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Movement of DNA sequence recognition domains between non-orthologous proteins
Comparisons of proteins show that they evolve through the movement of domains. However, in many cases, the underlying mechanisms remain unclear. Here, we observed the movements of DNA recognition domains between non-orthologous proteins within a prokaryote genome. Restriction–modification (RM) syste...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467074/ https://www.ncbi.nlm.nih.gov/pubmed/22821560 http://dx.doi.org/10.1093/nar/gks681 |
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author | Furuta, Yoshikazu Kobayashi, Ichizo |
author_facet | Furuta, Yoshikazu Kobayashi, Ichizo |
author_sort | Furuta, Yoshikazu |
collection | PubMed |
description | Comparisons of proteins show that they evolve through the movement of domains. However, in many cases, the underlying mechanisms remain unclear. Here, we observed the movements of DNA recognition domains between non-orthologous proteins within a prokaryote genome. Restriction–modification (RM) systems, consisting of a sequence-specific DNA methyltransferase and a restriction enzyme, contribute to maintenance/evolution of genomes/epigenomes. RM systems limit horizontal gene transfer but are themselves mobile. We compared Type III RM systems in Helicobacter pylori genomes and found that target recognition domain (TRD) sequences are mobile, moving between different orthologous groups that occupy unique chromosomal locations. Sequence comparisons suggested that a likely underlying mechanism is movement through homologous recombination of similar DNA sequences that encode amino acid sequence motifs that are conserved among Type III DNA methyltransferases. Consistent with this movement, incongruence was observed between the phylogenetic trees of TRD regions and other regions in proteins. Horizontal acquisition of diverse TRD sequences was suggested by detection of homologs in other Helicobacter species and distantly related bacterial species. One of these RM systems in H. pylori was inactivated by insertion of another RM system that likely transferred from an oral bacterium. TRD movement represents a novel route for diversification of DNA-interacting proteins. |
format | Online Article Text |
id | pubmed-3467074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-34670742012-10-10 Movement of DNA sequence recognition domains between non-orthologous proteins Furuta, Yoshikazu Kobayashi, Ichizo Nucleic Acids Res Nucleic Acid Enzymes Comparisons of proteins show that they evolve through the movement of domains. However, in many cases, the underlying mechanisms remain unclear. Here, we observed the movements of DNA recognition domains between non-orthologous proteins within a prokaryote genome. Restriction–modification (RM) systems, consisting of a sequence-specific DNA methyltransferase and a restriction enzyme, contribute to maintenance/evolution of genomes/epigenomes. RM systems limit horizontal gene transfer but are themselves mobile. We compared Type III RM systems in Helicobacter pylori genomes and found that target recognition domain (TRD) sequences are mobile, moving between different orthologous groups that occupy unique chromosomal locations. Sequence comparisons suggested that a likely underlying mechanism is movement through homologous recombination of similar DNA sequences that encode amino acid sequence motifs that are conserved among Type III DNA methyltransferases. Consistent with this movement, incongruence was observed between the phylogenetic trees of TRD regions and other regions in proteins. Horizontal acquisition of diverse TRD sequences was suggested by detection of homologs in other Helicobacter species and distantly related bacterial species. One of these RM systems in H. pylori was inactivated by insertion of another RM system that likely transferred from an oral bacterium. TRD movement represents a novel route for diversification of DNA-interacting proteins. Oxford University Press 2012-10 2012-07-20 /pmc/articles/PMC3467074/ /pubmed/22821560 http://dx.doi.org/10.1093/nar/gks681 Text en © The Author(s) 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Nucleic Acid Enzymes Furuta, Yoshikazu Kobayashi, Ichizo Movement of DNA sequence recognition domains between non-orthologous proteins |
title | Movement of DNA sequence recognition domains between non-orthologous proteins |
title_full | Movement of DNA sequence recognition domains between non-orthologous proteins |
title_fullStr | Movement of DNA sequence recognition domains between non-orthologous proteins |
title_full_unstemmed | Movement of DNA sequence recognition domains between non-orthologous proteins |
title_short | Movement of DNA sequence recognition domains between non-orthologous proteins |
title_sort | movement of dna sequence recognition domains between non-orthologous proteins |
topic | Nucleic Acid Enzymes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467074/ https://www.ncbi.nlm.nih.gov/pubmed/22821560 http://dx.doi.org/10.1093/nar/gks681 |
work_keys_str_mv | AT furutayoshikazu movementofdnasequencerecognitiondomainsbetweennonorthologousproteins AT kobayashiichizo movementofdnasequencerecognitiondomainsbetweennonorthologousproteins |