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GM04429 Fibroblast

Description:

XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA
XPA, DNA DAMAGE RECOGNITION AND REPAIR FACTOR; XPA

Affected:

Yes

Sex:

Female

Age:

7 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Class Repair Defective and Chromosomal Instability Syndromes
Cell Type Fibroblast
Transformant Simian Virus 40
Race White
Family Member 1
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Multiple skin cancers; acute sun sensitivity; progressive neurological degeneration; T-antigen positive; the donor subject is a compound heterozygote for two mutations in the XPA gene: one allele carries a G-to-C substitution at nucleotide 555 (555G>C) in exon 4 with results in a missplice; the second allele carries a G-to-T transversion in intron 3 which abolishes the canonical 3-prime splice site and results in a missplice; less than 2% of normal UV induced unscheduled DNA synthesis in fibroblasts; XP12BE; SV40 transformed; passage 7 at CCR; see GM02250 (lymphoblast) and GM05509 (fibroblast).

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis and by Chromosome Analysis
 
Gene XPA
Chromosomal Location 9q22.3-q31
Allelic Variant 1 missplice; XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A
Identified Mutation 555G>C
 
Gene XPA
Chromosomal Location 9q22.3-q31
Allelic Variant 2 missplice; XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A
Identified Mutation G>T transversion in intron 3

Phenotypic Data

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Remarks Multiple skin cancers; acute sun sensitivity; progressive neurological degeneration; T-antigen positive; the donor subject is a compound heterozygote for two mutations in the XPA gene: one allele carries a G-to-C substitution at nucleotide 555 (555G>C) in exon 4 with results in a missplice; the second allele carries a G-to-T transversion in intron 3 which abolishes the canonical 3-prime splice site and results in a missplice; less than 2% of normal UV induced unscheduled DNA synthesis in fibroblasts; XP12BE; SV40 transformed; passage 7 at CCR; see GM02250 (lymphoblast) and GM05509 (fibroblast).

Publications

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Leggett CS, Doll MA, States JC, Hein DW, Acetylation of putative arylamine and alkylaniline carcinogens in immortalized human fibroblasts transfected with rapid and slow acetylator N-acetyltransferase 2 haplotypes Archives of toxicology: 2020
PubMed ID: 33136180
 
Yoon JH, Basu D, Sellamuthu K, Johnson RE, Prakash S, Prakash L, A novel role of DNA polymerase ? in translesion synthesis in conjunction with DNA polymerase ? Life science alliance4: 2020
PubMed ID: 33514655
 
Sarker AH, Trego KS, Zhang W, Jacob P, Snijders A, Mao JH, Schick SF, Cooper PK, Hang B, Thirdhand Smoke Exposure Causes Replication Stress and Impaired Transcription in Human Lung Cells Environmental and molecular mutagenesis4: 2019
PubMed ID: 32267018
 
Shafirovich V, Kropachev K, Kolbanovskiy M, Geacintov NE, Excision of Oxidatively Generated Guanine Lesions by Competing Base and Nucleotide Excision Repair Mechanisms in Human Cells Chemical research in toxicology4: 2019
PubMed ID: 30688445
 
Ræder SB, Nepal A, Bjørås KØ, Seelinger M, Kolve RS, Nedal A, Müller R, Otterlei M, APIM-Mediated REV3L?PCNA Interaction Important for Error Free TLS Over UV-Induced DNA Lesions in Human Cells International journal of molecular sciences20: 2018
PubMed ID: 30597836
 
Yoon JH, McArthur MJ, Park J, Basu D, Wakamiya M, Prakash L, Prakash S, Error-Prone Replication through UV Lesions by DNA Polymerase ? Protects against Skin Cancers Cell176:1295-1309.e15 2018
PubMed ID: 30773314
 
Mazouzi A, Battistini F, Moser SC, Ferreira da Silva J, Wiedner M, Owusu M, Lardeau CH, Ringler A, Weil B, Neesen J, Orozco M, Kubicek S, Loizou JI, Repair of UV-Induced DNA Damage Independent of Nucleotide Excision Repair Is Masked by MUTYH Molecular cell68:797-807.e7 2017
PubMed ID: 29149600
 
Hu J, Choi JH, Gaddameedhi S, Kemp MG, Reardon JT, Sancar A, Nucleotide excision repair in human cells: fate of the excised oligonucleotide carrying DNA damage in vivo The Journal of biological chemistry288:20918-26 2013
PubMed ID: 23749995
 
Gilljam KM, Müller R, Liabakk NB, Otterlei M, Nucleotide excision repair is associated with the replisome and its efficiency depends on a direct interaction between XPA and PCNA PloS one7:e49199 2012
PubMed ID: 23152873
 
