Literature DB >> 7955052

DNA replication arrest and tolerance to DNA methylation damage.

N Zhukovskaya1, P Branch, G Aquilina, P Karran.   

Abstract

Inhibition of DNA replication by different DNA damaging agents has been investigated in HeLaMR cells and a methylation damage-tolerant variant HeLa5A1. In synchronous HeLaMR and HeLa5A1 cells exposed to N-ethyl-N-nitrosourea or ionizing radiation in mid-G1 phase, DNA synthesis was inhibited in the following S phase. N-methyl-N-nitrosourea-induced replication inhibition in HeLaMR cells was delayed until the second S phase after treatment. In contrast, N-methyl-N-nitrosourea treatment of HeLa5A1 cells affected neither the timing nor the extent of the first or second S phases. Both radiation and chemical treatment inhibited replication of an episomal plasmid and of genomic DNA in unison. Inhibition was observed at levels of DNA damage that did not directly damage the plasmid molecules. Thus, DNA replication inhibition occurs immediately after ionizing radiation or ethylation damage, but methylation damage requires processing through one cell cycle to generate an inhibitory signal. The inhibitory signal appears to act in trans on undamaged DNA. Although methylation-tolerant cells are responsive to inhibition after gamma-irradiation, methylation damage does not produce inhibitory signals to which they respond.

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Year:  1994        PMID: 7955052     DOI: 10.1093/carcin/15.10.2189

Source DB:  PubMed          Journal:  Carcinogenesis        ISSN: 0143-3334            Impact factor:   4.944


  8 in total

1.  ATR kinase activation mediated by MutSalpha and MutLalpha in response to cytotoxic O6-methylguanine adducts.

Authors:  Ken-ichi Yoshioka; Yoshiko Yoshioka; Peggy Hsieh
Journal:  Mol Cell       Date:  2006-05-19       Impact factor: 17.970

Review 2.  Methylating agents and DNA repair responses: Methylated bases and sources of strand breaks.

Authors:  Michael D Wyatt; Douglas L Pittman
Journal:  Chem Res Toxicol       Date:  2006-12       Impact factor: 3.739

3.  The Major Replicative Histone Chaperone CAF-1 Suppresses the Activity of the DNA Mismatch Repair System in the Cytotoxic Response to a DNA-methylating Agent.

Authors:  Lyudmila Y Kadyrova; Basanta K Dahal; Farid A Kadyrov
Journal:  J Biol Chem       Date:  2016-11-21       Impact factor: 5.157

4.  Methylator-induced, mismatch repair-dependent G2 arrest is activated through Chk1 and Chk2.

Authors:  Aaron W Adamson; Dillon I Beardsley; Wan-Ju Kim; Yajuan Gao; R Baskaran; Kevin D Brown
Journal:  Mol Biol Cell       Date:  2005-01-12       Impact factor: 4.138

5.  Mismatch repair-dependent processing of methylation damage gives rise to persistent single-stranded gaps in newly replicated DNA.

Authors:  Nina Mojas; Massimo Lopes; Josef Jiricny
Journal:  Genes Dev       Date:  2007-12-15       Impact factor: 11.361

6.  Mismatch repair-dependent G2 checkpoint induced by low doses of SN1 type methylating agents requires the ATR kinase.

Authors:  Lovorka Stojic; Nina Mojas; Petr Cejka; Massimiliano Di Pietro; Stefano Ferrari; Giancarlo Marra; Josef Jiricny
Journal:  Genes Dev       Date:  2004-06-01       Impact factor: 11.361

7.  Dose-dependent spatiotemporal responses of mammalian cells to an alkylating agent.

Authors:  Ann Rancourt; Sachiko Sato; Masahiko S Satoh
Journal:  PLoS One       Date:  2019-03-29       Impact factor: 3.240

Review 8.  DNA replication: stable driving prevents fatal smashes.

Authors:  A D Donaldson; J J Blow
Journal:  Curr Biol       Date:  2001-11-27       Impact factor: 10.834

  8 in total

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