Literature DB >> 3627143

Hypersensitivity of Bloom's syndrome fibroblasts to N-ethyl-N-nitrosourea.

T Kurihara, M Inoue, K Tatsumi.   

Abstract

Fibroblast cells from two Japanese patients with Bloom's syndrome (BS) and normal donors were studied for the inactivation of colony-forming ability and the induction of sister-chromatid exchanges (SCEs) after N-ethyl-N-nitrosourea (ENU) treatment. The reduction of ENU-induced SCEs as a function of post-treatment incubation time was also compared between BS and normal fibroblasts. BS cells were approximately 4 times more sensitive than normal cells to the lethal effect of ENU and remarkably hypersensitive to the SCE induction by ENU. The post-treatment incubation of ENU-treated normal cells in the fresh medium resulted in a time-dependent decrease of the SCE level until 6 h after which time the SCE level remained the plateau of about 50% of the initial level. In contrast, the ENU-induced SCEs in BS cells decreased much more slowly with post-treatment incubation time and its half life was 24 h. These results collectively support the view that BS cells may be defective in the rapid repair of certain type(s) of DNA damages induced by ENU.

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Year:  1987        PMID: 3627143     DOI: 10.1016/0167-8817(87)90071-x

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


  7 in total

1.  rqh1+, a fission yeast gene related to the Bloom's and Werner's syndrome genes, is required for reversible S phase arrest.

Authors:  E Stewart; C R Chapman; F Al-Khodairy; A M Carr; T Enoch
Journal:  EMBO J       Date:  1997-05-15       Impact factor: 11.598

2.  Evolution of the RECQ family of helicases: A drosophila homolog, Dmblm, is similar to the human bloom syndrome gene.

Authors:  K Kusano; M E Berres; W R Engels
Journal:  Genetics       Date:  1999-03       Impact factor: 4.562

3.  Chromosomal breakage, endomitosis, endoreduplication, and hypersensitivity toward radiomimetric and alkylating agents: a possible new autosomal recessive mutation in a girl with craniosynostosis and microcephaly.

Authors:  N Tommerup; E Mortensen; M H Nielsen; R D Wegner; D Schindler; M Mikkelsen
Journal:  Hum Genet       Date:  1993-10       Impact factor: 4.132

4.  Bloom syndrome: an analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1.

Authors:  J German; A M Roe; M F Leppert; N A Ellis
Journal:  Proc Natl Acad Sci U S A       Date:  1994-07-05       Impact factor: 11.205

5.  An interaction between the mammalian DNA repair protein XRCC1 and DNA ligase III.

Authors:  K W Caldecott; C K McKeown; J D Tucker; S Ljungquist; L H Thompson
Journal:  Mol Cell Biol       Date:  1994-01       Impact factor: 4.272

6.  DNA ligase III is the major high molecular weight DNA joining activity in SV40-transformed human fibroblasts: normal levels of DNA ligase III activity in Bloom syndrome cells.

Authors:  A E Tomkinson; R Starr; R A Schultz
Journal:  Nucleic Acids Res       Date:  1993-11-25       Impact factor: 16.971

7.  Transition of phenotypic dimorphism with regard to spontaneous sister chromatid exchange in Epstein-Barr virus-transformed Bloom's syndrome lymphoblastoid cell lines.

Authors:  K Tatsumi; T Kurihara; I Arita; J Tatsumi-Miyajima
Journal:  Jpn J Cancer Res       Date:  1992-07
  7 in total

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