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Haemophilus influenzae phasevarions have evolved from type III DNA restriction systems into epigenetic regulators of gene expression
Phase variably expressed (randomly switching) methyltransferases associated with type III restriction-modification (R-M) systems have been identified in a variety of pathogenic bacteria. We have previously shown that a phase variable methyltransferase (Mod) associated with a type III R-M system in H...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1976455/ https://www.ncbi.nlm.nih.gov/pubmed/17675301 http://dx.doi.org/10.1093/nar/gkm571 |
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author | Fox, Kate L. Dowideit, Stefanie J. Erwin, Alice L. Srikhanta, Yogitha N. Smith, Arnold L. Jennings, Michael P. |
author_facet | Fox, Kate L. Dowideit, Stefanie J. Erwin, Alice L. Srikhanta, Yogitha N. Smith, Arnold L. Jennings, Michael P. |
author_sort | Fox, Kate L. |
collection | PubMed |
description | Phase variably expressed (randomly switching) methyltransferases associated with type III restriction-modification (R-M) systems have been identified in a variety of pathogenic bacteria. We have previously shown that a phase variable methyltransferase (Mod) associated with a type III R-M system in Haemophilus influenzae strain Rd coordinates the random switching of expression of multiple genes, and constitutes a phase variable regulon—‘phasevarion’. We have now identified the recognition site for the Mod methyltransferase in H. influenzae strain Rd as 5′-CGAAT-3′. This is the same recognition site as the previously described HinfIII system. A survey of 59 H. influenzae strains indicated significant sequence heterogeneity in the central, variable region of the mod gene associated with target site recognition. Intra- and inter-strain transformation experiments using Mod methylated or non-methylated plasmids, and a methylation site assay demonstrated that the sequence heterogeneity seen in the region encoding target site specificity does correlate to distinct target sites. Mutations were identified within the res gene in several strains surveyed indicating that Res is not functional. These data suggest that evolution of this type III R-M system into an epigenetic mechanism for controlling gene expression has, in some strains, resulted in loss of the DNA restriction function. |
format | Text |
id | pubmed-1976455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-19764552007-09-26 Haemophilus influenzae phasevarions have evolved from type III DNA restriction systems into epigenetic regulators of gene expression Fox, Kate L. Dowideit, Stefanie J. Erwin, Alice L. Srikhanta, Yogitha N. Smith, Arnold L. Jennings, Michael P. Nucleic Acids Res Nucleic Acid Enzymes Phase variably expressed (randomly switching) methyltransferases associated with type III restriction-modification (R-M) systems have been identified in a variety of pathogenic bacteria. We have previously shown that a phase variable methyltransferase (Mod) associated with a type III R-M system in Haemophilus influenzae strain Rd coordinates the random switching of expression of multiple genes, and constitutes a phase variable regulon—‘phasevarion’. We have now identified the recognition site for the Mod methyltransferase in H. influenzae strain Rd as 5′-CGAAT-3′. This is the same recognition site as the previously described HinfIII system. A survey of 59 H. influenzae strains indicated significant sequence heterogeneity in the central, variable region of the mod gene associated with target site recognition. Intra- and inter-strain transformation experiments using Mod methylated or non-methylated plasmids, and a methylation site assay demonstrated that the sequence heterogeneity seen in the region encoding target site specificity does correlate to distinct target sites. Mutations were identified within the res gene in several strains surveyed indicating that Res is not functional. These data suggest that evolution of this type III R-M system into an epigenetic mechanism for controlling gene expression has, in some strains, resulted in loss of the DNA restriction function. Oxford University Press 2007-08 2007-08-02 /pmc/articles/PMC1976455/ /pubmed/17675301 http://dx.doi.org/10.1093/nar/gkm571 Text en © 2007 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Nucleic Acid Enzymes Fox, Kate L. Dowideit, Stefanie J. Erwin, Alice L. Srikhanta, Yogitha N. Smith, Arnold L. Jennings, Michael P. Haemophilus influenzae phasevarions have evolved from type III DNA restriction systems into epigenetic regulators of gene expression |
title | Haemophilus influenzae phasevarions have evolved from type III DNA restriction systems into epigenetic regulators of gene expression |
title_full | Haemophilus influenzae phasevarions have evolved from type III DNA restriction systems into epigenetic regulators of gene expression |
title_fullStr | Haemophilus influenzae phasevarions have evolved from type III DNA restriction systems into epigenetic regulators of gene expression |
title_full_unstemmed | Haemophilus influenzae phasevarions have evolved from type III DNA restriction systems into epigenetic regulators of gene expression |
title_short | Haemophilus influenzae phasevarions have evolved from type III DNA restriction systems into epigenetic regulators of gene expression |
title_sort | haemophilus influenzae phasevarions have evolved from type iii dna restriction systems into epigenetic regulators of gene expression |
topic | Nucleic Acid Enzymes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1976455/ https://www.ncbi.nlm.nih.gov/pubmed/17675301 http://dx.doi.org/10.1093/nar/gkm571 |
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