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Functional Diversity of Transcriptional Regulators in the Cyanobacterium Synechocystis sp. PCC 6803

Functions of transcriptional regulators (TRs) are still poorly understood in the model cyanobacterium Synechocystis sp. PCC 6803. To address the issue, we constructed knockout mutants for 32 putative TR-encoding genes of Synechocystis, and comparatively analyzed their phenotypes under autotrophic gr...

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Autores principales: Shi, Mengliang, Zhang, Xiaoqing, Pei, Guangsheng, Chen, Lei, Zhang, Weiwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318462/
https://www.ncbi.nlm.nih.gov/pubmed/28270809
http://dx.doi.org/10.3389/fmicb.2017.00280
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author Shi, Mengliang
Zhang, Xiaoqing
Pei, Guangsheng
Chen, Lei
Zhang, Weiwen
author_facet Shi, Mengliang
Zhang, Xiaoqing
Pei, Guangsheng
Chen, Lei
Zhang, Weiwen
author_sort Shi, Mengliang
collection PubMed
description Functions of transcriptional regulators (TRs) are still poorly understood in the model cyanobacterium Synechocystis sp. PCC 6803. To address the issue, we constructed knockout mutants for 32 putative TR-encoding genes of Synechocystis, and comparatively analyzed their phenotypes under autotrophic growth condition and metabolic profiles using liquid chromatography-mass spectrometry-based metabolomics. The results showed that only four mutants of TR genes, sll1872 (lytR), slr0741 (phoU), slr0395 (ntcB), and slr1871 (pirR), showed differential growth patterns in BG11 medium when compared with the wild type; however, in spite of no growth difference observed for the remaining TR mutants, metabolomic profiling showed that they were different at the metabolite level, suggesting significant functional diversity of TRs in Synechocystis. In addition, an integrative metabolomic and gene families’ analysis of all TR mutants led to the identification of five pairs of TR genes that each shared close relationship in both gene families and metabolomic clustering trees, suggesting possible conserved functions of these TRs during evolution. Moreover, more than a dozen pairs of TR genes with different origin and evolution were found with similar metabolomic profiles, suggesting a possible functional convergence of the TRs during genome evolution. Finally, a protein–protein network analysis was performed to predict regulatory targets of TRs, allowing inference of possible regulatory gene targets for 4 out of five pairs of TRs. This study provided new insights into the regulatory functions and evolution of TR genes in Synechocystis.
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spelling pubmed-53184622017-03-07 Functional Diversity of Transcriptional Regulators in the Cyanobacterium Synechocystis sp. PCC 6803 Shi, Mengliang Zhang, Xiaoqing Pei, Guangsheng Chen, Lei Zhang, Weiwen Front Microbiol Microbiology Functions of transcriptional regulators (TRs) are still poorly understood in the model cyanobacterium Synechocystis sp. PCC 6803. To address the issue, we constructed knockout mutants for 32 putative TR-encoding genes of Synechocystis, and comparatively analyzed their phenotypes under autotrophic growth condition and metabolic profiles using liquid chromatography-mass spectrometry-based metabolomics. The results showed that only four mutants of TR genes, sll1872 (lytR), slr0741 (phoU), slr0395 (ntcB), and slr1871 (pirR), showed differential growth patterns in BG11 medium when compared with the wild type; however, in spite of no growth difference observed for the remaining TR mutants, metabolomic profiling showed that they were different at the metabolite level, suggesting significant functional diversity of TRs in Synechocystis. In addition, an integrative metabolomic and gene families’ analysis of all TR mutants led to the identification of five pairs of TR genes that each shared close relationship in both gene families and metabolomic clustering trees, suggesting possible conserved functions of these TRs during evolution. Moreover, more than a dozen pairs of TR genes with different origin and evolution were found with similar metabolomic profiles, suggesting a possible functional convergence of the TRs during genome evolution. Finally, a protein–protein network analysis was performed to predict regulatory targets of TRs, allowing inference of possible regulatory gene targets for 4 out of five pairs of TRs. This study provided new insights into the regulatory functions and evolution of TR genes in Synechocystis. Frontiers Media S.A. 2017-02-21 /pmc/articles/PMC5318462/ /pubmed/28270809 http://dx.doi.org/10.3389/fmicb.2017.00280 Text en Copyright © 2017 Shi, Zhang, Pei, Chen and Zhang. 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
Shi, Mengliang
Zhang, Xiaoqing
Pei, Guangsheng
Chen, Lei
Zhang, Weiwen
Functional Diversity of Transcriptional Regulators in the Cyanobacterium Synechocystis sp. PCC 6803
title Functional Diversity of Transcriptional Regulators in the Cyanobacterium Synechocystis sp. PCC 6803
title_full Functional Diversity of Transcriptional Regulators in the Cyanobacterium Synechocystis sp. PCC 6803
title_fullStr Functional Diversity of Transcriptional Regulators in the Cyanobacterium Synechocystis sp. PCC 6803
title_full_unstemmed Functional Diversity of Transcriptional Regulators in the Cyanobacterium Synechocystis sp. PCC 6803
title_short Functional Diversity of Transcriptional Regulators in the Cyanobacterium Synechocystis sp. PCC 6803
title_sort functional diversity of transcriptional regulators in the cyanobacterium synechocystis sp. pcc 6803
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5318462/
https://www.ncbi.nlm.nih.gov/pubmed/28270809
http://dx.doi.org/10.3389/fmicb.2017.00280
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