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Cellosaurus CS3BE-S3-G1 (CVCL_F631)

[Text version]
Cell line name CS3BE-S3-G1
Synonyms CS3BE.S3.G1; CS3BE.S3G1; CS3BEs3gl; CS3BESV; GM16094; GM1856(SV)
Accession CVCL_F631
Resource Identification Initiative To cite this cell line use: CS3BE-S3-G1 (RRID:CVCL_F631)
Comments Population: Caucasian.
Genetic integration: Method=Transfection; Gene=UniProtKB; P0A9M5; Escherichia coli gpt.
Genetic integration: Method=Transfection; Gene=UniProtKB; P03070; Simian virus 40 (SV40) large T antigen.
Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40) (Note=pSV3-gpt).
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:3439; ERCC8; Simple; p.Glu13Ter (c.37G>T); ClinVar=VCV000001716; Zygosity=Heterozygous (from parent cell line).
  • Mutation; HGNC; HGNC:3439; ERCC8; Simple; p.Ala160Val (c.479C>T); ClinVar=VCV000001717; Zygosity=Heterozygous (from parent cell line).
Disease Cockayne syndrome type A (NCIt: C135725)
Cockayne syndrome (ORDO: Orphanet_191)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_F632 (CS3BE)
Sex of cell Male
Age at sampling 13Y
Category Transformed cell line
Publications

PubMed=3002824; DOI=10.1016/0014-4827(86)90356-3
Lynne V. Mayne, Anne Priestley, Michael R. James, Julian F. Burke;
Efficient immortalization and morphological transformation of human fibroblasts by transfection with SV40 DNA linked to a dominant marker.
Exp. Cell Res. 162:530-538(1986)

PubMed=2903889; DOI=10.1080/09553008814552321
Colin Francis Arlett, Michael H.L. Green, Anne Priestley, Susan A. Harcourt, Lynne V. Mayne;
Comparative human cellular radiosensitivity: I. The effect of SV40 transformation and immortalisation on the gamma-irradiation survival of skin derived fibroblasts from normal individuals and from ataxia-telangiectasia patients and heterozygotes.
Int. J. Radiat. Biol. 54:911-928(1988)

PubMed=1339317; DOI=10.1016/0092-8674(92)90390-x
Christine Troelstra, Alain J. van Gool, Jan de Wit, Wim Vermeulen, Dirk Bootsma, Jan Hendrik Jozef Hoeijmakers;
ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes.
Cell 71:939-953(1992)

PubMed=7664335; DOI=10.1016/0092-8674(95)90028-4
Karla A. Henning, Lei Li, Narayan Iyer, Lisa D. McDaniel, Michael S. Reagan, Randy J. Legerski, Roger A. Schultz, Miria Stefanini, Alan R. Lehmann, Lynne V. Mayne, Errol Clive Friedberg;
The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH.
Cell 82:555-564(1995)

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=19329487; DOI=10.1073/pnas.0902113106; PMCID=PMC2667150
Tiziana Nardo, Roberta Oneda, Graciela Spivak, Bruno Vaz, Laurent Mortier, Pierre Thomas, Donata Orioli, Vincent Laugel, Anne Stary, Philip C. Hanawalt, Alain Sarasin, Miria Stefanini;
A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage.
Proc. Natl. Acad. Sci. U.S.A. 106:6209-6214(2009)

Cross-references
Cell line collections (Providers) Coriell; GM16094
JCRB; KURB1909
Cell line databases/resources CLO; CLO_0018853
Biological sample resources BioSample; SAMN00804326
Encyclopedic resources Wikidata; Q54848318
Entry history
Entry creation11-Feb-2013
Last entry update14-Aug-2025
Version number23