Literature DB >> 4000167

Genetic complementation between UV-sensitive CHO mutants and xeroderma pigmentosum fibroblasts.

L H Thompson, C L Mooney, K W Brookman.   

Abstract

The purpose of this study was to determine the feasibility of doing complementation analysis between DNA-repair mutants of CHO cells and human fibroblasts based on the recovery of hybrid cells resistant to DNA damage. Two UV-sensitive CHO mutant lines, UV20 and UV41, which belong to different genetic complementation groups, were fused with fibroblasts of xeroderma pigmentosum in various complementation groups. Selection for complementing hybrids was performed using a combination of ouabain to kill the XP cells and mitomycin C to kill the CHO mutants. Because the frequency of viable hybrid clones was generally less than 10(-6) and the frequency of revertants of each CHO mutant was approximately 2 X 10(-7), putative hybrids required verification. The hybrid character of clones was established by testing for the presence of human DNA in a dot-blot procedure. Hybrid clones were obtained from 9 of the 10 different crosses involving 5 complementation groups of XP cells. The 4 attempted crosses with 2 other XP groups yielded no hybrid colonies. Thus, a definitive complementation analysis was not possible. Hybrids were evaluated for their UV resistance using a rapid assay that measures differential cytotoxicity (DC). All 9 hybrids were more resistant than the parental mutant CHO and XP cells, indicating that in each case complementation of the CHO repair defect by a human gene had occurred. 3 hybrids were analyzed for their UV-radiation survival curves and shown to be much more resistant that the CHO mutants but less resistant than normal CHO cells. With 2 of these hybrids, sensitive subclones, which had presumably lost the complementing gene, were found to have similar sensitivity to the parental CHO mutants. We conclude that the extremely low frequency of viable hybrids in this system limits the usefulness of the approach. The possibility remains that each of the nonhybridizing XP strains could be altered in the same locus as one of the CHO mutants.

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Year:  1985        PMID: 4000167     DOI: 10.1016/0027-5107(85)90139-3

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  14 in total

1.  Molecular cloning of the human DNA excision repair gene ERCC-6.

Authors:  C Troelstra; H Odijk; J de Wit; A Westerveld; L H Thompson; D Bootsma; J H Hoeijmakers
Journal:  Mol Cell Biol       Date:  1990-11       Impact factor: 4.272

2.  Molecular cloning and characterization of a mammalian excision repair gene that partially restores UV resistance to xeroderma pigmentosum complementation group D cells.

Authors:  J E Arrand; N M Bone; R T Johnson
Journal:  Proc Natl Acad Sci U S A       Date:  1989-09       Impact factor: 11.205

3.  Molecular cloning and biological characterization of the human excision repair gene ERCC-3.

Authors:  G Weeda; R C van Ham; R Masurel; A Westerveld; H Odijk; J de Wit; D Bootsma; A J van der Eb; J H Hoeijmakers
Journal:  Mol Cell Biol       Date:  1990-06       Impact factor: 4.272

4.  Molecular cloning and biological characterization of a human gene, ERCC2, that corrects the nucleotide excision repair defect in CHO UV5 cells.

Authors:  C A Weber; E P Salazar; S A Stewart; L H Thompson
Journal:  Mol Cell Biol       Date:  1988-03       Impact factor: 4.272

5.  ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs.

Authors:  K W Brookman; J E Lamerdin; M P Thelen; M Hwang; J T Reardon; A Sancar; Z Q Zhou; C A Walter; C N Parris; L H Thompson
Journal:  Mol Cell Biol       Date:  1996-11       Impact factor: 4.272

6.  An informative panel of somatic cell hybrids for physical mapping on human chromosome 19q.

Authors:  L L Bachinski; R Krahe; B F White; B Wieringa; D Shaw; R Korneluk; L H Thompson; K Johnson; M J Siciliano
Journal:  Am J Hum Genet       Date:  1993-02       Impact factor: 11.025

7.  Repair-deficient xeroderma pigmentosum cells made UV light resistant by fusion with X-ray-inactivated Chinese hamster cells.

Authors:  D Karentz; J E Cleaver
Journal:  Mol Cell Biol       Date:  1986-10       Impact factor: 4.272

8.  Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3.

Authors:  W Vermeulen; R J Scott; S Rodgers; H J Müller; J Cole; C F Arlett; W J Kleijer; D Bootsma; J H Hoeijmakers; G Weeda
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

9.  Reconstitution of mammalian excision repair activity with mutant cell-free extracts and XPAC and ERCC1 proteins expressed in Escherichia coli.

Authors:  C H Park; A Sancar
Journal:  Nucleic Acids Res       Date:  1993-11-11       Impact factor: 16.971

10.  Human chromosome 15 confers partial complementation of phenotypes to xeroderma pigmentosum group F cells.

Authors:  P J Saxon; R A Schultz; E J Stanbridge; E C Friedberg
Journal:  Am J Hum Genet       Date:  1989-04       Impact factor: 11.025

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