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Census of solo LuxR genes in prokaryotic genomes
luxR genes encode transcriptional regulators that control acyl homoserine lactone-based quorum sensing (AHL QS) in Gram negative bacteria. On the bacterial chromosome, luxR genes are usually found next or near to a luxI gene encoding the AHL signal synthase. Recently, a number of luxR genes were des...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4357305/ https://www.ncbi.nlm.nih.gov/pubmed/25815274 http://dx.doi.org/10.3389/fcimb.2015.00020 |
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author | Hudaiberdiev, Sanjarbek Choudhary, Kumari S. Vera Alvarez, Roberto Gelencsér, Zsolt Ligeti, Balázs Lamba, Doriano Pongor, Sándor |
author_facet | Hudaiberdiev, Sanjarbek Choudhary, Kumari S. Vera Alvarez, Roberto Gelencsér, Zsolt Ligeti, Balázs Lamba, Doriano Pongor, Sándor |
author_sort | Hudaiberdiev, Sanjarbek |
collection | PubMed |
description | luxR genes encode transcriptional regulators that control acyl homoserine lactone-based quorum sensing (AHL QS) in Gram negative bacteria. On the bacterial chromosome, luxR genes are usually found next or near to a luxI gene encoding the AHL signal synthase. Recently, a number of luxR genes were described that have no luxI genes in their vicinity on the chromosome. These so-called solo luxR genes may either respond to internal AHL signals produced by a non-adjacent luxI in the chromosome, or can respond to exogenous signals. Here we present a survey of solo luxR genes found in complete and draft bacterial genomes in the NCBI databases using HMMs. We found that 2698 of the 3550 luxR genes found are solos, which is an unexpectedly high number even if some of the hits may be false positives. We also found that solo LuxR sequences form distinct clusters that are different from the clusters of LuxR sequences that are part of the known luxR-luxI topological arrangements. We also found a number of cases that we termed twin luxR topologies, in which two adjacent luxR genes were in tandem or divergent orientation. Many of the luxR solo clusters were devoid of the sequence motifs characteristic of AHL binding LuxR proteins so there is room to speculate that the solos may be involved in sensing hitherto unknown signals. It was noted that only some of the LuxR clades are rich in conserved cysteine residues. Molecular modeling suggests that some of the cysteines may be involved in disulfide formation, which makes us speculate that some LuxR proteins, including some of the solos may be involved in redox regulation. |
format | Online Article Text |
id | pubmed-4357305 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-43573052015-03-26 Census of solo LuxR genes in prokaryotic genomes Hudaiberdiev, Sanjarbek Choudhary, Kumari S. Vera Alvarez, Roberto Gelencsér, Zsolt Ligeti, Balázs Lamba, Doriano Pongor, Sándor Front Cell Infect Microbiol Microbiology luxR genes encode transcriptional regulators that control acyl homoserine lactone-based quorum sensing (AHL QS) in Gram negative bacteria. On the bacterial chromosome, luxR genes are usually found next or near to a luxI gene encoding the AHL signal synthase. Recently, a number of luxR genes were described that have no luxI genes in their vicinity on the chromosome. These so-called solo luxR genes may either respond to internal AHL signals produced by a non-adjacent luxI in the chromosome, or can respond to exogenous signals. Here we present a survey of solo luxR genes found in complete and draft bacterial genomes in the NCBI databases using HMMs. We found that 2698 of the 3550 luxR genes found are solos, which is an unexpectedly high number even if some of the hits may be false positives. We also found that solo LuxR sequences form distinct clusters that are different from the clusters of LuxR sequences that are part of the known luxR-luxI topological arrangements. We also found a number of cases that we termed twin luxR topologies, in which two adjacent luxR genes were in tandem or divergent orientation. Many of the luxR solo clusters were devoid of the sequence motifs characteristic of AHL binding LuxR proteins so there is room to speculate that the solos may be involved in sensing hitherto unknown signals. It was noted that only some of the LuxR clades are rich in conserved cysteine residues. Molecular modeling suggests that some of the cysteines may be involved in disulfide formation, which makes us speculate that some LuxR proteins, including some of the solos may be involved in redox regulation. Frontiers Media S.A. 2015-03-12 /pmc/articles/PMC4357305/ /pubmed/25815274 http://dx.doi.org/10.3389/fcimb.2015.00020 Text en Copyright © 2015 Hudaiberdiev, Choudhary, Vera Alvarez, Gelencsér, Ligeti, Lamba and Pongor. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Hudaiberdiev, Sanjarbek Choudhary, Kumari S. Vera Alvarez, Roberto Gelencsér, Zsolt Ligeti, Balázs Lamba, Doriano Pongor, Sándor Census of solo LuxR genes in prokaryotic genomes |
title | Census of solo LuxR genes in prokaryotic genomes |
title_full | Census of solo LuxR genes in prokaryotic genomes |
title_fullStr | Census of solo LuxR genes in prokaryotic genomes |
title_full_unstemmed | Census of solo LuxR genes in prokaryotic genomes |
title_short | Census of solo LuxR genes in prokaryotic genomes |
title_sort | census of solo luxr genes in prokaryotic genomes |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4357305/ https://www.ncbi.nlm.nih.gov/pubmed/25815274 http://dx.doi.org/10.3389/fcimb.2015.00020 |
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