Literature DB >> 9628366

Dependence of McrBC cleavage on distance between recognition elements.

F J Stewart1, E A Raleigh.   

Abstract

DNA cleavage by the modification-dependent restriction enzyme McrBC requires the presence of two suitably modified recognition elements appropriately spaced in the substrate. To characterize the spacing requirement in more detail, we have constructed a plasmid with a single McrBC cleavage site, in which the distance between recognition elements could be systematically varied while preserving the local sequence surrounding the recognition elements. Optimal separation between elements was 55-103 basepairs, with detectable cleavage observed at spacing of 32 bp to 2 kb; no cleavage was seen with spacing of 22 bp or less or with 3 kb between elements. Changing the spacing by 4 basepairs within the optimal range had little effect on the efficiency of cleavage, suggesting that the recognition elements need not lie on the same face of the DNA helix.

Mesh:

Substances:

Year:  1998        PMID: 9628366

Source DB:  PubMed          Journal:  Biol Chem        ISSN: 1431-6730            Impact factor:   3.915


  33 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.  The McrBC restriction endonuclease assembles into a ring structure in the presence of G nucleotides.

Authors:  D Panne; S A Müller; S Wirtz; A Engel; T A Bickle
Journal:  EMBO J       Date:  2001-06-15       Impact factor: 11.598

3.  A comprehensive analysis of allelic methylation status of CpG islands on human chromosome 21q.

Authors:  Yoichi Yamada; Hidemi Watanabe; Fumihito Miura; Hidenobu Soejima; Michiko Uchiyama; Tsuyoshi Iwasaka; Tsunehiro Mukai; Yoshiyuki Sakaki; Takashi Ito
Journal:  Genome Res       Date:  2004-02       Impact factor: 9.043

4.  A parent-of-origin detectable polymorphism in the hypermethylated region upstream of the human H19 gene.

Authors:  Nori Nakayashiki; Jun Kanetake; Yasuhiro Aoki
Journal:  Int J Legal Med       Date:  2004-02-13       Impact factor: 2.686

5.  McrBs, a modulator peptide for McrBC activity.

Authors:  D Panne; E A Raleigh; T A Bickle
Journal:  EMBO J       Date:  1998-09-15       Impact factor: 11.598

6.  DNA methylation in lysogens of pathogenic Burkholderia spp. requires prophage induction and is restricted to excised phage DNA.

Authors:  M J Smith; J A Jeddeloh
Journal:  J Bacteriol       Date:  2005-02       Impact factor: 3.490

Review 7.  Structure and function of type II restriction endonucleases.

Authors:  A Pingoud; A Jeltsch
Journal:  Nucleic Acids Res       Date:  2001-09-15       Impact factor: 16.971

8.  Cloning, purification and initial characterization of E. coli McrA, a putative 5-methylcytosine-specific nuclease.

Authors:  Elizabeth A Mulligan; John J Dunn
Journal:  Protein Expr Purif       Date:  2008-07-10       Impact factor: 1.650

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.  Differential binding of Escherichia coli McrA protein to DNA sequences that contain the dinucleotide m5CpG.

Authors:  Elizabeth A Mulligan; Eli Hatchwell; Sean R McCorkle; John J Dunn
Journal:  Nucleic Acids Res       Date:  2009-12-16       Impact factor: 16.971

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.