Functional analysis of putative restriction-modification system genes in the Helicobacter pylori J99 genome
- 1 September 2000
- journal article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 28 (17) , 3216-3223
- https://doi.org/10.1093/nar/28.17.3216
Abstract
Helicobacter pylori is a gram-negative bacterium, which colonizes the gastric mucosa of humans and is implicated in a wide range of gastroduodenal diseases. The genomic sequences of two H.pylori strains, 26695 and J99, have been published recently. About two dozen potential restriction-modification (R-M) systems have been annotated in both genomes, which is far above the average number of R-M systems in other sequenced genomes. Here we describe a functional analysis of the 16 putative Type II R-M systems in the H. pylori J99 genome. To express potentially toxic endonuclease genes, a unique vector was constructed, which features repression and antisense transcription as dual control elements. To determine the methylation activities of putative DNA methyltransferases, we developed polyclonal antibodies able to detect DNA containing N6-methyladenine or N4-methylcytosine. We found that <30% of the potential Type II R-M systems in H.pylori J99 strain were fully functional, displaying both endonuclease and methyltransferase activities. Helicobacter pylori may maintain a variety of functional R-M systems, which are believed to be a primitive bacterial 'immune' system, by alternatively turning on/off a subset of numerous R-M systems.Keywords
This publication has 32 references indexed in Scilit:
- The Protein Information Resource (PIR)Nucleic Acids Research, 2000
- REBASE - restriction enzymes and methylasesNucleic Acids Research, 2000
- Genomic-sequence comparison of two unrelated isolates of the human gastric pathogen Helicobacter pyloriNature, 1999
- A family of versatile centromeric vectors designed for use in the sectoring-shuffle mutagenesis assay in Saccharomyces cerevisiaeGene, 1988
- Highly repressible expression system for cloning genes that specify potentially toxic proteinsJournal of Bacteriology, 1987
- Cloning theDdeI restriction-modification system using a two-step methodNucleic Acids Research, 1986
- Origin of replication of pBR345 plasmid DNA.Proceedings of the National Academy of Sciences, 1977
- A second specific endonuclease from Haemophilus aegyptiusJournal of Molecular Biology, 1975
- A Restriction enzyme from Hemophilus influenzaeJournal of Molecular Biology, 1970
- Temperature-sensitive regulation system of prophage lambda inductionJournal of Molecular Biology, 1967