Rising from the RecQ-age: the role of human RecQ helicases in genome maintenance

被引:199
作者
Bohr, Vilhelm A. [1 ]
机构
[1] NIA, Lab Mol Gerontol, NIH, Baltimore, MD 21224 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.tibs.2008.09.003
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 RecQ helicases are guardians of the genome. Members of this conserved family of proteins have a key role in protecting and stabilizing the genome against deleterious changes. Deficiencies in RecQ helicases can lead to high levels of genomic instability and, in humans, to premature aging and increased susceptibility to cancer. Their diverse roles in DNA metabolism, which include a role in telomere maintenance, reflect interactions with multiple cellular proteins, some of which are multifunctional and also have very diverse functions. The results of in vitro cellular and biochemical studies have been complimented by recent in vivo studies using genetically modified mouse strains. Together, these approaches are helping to unravel the mechanism(s) of action and biological functions of the RecQ helicases.
引用
收藏
页码:609 / 620
页数:12
相关论文
共 99 条
[1]   Epigenetic inactivation of the premature aging Werner syndrome gene in human cancer [J].
Agrelo, Ruben ;
Cheng, Wen-Hsing ;
Setien, Fernando ;
Ropero, Santiago ;
Espada, Jesus ;
Fraga, Mario F. ;
Herranz, Michel ;
Paz, Maria F. ;
Sanchez-Cespedes, Montserrat ;
Artiga, Maria Jesus ;
Guerrero, David ;
Castells, Antoni ;
von Kobbe, Cayetano ;
Bohr, Vilheirn A. ;
Esteller, Manel .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (23) :8822-8827
[2]   Regulation of WRN helicase activity in human base excision repair [J].
Ahn, B ;
Harrigan, JA ;
Indig, FE ;
Wilson, DM ;
Bohr, VA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (51) :53465-53474
[3]   A RECQ5-RNA polymerase II association identified by targeted proteomic analysis of human chromatin [J].
Aygun, Ozan ;
Svejstrup, Jesper ;
Liu, Yilun .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (25) :8580-8584
[4]   Analysis of the DNA unwinding activity of RecQ family helicases [J].
Bachrati, Csanad Z. ;
Hickson, Ian D. .
DNA REPAIR, PT B, 2006, 409 :86-100
[5]   The Werner syndrome protein is involved in RNA polymerase II transcription [J].
Balajee, AS ;
Machwe, A ;
May, A ;
Gray, MD ;
Oshima, J ;
Martin, GM ;
Nehlin, JO ;
Brosh, R ;
Orren, DK ;
Bohr, VA .
MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (08) :2655-2668
[6]   WRN interacts physically and functionally with the recombination mediator protein RAD52 [J].
Baynton, K ;
Otterlei, M ;
Bjorås, M ;
von Kobbe, C ;
Bohr, VA ;
Seeberg, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (38) :36476-36486
[7]   DNA damage-induced translocation of the Werner helicase is regulated by acetylation [J].
Blander, G ;
Zalle, N ;
Daniely, Y ;
Taplick, J ;
Gray, MD ;
Oren, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (52) :50934-50940
[8]   The Werner syndrome protein confers resistance to the DNA lesions N3-methyladenine and O6-methylguanine:: implications for WRN function [J].
Blank, A ;
Bobola, MS ;
Gold, B ;
Varadarajan, S ;
Kolstoe, DD ;
Meade, EH ;
Rabinovitch, PS ;
Loeb, LA ;
Silber, JR .
DNA REPAIR, 2004, 3 (06) :629-638
[9]   Functional interaction between the Bloom's syndrome helicase and the RAD51 paralog, RAD51L3 (RAD51D) [J].
Braybrooke, JP ;
Li, JL ;
Wu, L ;
Caple, F ;
Benson, FE ;
Hickson, ID .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (48) :48357-48366
[10]   Replication protein A physically interacts with the Bloom's syndrome protein and stimulates its helicase activity [J].
Brosh, RM ;
Li, JL ;
Kenny, MK ;
Karow, JK ;
Cooper, MP ;
Kureekattil, RP ;
Hickson, ID ;
Bohr, VA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (31) :23500-23508