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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
Der Kaloustian V.M., de Weerd-Kastelein E.A., Kleijer W.J., Keijzer W., Bootsma D.
The genetic defect in the de Sanctis-Cacchione syndrome.
J. Invest. Dermatol. 63:392-396(1974)

PubMed=6256643; DOI=10.1038/288724a0
Day R.S. 3rd, Ziolkowski C.H.J., Scudiero D.A., Meyer S.A., Lubiniecki A.S., Girardi A.J., Galloway S.M., Bynum G.D.
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
Simon L., Hazard R.M., Maher V.M., McCormick J.J.
Enhanced cell killing and mutagenesis by ethylnitrosourea in xeroderma pigmentosum cells.
Carcinogenesis 2:567-570(1981)

PubMed=7163956; DOI=10.1007/BF01543020
Cleaver J.E.
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
Teo I.A., Lehmann A.R., Muller R., Rajewsky M.F.
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
Vuksanovic L., Cleaver J.E.
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
Cleaver J.E., Cortes F., Lutze-Mann L.H., Morgan W.F., Player A.N., Mitchell D.L.
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
Satokata I., Tanaka K., Miura N., Miyamoto I., Satoh Y., Kondo S., Okada Y.
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
Satokata I., Tanaka K., Miura N., Narita M., Mimaki T., Satoh Y., Kondo S., Okada Y.
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
Jones C.J., Cleaver J.E., Wood R.D.
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
McDowell M.L., Nguyen T., Cleaver J.E.
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
Jones C.J., Lloyd R.S., Wood R.D.
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
Mezzina M., Eveno E., Chevallier-Lagente O., Benoit A., Carreau M., Vermeulen W., Hoeijmakers J.H.J., Stefanini M., Lehmann A.R., Weber C.A., Sarasin A.
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
Eveno E., Bourre F., Quilliet X., Chevallier-Lagente O., Roza L., Eker A.P.M., Kleijer W.J., Nikaido O., Stefanini M., Hoeijmakers J.H.J., Bootsma D., Cleaver J.E., Sarasin A., Mezzina M.
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
Zeng L., Quilliet X., Chevallier-Lagente O., Eveno E., Sarasin A., Mezzina M.
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
O'Driscoll M., Martinelli S., Ciotta C., Karran P.
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