Literature DB >> 28516862

Non-essential MCM-related proteins mediate a response to DNA damage in the archaeon Methanococcus maripaludis.

Alison D Walters1,2, James P J Chong1.   

Abstract

The single minichromosome maintenance (MCM) protein found in most archaea has been widely studied as a simplified model for the MCM complex that forms the catalytic core of the eukaryotic replicative helicase. Organisms of the order Methanococcales are unusual in possessing multiple MCM homologues. The Methanococcus maripaludis S2 genome encodes four MCM homologues, McmA-McmD. DNA helicase assays reveal that the unwinding activity of the three MCM-like proteins is highly variable despite sequence similarities and suggests additional motifs that influence MCM function are yet to be identified. While the gene encoding McmA could not be deleted, strains harbouring individual deletions of genes encoding each of the other MCMs display phenotypes consistent with these proteins modulating DNA damage responses. M. maripaludis S2 is the first archaeon in which MCM proteins have been shown to influence the DNA damage response.

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Year:  2017        PMID: 28516862      PMCID: PMC5737143          DOI: 10.1099/mic.0.000460

Source DB:  PubMed          Journal:  Microbiology (Reading)        ISSN: 1350-0872            Impact factor:   2.777


  50 in total

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3.  Organization of the archaeal MCM complex on DNA and implications for the helicase mechanism.

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Review 4.  Extra-chromosomal elements and the evolution of cellular DNA replication machineries.

Authors:  Adam T McGeoch; Stephen D Bell
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Review 5.  The Mcm complex: unwinding the mechanism of a replicative helicase.

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Journal:  Microbiol Mol Biol Rev       Date:  2009-12       Impact factor: 11.056

6.  Genome-scale analysis of gene function in the hydrogenotrophic methanogenic archaeon Methanococcus maripaludis.

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7.  Chromosome replication and the division cycle of Escherichia coli B/r.

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10.  Excess Mcm2-7 license dormant origins of replication that can be used under conditions of replicative stress.

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Journal:  J Cell Biol       Date:  2006-06-05       Impact factor: 10.539

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