Molecular analysis of DNA polymerase eta gene in Japanese patients diagnosed as xeroderma pigmentosum variant type

被引:48
作者
Tanioka, Miki
Masaki, Taro
Ono, Ryusuke
Nagano, Tohru
Otoshi-Honda, Eriko
Matsumura, Yasuhiro
Takigawa, Masahiro
Inui, Hiroki
Miyachi, Yoshiki
Moriwaki, Shinichi
Nishigori, Chikako
机构
[1] Kobe Univ, Grad Sch Med, Div Dermatol, Dept Dermatol,Chuo Ku, Kobe, Hyogo 6500017, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Dermatol, Kyoto, Japan
[3] Hamamatsu Univ Sch Med, Dept Dermatol, Hamamatsu, Shizuoka 43131, Japan
[4] Natl Canc Inst, DNA Repair Sect, Basic Res Lab, Ctr Canc Res, Bethesda, MD USA
[5] Hamamatsu Univ Sch Med, Photon Med Res Ctr, Hamamatsu, Shizuoka 43131, Japan
关键词
D O I
10.1038/sj.jid.5700759
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
POLH mutations were identified in 16 Japanese patients, who were diagnosed, both clinically and at a cellular level, as being of the xeroderma pigmentosum variant type (XPV). While all the patients developed skin cancer with an average onset of the cancer at 45 years, in non-XP Japanese the onset was at over 70 years. All the cell strains from the patients were normal or slightly hypersensitive to UV and most of these showed enhanced UV sensitivity when the post-UV colony formation was performed in the presence of caffeine. Immunoprecipitation analysis with two kinds of anti-POLH protein antibodies revealed that cells from 13 patients did not show the 83 kDa POLH band and that cells from one patient had a faint 83 kDa band. All of these 14 cell strains, without a POLH band or with a weak POLH band, had mutations in the POLH gene. The IP analysis of the POLH protein revealed a very useful method for screening the patients suspected of XPV. Seven mutations in the POLH gene including three novel mutations were identified. Among the mutations detected, 11 alleles out of 28 (39%) were G490T mutations.
引用
收藏
页码:1745 / 1751
页数:7
相关论文
共 22 条
[1]   Molecular analysis of mutations in DNA polymerase η in xeroderma pigmentosum-variant patients [J].
Broughton, BC ;
Cordonnier, A ;
Kleijer, WJ ;
Jaspers, NGJ ;
Fawcett, H ;
Raams, A ;
Garritsen, VH ;
Stary, A ;
Avril, MF ;
Boudsocq, F ;
Masutani, C ;
Hanaoka, F ;
Fuchs, RP ;
Sarasin, A ;
Lehmann, AR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (02) :815-820
[2]  
CHAUNG TY, 1995, J AM ACAD DERMATOL, V33, P422
[3]  
Cleaver J.E., 1995, METABOLIC MOL BASIS, P4393
[4]   CAFFEINE TOXICITY IS INVERSELY RELATED TO DNA-REPAIR IN SIMIAN VIRUS-40-TRANSFORMED XERODERMA PIGMENTOSUM-CELLS IRRADIATED WITH ULTRAVIOLET-LIGHT [J].
CLEAVER, JE .
TERATOGENESIS CARCINOGENESIS AND MUTAGENESIS, 1989, 9 (03) :147-155
[5]   Molecular genetics of Xeroderma pigmentosum variant [J].
Gratchev, A ;
Strein, P ;
Utikal, J ;
Goerdt, S .
EXPERIMENTAL DERMATOLOGY, 2003, 12 (05) :529-536
[6]   XP43TO, previously classified as xeroderma pigmentosum group E, should be reclassified as xeroderma pigmentosum variant [J].
Itoh, T ;
Linn, S .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2001, 117 (06) :1672-1674
[7]   Xeroderma pigmentosum variant heterozygotes show reduced levels of recovery of replicative DNA synthesis in the presence of caffeine after ultraviolet irradiation [J].
Itoh, T ;
Linn, S ;
Kamide, R ;
Tokushige, H ;
Katori, N ;
Hosaka, Y ;
Yamaizumi, M .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2000, 115 (06) :981-985
[8]   hRAD30 mutations in the variant form of xeroderma pigmentosum [J].
Johnson, RE ;
Kondratick, CM ;
Prakash, S ;
Prakash, L .
SCIENCE, 1999, 285 (5425) :263-265
[9]   XERODERMA-PIGMENTOSUM - CUTANEOUS, OCULAR, AND NEUROLOGIC ABNORMALITIES IN 830 PUBLISHED CASES [J].
KRAEMER, KH ;
LEE, MM ;
SCOTTO, J .
ARCHIVES OF DERMATOLOGY, 1987, 123 (02) :241-250
[10]  
Laposa RR, 2003, CANCER RES, V63, P3909