Towards a more accurate annotation of tyrosine-based site-specific recombinases in bacterial genomes

<p>Abstract</p> <p>Background</p> <p>Tyrosine-based site-specific recombinases (TBSSRs) are DNA breaking-rejoining enzymes. In bacterial genomes, they play a major role in the comings and goings of mobile genetic elements (MGEs), such as temperate phage genomes, integra...

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Main Authors: Van Houdt Rob, Leplae Raphael, Lima-Mendez Gipsi, Mergeay Max, Toussaint Ariane
Format: Article
Language:English
Published: BMC 2012-04-01
Series:Mobile DNA
Online Access:http://www.mobilednajournal.com/content/3/1/6
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spelling doaj-d0baf609e2414140870390ea1b0364732020-11-24T21:28:04ZengBMCMobile DNA1759-87532012-04-0131610.1186/1759-8753-3-6Towards a more accurate annotation of tyrosine-based site-specific recombinases in bacterial genomesVan Houdt RobLeplae RaphaelLima-Mendez GipsiMergeay MaxToussaint Ariane<p>Abstract</p> <p>Background</p> <p>Tyrosine-based site-specific recombinases (TBSSRs) are DNA breaking-rejoining enzymes. In bacterial genomes, they play a major role in the comings and goings of mobile genetic elements (MGEs), such as temperate phage genomes, integrated conjugative elements (ICEs) or integron cassettes. TBSSRs are also involved in the segregation of plasmids and chromosomes, the resolution of plasmid dimers and of co-integrates resulting from the replicative transposition of transposons. With the aim of improving the annotation of TBSSR genes in genomic sequences and databases, which so far is far from robust, we built a set of over 1,300 TBSSR protein sequences tagged with their genome of origin. We organized them in families to investigate: i) whether TBSSRs tend to be more conserved within than between classes of MGE types and ii) whether the (sub)families may help in understanding more about the function of TBSSRs associated in tandem or trios on plasmids and chromosomes.</p> <p>Results</p> <p>A total of 67% of the TBSSRs in our set are MGE type specific. We define a new class of actinobacterial transposons, related to Tn<it>554</it>, containing one abnormally long TBSSR and one of typical size, and we further characterize numerous TBSSRs trios present in plasmids and chromosomes of α- and β-proteobacteria.</p> <p>Conclusions</p> <p>The simple <it>in silico </it>procedure described here, which uses a set of reference TBSSRs from defined MGE types, could contribute to greatly improve the annotation of tyrosine-based site-specific recombinases in plasmid, (pro)phage and other integrated MGE genomes. It also reveals TBSSRs families whose distribution among bacterial taxa suggests they mediate lateral gene transfer.</p> http://www.mobilednajournal.com/content/3/1/6
collection DOAJ
language English
format Article
sources DOAJ
author Van Houdt Rob
Leplae Raphael
Lima-Mendez Gipsi
Mergeay Max
Toussaint Ariane
spellingShingle Van Houdt Rob
Leplae Raphael
Lima-Mendez Gipsi
Mergeay Max
Toussaint Ariane
Towards a more accurate annotation of tyrosine-based site-specific recombinases in bacterial genomes
Mobile DNA
author_facet Van Houdt Rob
Leplae Raphael
Lima-Mendez Gipsi
Mergeay Max
Toussaint Ariane
author_sort Van Houdt Rob
title Towards a more accurate annotation of tyrosine-based site-specific recombinases in bacterial genomes
title_short Towards a more accurate annotation of tyrosine-based site-specific recombinases in bacterial genomes
title_full Towards a more accurate annotation of tyrosine-based site-specific recombinases in bacterial genomes
title_fullStr Towards a more accurate annotation of tyrosine-based site-specific recombinases in bacterial genomes
title_full_unstemmed Towards a more accurate annotation of tyrosine-based site-specific recombinases in bacterial genomes
title_sort towards a more accurate annotation of tyrosine-based site-specific recombinases in bacterial genomes
publisher BMC
series Mobile DNA
issn 1759-8753
publishDate 2012-04-01
description <p>Abstract</p> <p>Background</p> <p>Tyrosine-based site-specific recombinases (TBSSRs) are DNA breaking-rejoining enzymes. In bacterial genomes, they play a major role in the comings and goings of mobile genetic elements (MGEs), such as temperate phage genomes, integrated conjugative elements (ICEs) or integron cassettes. TBSSRs are also involved in the segregation of plasmids and chromosomes, the resolution of plasmid dimers and of co-integrates resulting from the replicative transposition of transposons. With the aim of improving the annotation of TBSSR genes in genomic sequences and databases, which so far is far from robust, we built a set of over 1,300 TBSSR protein sequences tagged with their genome of origin. We organized them in families to investigate: i) whether TBSSRs tend to be more conserved within than between classes of MGE types and ii) whether the (sub)families may help in understanding more about the function of TBSSRs associated in tandem or trios on plasmids and chromosomes.</p> <p>Results</p> <p>A total of 67% of the TBSSRs in our set are MGE type specific. We define a new class of actinobacterial transposons, related to Tn<it>554</it>, containing one abnormally long TBSSR and one of typical size, and we further characterize numerous TBSSRs trios present in plasmids and chromosomes of α- and β-proteobacteria.</p> <p>Conclusions</p> <p>The simple <it>in silico </it>procedure described here, which uses a set of reference TBSSRs from defined MGE types, could contribute to greatly improve the annotation of tyrosine-based site-specific recombinases in plasmid, (pro)phage and other integrated MGE genomes. It also reveals TBSSRs families whose distribution among bacterial taxa suggests they mediate lateral gene transfer.</p>
url http://www.mobilednajournal.com/content/3/1/6
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