Literature DB >> 9256465

The human XRCC9 gene corrects chromosomal instability and mutagen sensitivities in CHO UV40 cells.

N Liu1, J E Lamerdin, J D Tucker, Z Q Zhou, C A Walter, J S Albala, D B Busch, L H Thompson.   

Abstract

The Chinese hamster ovary (CHO) mutant UV40 cell line is hypersensitive to UV and ionizing radiation, simple alkylating agents, and DNA cross-linking agents. The mutant cells also have a high level of spontaneous chromosomal aberrations and 3-fold elevated sister chromatid exchange. We cloned and sequenced a human cDNA, designated XRCC9, that partially corrected the hypersensitivity of UV40 to mitomycin C, cisplatin, ethyl methanesulfonate, UV, and gamma-radiation. The spontaneous chromosomal aberrations in XRCC9 cDNA transformants were almost fully corrected whereas sister chromatid exchanges were unchanged. The XRCC9 genomic sequence was cloned and mapped to chromosome 9p13. The translated XRCC9 sequence of 622 amino acids has no similarity with known proteins. The 2.5-kb XRCC9 mRNA seen in the parental cells was undetectable in UV40 cells. The mRNA levels in testis were up to 10-fold higher compared with other human tissues and up to 100-fold higher compared with other baboon tissues. XRCC9 is a candidate tumor suppressor gene that might operate in a postreplication repair or a cell cycle checkpoint function.

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Year:  1997        PMID: 9256465      PMCID: PMC23130          DOI: 10.1073/pnas.94.17.9232

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  57 in total

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Journal:  Mutat Res       Date:  1993-01       Impact factor: 2.433

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4.  Selective extraction of polyoma DNA from infected mouse cell cultures.

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Journal:  J Mol Biol       Date:  1967-06-14       Impact factor: 5.469

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Journal:  Cytogenet Cell Genet       Date:  1988

6.  Molecular cloning of the human XRCC1 gene, which corrects defective DNA strand break repair and sister chromatid exchange.

Authors:  L H Thompson; K W Brookman; N J Jones; S A Allen; A V Carrano
Journal:  Mol Cell Biol       Date:  1990-12       Impact factor: 4.272

7.  A CHO mutant, UV40, that is sensitive to diverse mutagens and represents a new complementation group of mitomycin C sensitivity.

Authors:  D B Busch; M Z Zdzienicka; A T Natarajan; N J Jones; W J Overkamp; A Collins; D L Mitchell; M Stefanini; E Botta; R B Albert; N Liu; D A White; A J van Gool; L H Thompson
Journal:  Mutat Res       Date:  1996-08-08       Impact factor: 2.433

Review 8.  Menage à trois: double strand break repair, V(D)J recombination and DNA-PK.

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Journal:  Bioessays       Date:  1995-11       Impact factor: 4.345

9.  Xeroderma pigmentosum cells with normal levels of excision repair have a defect in DNA synthesis after UV-irradiation.

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Journal:  Proc Natl Acad Sci U S A       Date:  1975-01       Impact factor: 11.205

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Authors:  J R Lo Ten Foe; M A Rooimans; L Bosnoyan-Collins; N Alon; M Wijker; L Parker; J Lightfoot; M Carreau; D F Callen; A Savoia; N C Cheng; C G van Berkel; M H Strunk; J J Gille; G Pals; F A Kruyt; J C Pronk; F Arwert; M Buchwald; H Joenje
Journal:  Nat Genet       Date:  1996-11       Impact factor: 38.330

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  11 in total

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5.  Fanconi anemia proteins FANCA, FANCC, and FANCG/XRCC9 interact in a functional nuclear complex.

Authors:  I Garcia-Higuera; Y Kuang; D Näf; J Wasik; A D D'Andrea
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Review 6.  Molecular pathogenesis of fanconi anemia.

Authors:  Toshiyasu Taniguchi; Alan D Dandrea
Journal:  Int J Hematol       Date:  2002-02       Impact factor: 2.490

7.  Fanconi anemia FANCG protein in mitigating radiation- and enzyme-induced DNA double-strand breaks by homologous recombination in vertebrate cells.

Authors:  Kazuhiko Yamamoto; Masamichi Ishiai; Nobuko Matsushita; Hiroshi Arakawa; Jane E Lamerdin; Jean-Marie Buerstedde; Mitsune Tanimoto; Mine Harada; Larry H Thompson; Minoru Takata
Journal:  Mol Cell Biol       Date:  2003-08       Impact factor: 4.272

8.  Impairment of APE1 function enhances cellular sensitivity to clinically relevant alkylators and antimetabolites.

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9.  FANCG is phosphorylated at serines 383 and 387 during mitosis.

Authors:  Jun Mi; Fengyu Qiao; James B Wilson; Anthony A High; Melanie J Schroeder; Peter T Stukenberg; Amy Moss; Jeffrey Shabanowitz; Donald F Hunt; Nigel J Jones; Gary M Kupfer
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10.  Gene expression studies in multiple sclerosis.

Authors:  Lotti Tajouri; Francesca Fernandez; Lyn R Griffiths
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