Literature DB >> 10536161

Molecular evolution of DNA-(cytosine-N4) methyltransferases: evidence for their polyphyletic origin.

J M Bujnicki1, M Radlinska.   

Abstract

DNA N4-cytosine methyltransferases (N4mC MTases) are a family of S-adenosyl-L-methionine (AdoMet)-dependent MTases. Members of this family were previously found to share nine conserved sequence motifs, but the evolutionary basis of these similarities has never been studied in detail. We performed phylogenetic analysis of 37 known and potential new family members from the multiple sequence alignment using distance matrix, parsimony and maximum likelihood approaches to infer the evolutionary relationship among the N4mC MTases and classify them into groups of orthologs. All the treeing algorithms employed as well as results of exhaustive sequence database searching support a scenario, in which the majority of N4mC MTases, except for M. Bal I and M. Bam HI, arose by divergence from a common ancestor. Interestingly, MTases M. Bal I and M. Bam HI apparently originated from N6-adenine MTases and represent the most recent addendum to the N4mC MTase family. In addition to the previously reported nine sequence motifs, two more conserved sequence patches were detected. Phylogenetic analysis also provided the evidence for massive horizontal transfer of MTase genes, presumably with the whole restriction-modification systems, between Bacteria and Archaea.

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Year:  1999        PMID: 10536161      PMCID: PMC148735          DOI: 10.1093/nar/27.22.4501

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  23 in total

1.  DNA binding properties in vivo and target recognition domain sequence alignment analyses of wild-type and mutant RsrI [N6-adenine] DNA methyltransferases.

Authors:  S S Szegedi; R I Gumport
Journal:  Nucleic Acids Res       Date:  2000-10-15       Impact factor: 16.971

2.  Functional analysis of MmeI from methanol utilizer Methylophilus methylotrophus, a subtype IIC restriction-modification enzyme related to type I enzymes.

Authors:  Joanna Nakonieczna; Tadeusz Kaczorowski; Agnieszka Obarska-Kosinska; Janusz M Bujnicki
Journal:  Appl Environ Microbiol       Date:  2008-11-07       Impact factor: 4.792

3.  HemK, a class of protein methyl transferase with similarity to DNA methyl transferases, methylates polypeptide chain release factors, and hemK knockout induces defects in translational termination.

Authors:  Kenji Nakahigashi; Naoko Kubo; Shin-ichiro Narita; Takeshi Shimaoka; Simon Goto; Taku Oshima; Hirotada Mori; Maki Maeda; Chieko Wada; Hachiro Inokuchi
Journal:  Proc Natl Acad Sci U S A       Date:  2002-01-22       Impact factor: 11.205

Review 4.  Diverse functions of restriction-modification systems in addition to cellular defense.

Authors:  Kommireddy Vasu; Valakunja Nagaraja
Journal:  Microbiol Mol Biol Rev       Date:  2013-03       Impact factor: 11.056

5.  DNA methyltransferases of the cyanobacterium Anabaena PCC 7120.

Authors:  A V Matveyev; K T Young; A Meng; J Elhai
Journal:  Nucleic Acids Res       Date:  2001-04-01       Impact factor: 16.971

Review 6.  Structure, function and mechanism of exocyclic DNA methyltransferases.

Authors:  Shivakumara Bheemanaik; Yeturu V R Reddy; Desirazu N Rao
Journal:  Biochem J       Date:  2006-10-15       Impact factor: 3.857

7.  Mobility of a restriction-modification system revealed by its genetic contexts in three hosts.

Authors:  Marc Naderer; Jessica R Brust; Dieter Knowle; Robert M Blumenthal
Journal:  J Bacteriol       Date:  2002-05       Impact factor: 3.490

8.  Genetic organization and molecular analysis of the EcoVIII restriction-modification system of Escherichia coli E1585-68 and its comparison with isospecific homologs.

Authors:  Iwona Mruk; Tadeusz Kaczorowski
Journal:  Appl Environ Microbiol       Date:  2003-05       Impact factor: 4.792

Review 9.  Conflicts targeting epigenetic systems and their resolution by cell death: novel concepts for methyl-specific and other restriction systems.

Authors:  Ken Ishikawa; Eri Fukuda; Ichizo Kobayashi
Journal:  DNA Res       Date:  2010-11-08       Impact factor: 4.458

10.  Cleavage of a model DNA replication fork by a methyl-specific endonuclease.

Authors:  Ken Ishikawa; Naofumi Handa; Lauren Sears; Elisabeth A Raleigh; Ichizo Kobayashi
Journal:  Nucleic Acids Res       Date:  2011-03-26       Impact factor: 16.971

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