RDM1, a novel RNA recognition motif (RRM)-containing protein involved in the cell response to cisplatin in vertebrates

被引:30
作者
Hamimes, S
Arakawa, H
Stasiak, AZ
Kierzek, AM
Hirano, S
Yang, YG
Takata, M
Stasiak, A
Buerstedde, JM
Van Dyck, E
机构
[1] Int Agcy Res Canc, F-69732 Lyon, France
[2] GSF, Inst Mol Radiobiol, D-85764 Neuherberg, Germany
[3] Univ Lausanne, Lab Anal Ultrastruct, CH-1015 Lausanne, Switzerland
[4] Univ Surrey, SBMS, Guildford GU2 7XH, Surrey, England
[5] Kawasaki Med Sch, Kurashiki, Okayama 7010192, Japan
[6] Polish Acad Sci, Inst Biochem & Biophys, PL-02106 Warsaw, Poland
关键词
D O I
10.1074/jbc.M412874200
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
A variety of cellular proteins has the ability to recognize DNA lesions induced by the anti-cancer drug cisplatin, with diverse consequences on their repair and on the therapeutic effectiveness of this drug. We report a novel gene involved in the cell response to cisplatin in vertebrates. The RDM1 gene ( for (R) under barA (D) under bar 52 (M) under bar otif 1) was identified while searching databases for sequences showing similarities to RAD52, a protein involved in homologous recombination and DNA double-strand break repair. Ablation of RDM1 in the chicken B cell line DT40 led to a more than 3-fold increase in sensitivity to cisplatin. However, RDM1(-/-) cells were not hypersensitive to DNA damages caused by ionizing radiation, UV irradiation, or the alkylating agent methylmethane sulfonate. The RDM1 protein displays a nucleic acid binding domain of the RNA recognition motif (RRM) type. By using gel-shift assays and electron microscopy, we show that purified, recombinant chicken RDM1 protein interacts with single-stranded DNA as well as double-stranded DNA, on which it assembles filament-like structures. Notably, RDM1 recognizes DNA distortions induced by cisplatin-DNA adducts in vitro. Finally, human RDM1 transcripts are abundant in the testis, suggesting a possible role during spermatogenesis.
引用
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页码:9225 / 9235
页数:11
相关论文
共 80 条
[61]  
SOGO JM, 1987, ELECTRON MICROS, P61
[62]   The human Rad52 protein exists as a heptameric ring [J].
Stasiak, AZ ;
Larquet, E ;
Stasiak, A ;
Müller, S ;
Engel, A ;
Van Dyck, E ;
West, SC ;
Egelman, EH .
CURRENT BIOLOGY, 2000, 10 (06) :337-340
[63]   Rad51 recombinase and recombination mediators [J].
Sung, P ;
Krejci, L ;
Van Komen, S ;
Sehorn, MG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (44) :42729-42732
[64]   Homologous recombination and non-homologous end-joining pathways of DNA double-strand break repair have overlapping roles in the maintenance of chromosomal integrity in vertebrate cells [J].
Takata, M ;
Sasaki, MS ;
Sonoda, E ;
Morrison, C ;
Hashimoto, M ;
Utsumi, H ;
Yamaguchi-Iwai, Y ;
Shinohara, A ;
Takeda, S .
EMBO JOURNAL, 1998, 17 (18) :5497-5508
[65]   Critical DNA damage recognition functions of XPC-hHR23B and XPA-RPA in nucleotide excision repair [J].
Thoma, BS ;
Vasquez, KM .
MOLECULAR CARCINOGENESIS, 2003, 38 (01) :1-13
[66]   The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools [J].
Thompson, JD ;
Gibson, TJ ;
Plewniak, F ;
Jeanmougin, F ;
Higgins, DG .
NUCLEIC ACIDS RESEARCH, 1997, 25 (24) :4876-4882
[67]   ATP-dependent chromatin remodeling facilitates nucleotide excision repair of UV-induced DNA lesions in synthetic dinucleosomes [J].
Ura, K ;
Araki, M ;
Saeki, H ;
Masutani, C ;
Ito, T ;
Iwai, S ;
Mizukoshi, T ;
Kaneda, Y ;
Hanaoka, F .
EMBO JOURNAL, 2001, 20 (08) :2004-2014
[68]  
van den Bosch M, 2002, BIOL CHEM, V383, P873
[69]   Visualisation of human Rad52 protein and its complexes with hRad51 and DNA [J].
Van Dyck, E ;
Hajibagheri, NMA ;
Stasiak, A ;
West, SC .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 284 (04) :1027-1038
[70]   Visualization of recombination intermediates produced by RAD52-mediated single-strand annealing [J].
Van Dyck, E ;
Stasiak, AZ ;
Stasiak, A ;
West, SC .
EMBO REPORTS, 2001, 2 (10) :905-909