Literature DB >> 1734285

Type III restriction enzymes need two inversely oriented recognition sites for DNA cleavage.

A Meisel1, T A Bickle, D H Krüger, C Schroeder.   

Abstract

Type III restriction/modification enzyme recognize short, non-palindromic sequences that can be methylated on only one strand, with the paradoxical consequence that during replication of what is in effect hemimethylated DNA totally unmodified sites arise. Why the unmodified sites are not subject to suicidal restriction was not clear. Here we show that restriction requires two unmodified recognition sites that can be separated by different distances but which must be in inverse orientation. All of the unmodified sites in newly replicated DNA are of course in the same orientation, which explains why they are not restricted. This result may be of relevance to other manifestations of anisotropy in double-stranded DNA, such as genetic imprinting.

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Year:  1992        PMID: 1734285     DOI: 10.1038/355467a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  62 in total

Review 1.  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

2.  Functional cooperation between exonucleases and endonucleases--basis for the evolution of restriction enzymes.

Authors:  Nidhanapathi K Raghavendra; Desirazu N Rao
Journal:  Nucleic Acids Res       Date:  2003-04-01       Impact factor: 16.971

3.  DNA supercoiling enables the type IIS restriction enzyme BspMI to recognise the relative orientation of two DNA sequences.

Authors:  Isabel J Kingston; Niall A Gormley; Stephen E Halford
Journal:  Nucleic Acids Res       Date:  2003-09-15       Impact factor: 16.971

4.  DNA communications by Type III restriction endonucleases--confirmation of 1D translocation over 3D looping.

Authors:  Luke J Peakman; Mark D Szczelkun
Journal:  Nucleic Acids Res       Date:  2004-08-09       Impact factor: 16.971

5.  Type III restriction enzymes cleave DNA by long-range interaction between sites in both head-to-head and tail-to-tail inverted repeat.

Authors:  Kara van Aelst; Júlia Tóth; Subramanian P Ramanathan; Friedrich W Schwarz; Ralf Seidel; Mark D Szczelkun
Journal:  Proc Natl Acad Sci U S A       Date:  2010-04-30       Impact factor: 11.205

6.  Short-range and long-range context effects on coliphage T4 endonuclease II-dependent restriction.

Authors:  K Carlson; L D Kosturko; A C Nyström
Journal:  J Bacteriol       Date:  1996-11       Impact factor: 3.490

7.  Type III restriction is alleviated by bacteriophage (RecE) homologous recombination function but enhanced by bacterial (RecBCD) function.

Authors:  Naofumi Handa; Ichizo Kobayashi
Journal:  J Bacteriol       Date:  2005-11       Impact factor: 3.490

8.  Unidirectional translocation from recognition site and a necessary interaction with DNA end for cleavage by Type III restriction enzyme.

Authors:  Nidhanapati K Raghavendra; Desirazu N Rao
Journal:  Nucleic Acids Res       Date:  2004-10-22       Impact factor: 16.971

9.  Type III restriction enzymes communicate in 1D without looping between their target sites.

Authors:  Subramanian P Ramanathan; Kara van Aelst; Alice Sears; Luke J Peakman; Fiona M Diffin; Mark D Szczelkun; Ralf Seidel
Journal:  Proc Natl Acad Sci U S A       Date:  2009-01-30       Impact factor: 11.205

10.  Genome of bacteriophage P1.

Authors:  Małgorzata B Łobocka; Debra J Rose; Guy Plunkett; Marek Rusin; Arkadiusz Samojedny; Hansjörg Lehnherr; Michael B Yarmolinsky; Frederick R Blattner
Journal:  J Bacteriol       Date:  2004-11       Impact factor: 3.490

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