontol, NIH, Biomed Res Ctr, Baltimore, MD 21224 USA
关键词
RECQ1 (RECQL); RecQ; Helicase; Genomic stability; DNA repair; BLOOMS-SYNDROME HELICASE; REPLICATION PROTEIN-A; STRAND-ANNEALING ACTIVITIES; HOLLIDAY JUNCTION DISSOLVASOME; ROTHMUND-THOMSON-SYNDROME; TOPOISOMERASE-III-ALPHA; WERNER-SYNDROME PROTEIN; DNA HELICASE; HOMOLOGOUS RECOMBINATION; NEUROSPORA-CRASSA;
D O I
10.1016/j.dnarep.2009.12.010
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Five human RecQ helicases (WRN, BLM, RECQ4, RECQ5, RECQ1) exist in humans. Of these, three are genetically linked to diseases of premature aging and/or cancer. Neither RECQ1 nor RECQ5 has yet been implicated in a human disease. However, cellular studies and genetic analyses of model organisms indicate that RECQ1 (and RECQ5) play an important role in the maintenance of genomic stability. Biochemical studies of purified RECQ1 protein demonstrate that the enzyme catalyzes DNA unwinding and strand annealing, and these activities are likely to be important for its role in DNA repair. RECQ1 also physically and functionally interacts with proteins involved in genetic recombination. In this review, we will summarize our current knowledge of RECQ1 roles in cellular nucleic acid metabolism and propose avenues of investigation for future studies. Published by Elsevier B.V.
引用
收藏
页码:315 / 324
页数:10
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