Fan W, Luo J, SIRT1 regulates UV-induced DNA repair through deacetylating XPA Molecular cell39:247-58 2009
PubMed ID: 20670893
 
Fan W, Luo J, RecQ4 facilitates UV-induced DNA damage repair through interaction with nucleotide excision repair factor XPA The Journal of biological chemistry39:247-58 2008
PubMed ID: 18693251
 
Wu X, Shell SM, Yang Z, Zou Y, Phosphorylation of nucleotide excision repair factor xeroderma pigmentosum group A by ataxia telangiectasia mutated and Rad3-related-dependent checkpoint pathway promotes cell survival in response to UV irradiation Cancer research66:2997-3005 2006
PubMed ID: 16540648
 
Kalish JM, Seidman MM, Weeks DL, Glazer PM, Triplex-induced recombination and repair in the pyrimidine motif. Nucleic Acids Res33(11):3492-502 2005
PubMed ID: 15961731
 
Gao H, Chen XB, McGowan CH, Mus81 endonuclease localizes to nucleoli and to regions of DNA damage in human S-phase cells. Mol Biol Cell14(12):4826-34 2003
PubMed ID: 14638871
 
Morelli C, Karayianni E, Magnanini C, Mungall AJ, Thorland E, Negrini M, Smith DI, Barbanti-Brodano G, Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors Oncogene21:7266-76 2002
PubMed ID: 12370818
 
Oakley GG, Loberg LI, Yao J, Risinger MA, Yunker RL, Zernik-Kobak M, Khanna KK, Lavin MF, Carty MP, Dixon K, UV-induced hyperphosphorylation of replication protein a depends on DNA replication and expression of ATM protein. Mol Biol Cell12(5):1199-213 2001
PubMed ID: 11359916
 
Prince PR, Ogburn CE, Moser MJ, Emond MJ, Martin GM, Monnat RJ Jr, Cell fusion corrects the 4-nitroquinoline 1-oxide sensitivity of Werner syndrome fibroblast cell lines. Hum Genet105:132-8 1999
PubMed ID: 10480367
 
Cordeiro-Stone M, Zaritskaya LS, Price LK, Kaufmann WK, Replication fork bypass of a pyrimidine dimer blocking leading strand DNA synthesis. J Biol Chem272:13945-13954 1997
PubMed ID: 9153257
 
Merk O, Speit G, Characterization of SV40-transformed xeroderma pigmentosum cell lines for their usability in HPRT mutation studies. Mutagenesis12(5):391-5 1997
PubMed ID: 9379920
 
Myrand SP, Topping RS, States JC, Stable transformation of xeroderma pigmentosum group A cells with an XPA minigene restores normal DNA repair and mutagenesis of UV-treated plasmids. Carcinogenesis17(9):1909-17 1996
PubMed ID: 8824513
 
States JC, Myrand SP, Splice site mutations in a xeroderma pigmentosum group A patient with delayed onset of neurological disease. Mutat Res363:171-7 1996
PubMed ID: 8765158
 
Wang G, Seidman MM, Glazer PM, Mutagenesis in mammalian cells induced by triple helix formation and transcription-coupled repair. Science271(5250):802-5 1996
PubMed ID: 8628995
 
Endo H, Schut HA, Snyderwine EG, Mutagenic specificity of 2-amino-3-methylimidazo[4,5-f]quinoline and 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine in the supF shuttle vector system. Cancer Res54(14):3745-51 1994
PubMed ID: 8033094
 
Meyn MS, High spontaneous intrachromosomal recombination rates in ataxia- telangiectasia. Science260:1327-30 1993
PubMed ID: 8493577
 
States JC, Quan T, Hines RN, Novak RF, Runge-Morris M, Expression of human cytochrome P450 1A1 in DNA repair deficient and proficient human fibroblasts stably transformed with an inducible expression vector. Carcinogenesis14:1643-9 1993
PubMed ID: 8353849
 
Levy DD, Groopman JD, Lim SE, Seidman MM, Kraemer KH, Sequence specificity of aflatoxin B1-induced mutations in a plasmid replicated in xeroderma pigmentosum and DNA repair proficient human cells. Cancer Res52:5668-73 1992
PubMed ID: 1394191
 
Luethy JD, Holbrook NJ, Activation of the gadd153 promoter by genotoxic agents: a rapid and specific response to DNA damage. Cancer Res52:5-10 1992
PubMed ID: 1727386
 
Ben-Ishai R, Scharf R, Sharon R, Kapten I, A human cellular sequence implicated in trk oncogene activation is DNA damage inducible. Proc Natl Acad Sci U S A87:6039-43 1990
PubMed ID: 1696715
 
