Literature DB >> 7112349

Isolation of UV-sensitive mutants of mouse L5178Y cells by a cell suspension spotting method.

T Shiomi, N Hieda-Shiomi, K Sato.   

Abstract

We have isolated 56 UV-sensitive mutant clones from a mouse L51 T/t line of L5178Y cells by a cell suspension spotting method. Five mutants have also been isolated from L51 T/t and L5178Y cells by the method reported by Thompson and coworkers (22). We divided the mutants into two groups, "highly sensitive" and "moderately sensitive" mutants, according to their sensitivity to UV irradiation. Fifty-eight mutants were highly sensitive and three were moderately sensitive to UV. The reconstruction experiments indicate that more than 90% of highly sensitive mutants were recovered by the cell suspension spotting method. Frequencies of recovered mutants highly sensitive to UV increased with increasing dose of mutagens. Recovered mutant frequency reached 10(-2) after treatment with 1.5 micrograms/ml of N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) (survival 0.2%). Eight UV-sensitive mutants were divided into four complementation groups. These mutants were 2-6 times more sensitive to UV than parental L51 T/t cells in terms of D37 (dose required to reduce survival to 37%). Four representative UV-sensitive mutants which are classified into different complementation groups were examined for their sensitivity to killing by UV, 4-nitroquinoline-1-oxide (4NQO), mitomycin C (MMC), X-rays, and MNNG. All four classes of mutants were found to be cross-sensitive to UV, 4NQO, and MMC, but not sensitive to X-rays and MNNG.

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Year:  1982        PMID: 7112349     DOI: 10.1007/bf01538891

Source DB:  PubMed          Journal:  Somatic Cell Genet        ISSN: 0098-0366


  4 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.  Rodent UV-sensitive mutant cell lines in complementation groups 6-10 have normal general excision repair activity.

Authors:  J T Reardon; L H Thompson; A Sancar
Journal:  Nucleic Acids Res       Date:  1997-03-01       Impact factor: 16.971

3.  Human chromosome 13 compensates a DNA repair defect in UV-sensitive mouse cells by mouse--human cell hybridization.

Authors:  T Hori; T Shiomi; K Sato
Journal:  Proc Natl Acad Sci U S A       Date:  1983-09       Impact factor: 11.205

4.  UVs syndrome, a new general category of photosensitive disorder with defective DNA repair, is distinct from xeroderma pigmentosum variant and rodent complementation group I.

Authors:  T Itoh; Y Fujiwara; T Ono; M Yamaizumi
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

  4 in total

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