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PMID: 11226310 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Comparative genomics of the restriction-modification systems in Helicobacter pylori.

Lin LF, Posfai J, Roberts RJ, Kong H

Abstract

Helicobacter pylori is a Gram-negative bacterial pathogen with a small genome of 1.64-1.67 Mb. More than 20 putative DNA restriction-modification (R-M) systems, comprising more than 4% of the total genome, have been identified in the two completely sequenced H. pylori strains, 26695 and J99, based on sequence similarities. In this study, we have investigated the biochemical activities of 14 Type II R-M systems in H. pylori 26695. Less than 30% of the Type II R-M systems in 26695 are fully functional, similar to the results obtained from strain J99. Although nearly 90% of the R-M genes are shared by the two H. pylori strains, different sets of these R-M genes are functionally active in each strain. Interestingly, all strain-specific R-M genes are active, whereas most shared genes are inactive. This agrees with the notion that strain-specific genes have been acquired more recently through horizontal transfer from other bacteria and selected for function. Thus, they are less likely to be impaired by random mutations. Our results also show that H. pylori has extremely diversified R-M systems in different strains, and that the diversity may be maintained by constantly acquiring new R-M systems and by inactivating and deleting the old ones.

MeSH Terms
Cloning, Molecular DNA Methylation DNA Restriction Enzymes/genetics Genome, Bacterial Helicobacter pylori/genetics
Chemicals
DNA Restriction Enzymes
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Lin L F
New England Biolabs, Inc., 32 Tozer Road, Beverly, MA 01915, USA.
Posfai J
Roberts R J
Kong H
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
2001-02-27
Epub
2001-00-13
Pages
2740-5
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC30209
Subset
IM
Grants
NIGMS NIH HHS · GM56535 · United States
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