Rinaldy A, Bellew T, Egli E, Lloyd RS, Increased UV resistance in xeroderma pigmentosum group A cells after transformation with a human genomic DNA clone. Proc Natl Acad Sci U S A87:6818-22 1990
PubMed ID: 2168562
 
Lattier DL, States JC, Hutton JJ, Wiginton DA, Cell type-specific transcriptional regulation of the human adenosine deaminase gene. Nucleic Acids Res17:1061-76 1989
PubMed ID: 2784203
 
Akeson AL, Wiginton DA, Dusing MR, States JC, Hutton JJ, Mutant human adenosine deaminase alleles and their expression by transfection into fibroblasts. J Biol Chem263:16291-6 1988
PubMed ID: 3182793
 
Protic M, Roilides E, Levine AS, Dixon K, Enhancement of DNA repair capacity of mammalian cells by carcinogen treatment. Somat Cell Mol Genet14:351-7 1988
PubMed ID: 3135602
 
Brash DE, Seetharam S, Kraemer KH, Seidman MM, Bredberg A, Photoproduct frequency is not the major determinant of UV base substitution hot spots or cold spots in human cells. Proc Natl Acad Sci U S A84:3782-6 1987
PubMed ID: 3473483
 
Seidman MM, Bredberg A, Seetharam S, Kraemer KH, Multiple point mutations in a shuttle vector propagated in human cells: evidence for an error-prone DNA polymerase activity. Proc Natl Acad Sci U S A84:4944-8 1987
PubMed ID: 3474635
 
Bredberg A, Kraemer KH, Seidman MM, Restricted ultraviolet mutational spectrum in a shuttle vector propagated in xeroderma pigmentosum cells. Proc Natl Acad Sci U S A83:8273-7 1986
PubMed ID: 3464953
 
Protic-Sabljic M, Kraemer KH, Host cell reactivation by human cells of DNA expression vectors damaged by ultraviolet radiation or by acid-heat treatment. Carcinogenesis7:1765-70 1986
PubMed ID: 3463438
 
Protic-Sabljic M, Kraemer KH, Reduced repair of non-dimer photoproducts in a gene transfected into xeroderma pigmentosum cells. Photochem Photobiol43:509-13 1986
PubMed ID: 3526363
 
Kuhnlein U, Comparison of apurinic DNA-binding protein from an ataxia telangiectasia and a HeLa cell line. Evidence for an altered processing of apurinic/apyrimidinic endonuclease. J Biol Chem260:14918-24 1985
PubMed ID: 2415510
 
Protic-Sabljic M, Kraemer KH, One pyrimidine dimer inactivates expression of a transfected gene in xeroderma pigmentosum cells. Proc Natl Acad Sci U S A82:6622-6 1985
PubMed ID: 2995975
 
Kuhnlein U, Tsang SS, Lokken O, Tong S, Twa D, Cell lines from xeroderma pigmentosum complementation group A lack a single-stranded-DNA-binding activity. Biosci Rep3:667-74 1983
PubMed ID: 6684957
 
Protic-Sabljic, Transfection of Xeroderma pigmentosum cells with cloned DNA (from Cellular Responses To DNA Damage, Alan R. Liss, Inc .) "Cellular Respon To DNA Damage"1983,pp647:667-74 1983
PubMed ID: 6684957
 
Lin PF, Slate DL, Lawyer FC, Ruddle FH, Assignment of the murine interferon sensitivity and cytoplasmic superoxide dismutase genes to chromosome 16. Science209:285-7 1980
PubMed ID: 6155698

External Links

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dbSNP dbSNP ID: 14160
Gene Cards XPA
Gene Ontology GO:0003684 damaged DNA binding
GO:0005515 protein binding
GO:0005634 nucleus
GO:0006289 nucleotide-excision repair
NCBI Gene Gene ID:7507
NCBI GTR 278700 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA
611153 XPA GENE; XPA
OMIM 278700 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA
611153 XPA GENE; XPA
Omim Description XERODERMA PIGMENTOSUM I; XP1
  XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA
  XP, GROUP A
  XPA COMPLEMENTING; XPAC
  XPA CORRECTING

Culture Protocols

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Split Ratio 1:5
Temperature 37 C
Percent CO2 5%
Medium Eagle's Minimum Essential Medium with Earle's salts and non-essential amino acids with 2mM L-glutamine or equivalent
Serum 10% fetal bovine serum Not inactivated
Substrate None specified
Subcultivation Method trypsin-EDTA
Supplement -
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International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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