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Cellosaurus XP12RO (CVCL_VP50)

[Text version]
Cell line name XP12RO
Synonyms XP12RO-SV40; XP12RO(SV40); XP12ROSV
Accession CVCL_VP50
Resource Identification Initiative To cite this cell line use: XP12RO (RRID:CVCL_VP50)
Comments Population: Palestinian.
Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40).
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
Disease Xeroderma pigmentosum, complementation group A (NCIt: C3965)
Xeroderma pigmentosum (ORDO: Orphanet_910)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_VP51 (XP129)CVCL_VP52 (XP12ROB4)
Sex of cell Male
Age at sampling 12Y
Category Transformed cell line
Publications

PubMed=4436596; DOI=10.1111/1523-1747.ep12676556
Vazken Movses Der Kaloustian, Elizabeth A. de Weerd-Kastelein, Wim J. Kleijer, Wilma Keijzer, Dirk Bootsma;
The genetic defect in the de Sanctis-Cacchione syndrome.
J. Invest. Dermatol. 63:392-396(1974)

PubMed=6256643; DOI=10.1038/288724a0
Rufus S. Day 3rd, Chuck H.J. Ziolkowski, Dominic A. Scudiero, Sharon A. Meyer, Anthony S. Lubiniecki, Anthony Joseph Girardi, Sheila Margaret Galloway, Gaither D. Bynum;
Defective repair of alkylated DNA by human tumour and SV40-transformed human cell strains.
Nature 288:724-727(1980)

PubMed=7273335; DOI=10.1093/carcin/2.6.567
Louise Simon, Royce M. Hazard, Veronica M. Maher, J. Justin McCormick;
Enhanced cell killing and mutagenesis by ethylnitrosourea in xeroderma pigmentosum cells.
Carcinogenesis 2:567-570(1981)

PubMed=7163956; DOI=10.1007/BF01543020
James Edward Cleaver;
Rapid complementation method for classifying excision repair-defective xeroderma pigmentosum cell strains.
Somatic Cell Genet. 8:801-810(1982)

PubMed=6307543; DOI=10.1093/carcin/4.8.1075
Ian A. Teo, Alan R. Lehmann, R. Muller, Manfred Fedor Rajewsky;
Similar rate of O6-ethylguanine elimination from DNA in normal human fibroblast and xeroderma pigmentosum cell strains not transformed by SV40.
Carcinogenesis 4:1075-1077(1983)

PubMed=2823132; DOI=10.1016/0167-8817(87)90024-1
Ljiljana Vuksanovic, James Edward Cleaver;
Unique cross-link and monoadduct repair characteristics of a xeroderma pigmentosum revertant cell line.
Mutat. Res. 184:255-263(1987)

PubMed=3118197; DOI=10.1128/mcb.7.9.3353-3357.1987; PMCID=PMC367978
James Edward Cleaver, Felipe Cortes, Louise H. Lutze-Mann, William F. Morgan, Audrey N. Player, David L. Mitchell;
Unique DNA repair properties of a xeroderma pigmentosum revertant.
Mol. Cell. Biol. 7:3353-3357(1987)

PubMed=1702221; DOI=10.1073/pnas.87.24.9908; PMCID=PMC55283
Ichiro Satokata, Kiyoji Tanaka, Naoyuki Miura, Iwai Miyamoto, Yoshiaki Satoh, Seiji Kondo, Yoshio Okada;
Characterization of a splicing mutation in group A xeroderma pigmentosum.
Proc. Natl. Acad. Sci. U.S.A. 87:9908-9912(1990)

PubMed=1372102; DOI=10.1016/0921-8777(92)90080-M
Ichiro Satokata, Kiyoji Tanaka, Naoyuki Miura, Masashi Narita, Takashi Mimaki, Yoshiaki Satoh, Seiji Kondo, Yoshio Okada;
Three nonsense mutations responsible for group A xeroderma pigmentosum.
Mutat. Res. 273:193-202(1992)

PubMed=1549511; DOI=10.1093/nar/20.5.991; PMCID=PMC312081
Christopher J. Jones, James Edward Cleaver, Richard Dean Wood;
Repair of damaged DNA by extracts from a xeroderma pigmentosum complementation group A revertant and expression of a protein absent in its parental cell line.
Nucleic Acids Res. 20:991-995(1992)

PubMed=8464385; DOI=10.1093/mutage/8.2.155
Mindy L. McDowell, Thai Nguyen, James Edward Cleaver;
A single-site mutation in the XPAC gene alters photoproduct recognition.
Mutagenesis 8:155-161(1993)

PubMed=7519740; DOI=10.1016/0165-7992(94)90014-0
Christopher J. Jones, R. Stephen Lloyd, Richard Dean Wood;
Analysis of cells harboring a putative DNA repair gene reveals a lack of evidence for a second independent xeroderma pigmentosum group A correcting gene.
Mutat. Res. 324:159-164(1994)

PubMed=8055625; DOI=10.1093/carcin/15.8.1493
Mauro Mezzina, Eric Eveno, Odile Chevallier-Lagente, Annie Benoit, Madeleine Carreau, Wim Vermeulen, Jan Hendrik Jozef Hoeijmakers, Miria Stefanini, Alan R. Lehmann, Christine A. Weber, Alain Sarasin;
Correction by the ERCC2 gene of UV sensitivity and repair deficiency phenotype in a subset of trichothiodystrophy cells.
Carcinogenesis 15:1493-1498(1994)

PubMed=7671243
Eric Eveno, Francois Bourre, Xavier Quilliet, Odile Chevallier-Lagente, Len Roza, Andre P.M. Eker, Wim J. Kleijer, Osamu Nikaido, Miria Stefanini, Jan Hendrik Jozef Hoeijmakers, Dirk Bootsma ...Show all 14 authors... , James Edward Cleaver, Alain Sarasin, Mauro Mezzina; Show fewer authors
Different removal of ultraviolet photoproducts in genetically related xeroderma pigmentosum and trichothiodystrophy diseases.
Cancer Res. 55:4325-4332(1995)

PubMed=9415314; DOI=10.1038/sj.gt.3300495
Lin Zeng, Xavier Quilliet, Odile Chevallier-Lagente, Eric Eveno, Alain Sarasin, Mauro Mezzina;
Retrovirus-mediated gene transfer corrects DNA repair defect of xeroderma pigmentosum cells of complementation groups A, B and C.
Gene Ther. 4:1077-1084(1997)

PubMed=10334196; DOI=10.1093/carcin/20.5.799
Mark O'Driscoll, Simone Martinelli, Carmela Ciotta, Peter Karran;
Combined mismatch and nucleotide excision repair defects in a human cell line: mismatch repair processes methylation but not UV- or ionizing radiation-induced DNA damage.
Carcinogenesis 20:799-804(1999)

Cross-references
Encyclopedic resources Wikidata; Q98135282
Entry history
Entry creation07-Sep-2018
Last entry update19-Dec-2024
Version number10