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The distinctive signatures of promoter regions and operon junctions across prokaryotes

Here we show that regions upstream of first transcribed genes have oligonucleotide signatures that distinguish them from regions upstream of genes in the middle of operons. Databases of experimentally confirmed transcription units do not exist for most genomes. Thus, to expand the analyses into geno...

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Autores principales: Janga, Sarath Chandra, Lamboy, Warren F., Huerta, Araceli M., Moreno-Hagelsieb, Gabriel
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1557821/
https://www.ncbi.nlm.nih.gov/pubmed/16914446
http://dx.doi.org/10.1093/nar/gkl563
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author Janga, Sarath Chandra
Lamboy, Warren F.
Huerta, Araceli M.
Moreno-Hagelsieb, Gabriel
author_facet Janga, Sarath Chandra
Lamboy, Warren F.
Huerta, Araceli M.
Moreno-Hagelsieb, Gabriel
author_sort Janga, Sarath Chandra
collection PubMed
description Here we show that regions upstream of first transcribed genes have oligonucleotide signatures that distinguish them from regions upstream of genes in the middle of operons. Databases of experimentally confirmed transcription units do not exist for most genomes. Thus, to expand the analyses into genomes with no experimentally confirmed data, we used genes conserved adjacent in evolutionarily distant genomes as representatives of genes inside operons. Likewise, we used divergently transcribed genes as representative examples of first transcribed genes. In model organisms, the trinucleotide signatures of regions upstream of these representative genes allow for operon predictions with accuracies close to those obtained with known operon data (0.8). Signature-based operon predictions have more similar phylogenetic profiles and higher proportions of genes in the same pathways than predicted transcription unit boundaries (TUBs). These results confirm that we are separating genes with related functions, as expected for operons, from genes not necessarily related, as expected for genes in different transcription units. We also test the quality of the predictions using microarray data in six genomes and show that the signature-predicted operons tend to have high correlations of expression. Oligonucleotide signatures should expand the number of tools available to identify operons even in poorly characterized genomes.
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spelling pubmed-15578212006-09-06 The distinctive signatures of promoter regions and operon junctions across prokaryotes Janga, Sarath Chandra Lamboy, Warren F. Huerta, Araceli M. Moreno-Hagelsieb, Gabriel Nucleic Acids Res Computational Biology Here we show that regions upstream of first transcribed genes have oligonucleotide signatures that distinguish them from regions upstream of genes in the middle of operons. Databases of experimentally confirmed transcription units do not exist for most genomes. Thus, to expand the analyses into genomes with no experimentally confirmed data, we used genes conserved adjacent in evolutionarily distant genomes as representatives of genes inside operons. Likewise, we used divergently transcribed genes as representative examples of first transcribed genes. In model organisms, the trinucleotide signatures of regions upstream of these representative genes allow for operon predictions with accuracies close to those obtained with known operon data (0.8). Signature-based operon predictions have more similar phylogenetic profiles and higher proportions of genes in the same pathways than predicted transcription unit boundaries (TUBs). These results confirm that we are separating genes with related functions, as expected for operons, from genes not necessarily related, as expected for genes in different transcription units. We also test the quality of the predictions using microarray data in six genomes and show that the signature-predicted operons tend to have high correlations of expression. Oligonucleotide signatures should expand the number of tools available to identify operons even in poorly characterized genomes. Oxford University Press 2006 2006-08-12 /pmc/articles/PMC1557821/ /pubmed/16914446 http://dx.doi.org/10.1093/nar/gkl563 Text en © 2006 The Author(s).
spellingShingle Computational Biology
Janga, Sarath Chandra
Lamboy, Warren F.
Huerta, Araceli M.
Moreno-Hagelsieb, Gabriel
The distinctive signatures of promoter regions and operon junctions across prokaryotes
title The distinctive signatures of promoter regions and operon junctions across prokaryotes
title_full The distinctive signatures of promoter regions and operon junctions across prokaryotes
title_fullStr The distinctive signatures of promoter regions and operon junctions across prokaryotes
title_full_unstemmed The distinctive signatures of promoter regions and operon junctions across prokaryotes
title_short The distinctive signatures of promoter regions and operon junctions across prokaryotes
title_sort distinctive signatures of promoter regions and operon junctions across prokaryotes
topic Computational Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1557821/
https://www.ncbi.nlm.nih.gov/pubmed/16914446
http://dx.doi.org/10.1093/nar/gkl563
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