Literature DB >> 1833555

Mutations that confer de novo activity upon a maintenance methyltransferase.

J E Kelleher1, A S Daniel, N E Murray.   

Abstract

DNA methyltransferases are not only sequence specific in their action, but they also differentiate between the alternative methylation states of a target site. Some methyltransferases are equally active on either unmethylated or hemimethylated DNA and consequently function as de novo methyltransferases. Others are specific for hemimethylated target sequences, consistent with the postulated role of a maintenance methyltransferase in perpetuating a pattern of DNA modification. The molecular basis for the difference between de novo and maintenance methyltransferase activity is unknown, yet fundamental to cellular activities that are affected by different methylation states of the genome. The methyltransferase activity of the type I restriction and modification system, EcoK, is the only known prokaryotic methyltransferase shown to be specific for hemimethylated target sequences. We have isolated mutants of Escherichia coli K-12 which are able to modify unmethylated target sequences efficiently in a manner indicative of de novo methyltransferase activity. Consistent with this change in specificity, some mutations shift the balance between DNA restriction and modification as if both activities now compete at unmethylated targets. Two genes encode the methyltransferase and all the mutations are loosely clustered within one of them.

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Year:  1991        PMID: 1833555     DOI: 10.1016/0022-2836(91)80064-2

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  23 in total

Review 1.  Type I restriction systems: sophisticated molecular machines (a legacy of Bertani and Weigle).

Authors:  N E Murray
Journal:  Microbiol Mol Biol Rev       Date:  2000-06       Impact factor: 11.056

Review 2.  Nucleoside triphosphate-dependent restriction enzymes.

Authors:  D T Dryden; N E Murray; D N Rao
Journal:  Nucleic Acids Res       Date:  2001-09-15       Impact factor: 16.971

Review 3.  Biological function of DNA methylation.

Authors:  J Hubácek
Journal:  Folia Microbiol (Praha)       Date:  1992       Impact factor: 2.099

4.  Unusual 2-aminopurine fluorescence from a complex of DNA and the EcoKI methyltransferase.

Authors:  T-J Su; B A Connolly; C Darlington; R Mallin; D T F Dryden
Journal:  Nucleic Acids Res       Date:  2004-04-23       Impact factor: 16.971

5.  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

6.  Substrate recognition and selectivity in the type IC DNA modification methylase M.EcoR124I.

Authors:  I Taylor; D Watts; G Kneale
Journal:  Nucleic Acids Res       Date:  1993-10-25       Impact factor: 16.971

Review 7.  Biology of DNA restriction.

Authors:  T A Bickle; D H Krüger
Journal:  Microbiol Rev       Date:  1993-06

8.  Tracking EcoKI and DNA fifty years on: a golden story full of surprises.

Authors:  Wil A M Loenen
Journal:  Nucleic Acids Res       Date:  2003-12-15       Impact factor: 16.971

9.  Response to UV damage by four Escherichia coli K-12 restriction systems.

Authors:  J E Kelleher; E A Raleigh
Journal:  J Bacteriol       Date:  1994-10       Impact factor: 3.490

10.  The MmeI family: type II restriction-modification enzymes that employ single-strand modification for host protection.

Authors:  Richard D Morgan; Elizabeth A Dwinell; Tanya K Bhatia; Elizabeth M Lang; Yvette A Luyten
Journal:  Nucleic Acids Res       Date:  2009-07-03       Impact factor: 16.971

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