Mouse WRN Helicase Domain Is Not Required for Spontaneous Homologous Recombination-Mediated DNA Deletion

被引:3
作者
Brown, Adam D. [1 ,2 ]
Claybon, Alison B. [1 ]
Bishop, Alexander J. R. [1 ,2 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Greehey Childrens Canc Res Inst, San Antonio, TX 78229 USA
[2] Univ Texas Hlth Sci Ctr San Antonio, Dept Cellular & Struct Biol, San Antonio, TX 78229 USA
基金
美国国家卫生研究院;
关键词
D O I
10.4061/2010/356917
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
Werner syndrome is a rare disorder that manifests as premature aging and age-related diseases. WRN is the gene mutated in WS, and is one of five human RecQ helicase family members. WS cells exhibit genomic instability and altered proliferation, and in vitro studies suggest that WRN has a role in suppressing homologous recombination. However, more recent studies propose that other RecQ helicases (including WRN) promote early events of homologous recombination. To study the role of WRN helicase on spontaneous homologous recombination, we obtained a mouse with a deleted WRN helicase domain and combined it with the in vivo pink-eyed unstable homologous recombination system. In this paper, we demonstrate that WRN helicase is not necessary for suppressing homologous recombination in vivo contrary to previous reports using a similar mouse model.
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页数:6
相关论文
共 43 条
[1]   DNA double-strand breaks associated with replication forks are predominantly repaired by homologous recombination involving an exchange mechanism in mammalian cells [J].
Arnaudeau, C ;
Lundin, C ;
Helleday, T .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 307 (05) :1235-1245
[2]   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
[3]   p21 controls patterning but not homologous recombination in RPE development [J].
Bishop, AJR ;
Kosaras, B ;
Hollander, MC ;
Fornace, A ;
Sidman, RL ;
Schiestl, RH .
DNA REPAIR, 2006, 5 (01) :111-120
[4]  
Bishop AJR, 2003, CANCER RES, V63, P5335
[5]   Susceptibility of proliferating cells to benzo[a]pyrene-induced homologous recombination in mice [J].
Bishop, AJR ;
Kosaras, B ;
Carls, N ;
Sidman, RL ;
Schiestl, RH .
CARCINOGENESIS, 2001, 22 (04) :641-649
[6]   Benzo(a)pyrene and X-rays induce reversions of the pink-eyed unstable mutation in the retinal pigment epithelium of mice [J].
Bishop, AJR ;
Kosaras, B ;
Sidman, RL ;
Schiestl, RH .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2000, 457 (1-2) :31-40
[7]   GROWTH AND DEVELOPMENT OF THE MOUSE RETINAL-PIGMENT EPITHELIUM .1. CELL AND TISSUE MORPHOMETRICS AND TOPOGRAPHY OF MITOTIC-ACTIVITY [J].
BODENSTEIN, L ;
SIDMAN, RL .
DEVELOPMENTAL BIOLOGY, 1987, 121 (01) :192-204
[8]   Functional and physical interaction between WRN helicase and human replication protein A [J].
Brosh, RM ;
Orren, DK ;
Nehlin, JO ;
Ravn, PH ;
Kenny, MK ;
Machwe, A ;
Bohr, VA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (26) :18341-18350
[9]   HOMOLOGOUS RECOMBINATION IS ELEVATED IN SOME WERNER-LIKE SYNDROMES BUT NOT DURING NORMAL INVITRO OR INVIVO SENESCENCE OF MAMMALIAN-CELLS [J].
CHENG, RZ ;
MURANO, S ;
KURZ, B ;
REIS, RJS .
MUTATION RESEARCH, 1990, 237 (5-6) :259-269
[10]  
Claybon A. B., 2010, NUCLEIC ACIDS RES, P1