Literature DB >> 8420940

Repair of individual DNA strands in the hamster dihydrofolate reductase gene after treatment with ultraviolet light, alkylating agents, and cisplatin.

A May1, R S Nairn, D S Okumoto, K Wassermann, T Stevnsner, J C Jones, V A Bohr.   

Abstract

We have analyzed gene-specific and strand-specific DNA damage and repair in the dihydrofolate reductase gene in hamster cells. Cells were UV-irradiated or treated with two types of chemotherapeutics, alkylating agents or cisplatin. UV-induced pyrimidine dimers were detected using a previously published technique in which the T4 endonuclease V enzyme is used to create nicks at the lesion sites. 6-4 photoproducts were detected in a similar assay using ABC excinuclease after prior reversal of the pyrimidine dimers with photolyase. Adducts formed by the alkylating agents nitrogen mustard and dimethyl sulfate were quantitated by generating strand breaks at basic sites after neutral depurination. Cisplatin-induced intrastrand adducts were detected with ABC excinuclease, and cisplatin interstrand cross-links were detected using a denaturation-reannealing reaction before electrophoresis. In accord with previous reports by other investigators, we find distinct strand specificity of the repair of pyrimidine dimers after UV; the transcribed strand was much more efficiently repaired than the nontranscribed strand. In contrast, there was little or no strand bias in the repair of the 6-4 photoproducts. For alkylating agents, a slight bias toward repair in the transcribed strand was found after treatment with nitrogen mustard, but there appeared to be no bias in the repair after treatment with dimethyl sulfate. Cisplatin interstrand cross-links are repaired with equal efficiency from the two strands, but the more common cisplatin-induced lesion, the intrastrand adduct, is preferentially repaired from the transcribed strand. In conclusion, there is strand bias in the repair of pyrimidine dimers and cisplatin intrastrand adducts, but the strand specificity of repair may not be a general feature for all DNA lesions, as we found little or no strand bias in the repair of other lesions studied.

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Year:  1993        PMID: 8420940

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  16 in total

1.  Transcription-coupled repair is inducible in hamster cells.

Authors:  M Germanier; M Defais; V A Bohr; F Larminat
Journal:  Nucleic Acids Res       Date:  2000-12-01       Impact factor: 16.971

2.  Translocation of Cockayne syndrome group A protein to the nuclear matrix: possible relevance to transcription-coupled DNA repair.

Authors:  Shinya Kamiuchi; Masafumi Saijo; Elisabetta Citterio; Martijn de Jager; Jan H J Hoeijmakers; Kiyoji Tanaka
Journal:  Proc Natl Acad Sci U S A       Date:  2002-01-08       Impact factor: 11.205

3.  Transcription-coupled and DNA damage-dependent ubiquitination of RNA polymerase II in vitro.

Authors:  Keng-Boon Lee; Dong Wang; Stephen J Lippard; Phillip A Sharp
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-19       Impact factor: 11.205

4.  Persistent DNA damage inhibits S-phase and G2 progression, and results in apoptosis.

Authors:  D K Orren; L N Petersen; V A Bohr
Journal:  Mol Biol Cell       Date:  1997-06       Impact factor: 4.138

5.  A UV-responsive G2 checkpoint in rodent cells.

Authors:  D K Orren; L N Petersen; V A Bohr
Journal:  Mol Cell Biol       Date:  1995-07       Impact factor: 4.272

6.  The ATPase domain but not the acidic region of Cockayne syndrome group B gene product is essential for DNA repair.

Authors:  R M Brosh; A S Balajee; R R Selzer; M Sunesen; L Proietti De Santis; V A Bohr
Journal:  Mol Biol Cell       Date:  1999-11       Impact factor: 4.138

7.  Assessment of DNA damage and repair in specific genomic regions by quantitative immuno-coupled PCR.

Authors:  M F Denissenko; S Venkatachalam; E F Yamasaki; A A Wani
Journal:  Nucleic Acids Res       Date:  1994-06-25       Impact factor: 16.971

8.  Detection of platinum-DNA adducts by 32P-postlabelling.

Authors:  F A Blommaert; C P Saris
Journal:  Nucleic Acids Res       Date:  1995-04-25       Impact factor: 16.971

9.  The human CSB (ERCC6) gene corrects the transcription-coupled repair defect in the CHO cell mutant UV61.

Authors:  D K Orren; G L Dianov; V A Bohr
Journal:  Nucleic Acids Res       Date:  1996-09-01       Impact factor: 16.971

10.  Decreased transcription-coupled nucleotide excision repair capacity is associated with increased p53- and MLH1-independent apoptosis in response to cisplatin.

Authors:  Lawton J Stubbert; Jennifer M Smith; Bruce C McKay
Journal:  BMC Cancer       Date:  2010-05-14       Impact factor: 4.430

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