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RedB, a Member of the CRP/FNR Family, Functions as a Transcriptional Redox Brake
Phylogenetic and sequence similarity network analyses of the CRP (cyclic AMP receptor protein)/FNR (fumarate and nitrate reductase regulatory protein) family of transcription factors indicate the presence of numerous subgroups, many of which have not been analyzed. Five homologs of the CRP/FNR famil...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9603854/ https://www.ncbi.nlm.nih.gov/pubmed/36106751 http://dx.doi.org/10.1128/spectrum.02353-22 |
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author | Ke, Nijia Kumka, Joseph E. Fang, Mingxu Weaver, Brian Burstyn, Judith N. Bauer, Carl E. |
author_facet | Ke, Nijia Kumka, Joseph E. Fang, Mingxu Weaver, Brian Burstyn, Judith N. Bauer, Carl E. |
author_sort | Ke, Nijia |
collection | PubMed |
description | Phylogenetic and sequence similarity network analyses of the CRP (cyclic AMP receptor protein)/FNR (fumarate and nitrate reductase regulatory protein) family of transcription factors indicate the presence of numerous subgroups, many of which have not been analyzed. Five homologs of the CRP/FNR family are present in the Rhodobacter capsulatus genome. One is a member of a broadly disseminated, previously uncharacterized CRP/FNR family subgroup encoded by the gene rcc01561. In this study, we utilize mutational disruption, transcriptome sequencing (RNA-seq), and chromatin immunoprecipitation sequencing (ChIP-seq) to determine the role of RCC01561 in regulating R. capsulatus physiology. This analysis shows that a mutant strain disrupted for rcc01561 exhibits altered expression of 451 genes anaerobically. A detailed analysis of the affected loci shows that RCC01561 represses photosynthesis and favors catabolism over anabolism and the use of the Entner-Doudoroff shunt and glycolysis over that of the tricarboxylic acid (TCA) cycle to limit NADH and ATP formation. This newly characterized CRP/FNR family member with a predominant role in reducing the production of reducing potential and ATP is given the nomenclature RedB as it functions as an energy and redox brake. Beyond limiting energy production, RedB also represses the expression of numerous genes involved in protein synthesis, including those involved in translation initiation, tRNA synthesis and charging, and amino acid biosynthesis. IMPORTANCE CRP and FNR are well-characterized members of the CRP/FNR family of regulatory proteins that function to maximize cellular energy production. In this study, we identify several new subgroups of the CRP/FNR family, many of which have not yet been characterized. Using Rhodobacter capsulatus as a model, we have mutationally disrupted the gene rcc01561, which codes for a transcription factor that is a member of a unique subgroup of the CRP/FNR family. Transcriptomic analysis shows that the disruption of rcc01561 leads to the altered expression of 451 genes anaerobically. Analysis of these regulated genes indicates that RCC01561 has a novel role in limiting cellular energy production. To our knowledge, this is first example of a member of the CRP/FNR family that functions as a brake on cellular energy production. |
format | Online Article Text |
id | pubmed-9603854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-96038542022-10-27 RedB, a Member of the CRP/FNR Family, Functions as a Transcriptional Redox Brake Ke, Nijia Kumka, Joseph E. Fang, Mingxu Weaver, Brian Burstyn, Judith N. Bauer, Carl E. Microbiol Spectr Research Article Phylogenetic and sequence similarity network analyses of the CRP (cyclic AMP receptor protein)/FNR (fumarate and nitrate reductase regulatory protein) family of transcription factors indicate the presence of numerous subgroups, many of which have not been analyzed. Five homologs of the CRP/FNR family are present in the Rhodobacter capsulatus genome. One is a member of a broadly disseminated, previously uncharacterized CRP/FNR family subgroup encoded by the gene rcc01561. In this study, we utilize mutational disruption, transcriptome sequencing (RNA-seq), and chromatin immunoprecipitation sequencing (ChIP-seq) to determine the role of RCC01561 in regulating R. capsulatus physiology. This analysis shows that a mutant strain disrupted for rcc01561 exhibits altered expression of 451 genes anaerobically. A detailed analysis of the affected loci shows that RCC01561 represses photosynthesis and favors catabolism over anabolism and the use of the Entner-Doudoroff shunt and glycolysis over that of the tricarboxylic acid (TCA) cycle to limit NADH and ATP formation. This newly characterized CRP/FNR family member with a predominant role in reducing the production of reducing potential and ATP is given the nomenclature RedB as it functions as an energy and redox brake. Beyond limiting energy production, RedB also represses the expression of numerous genes involved in protein synthesis, including those involved in translation initiation, tRNA synthesis and charging, and amino acid biosynthesis. IMPORTANCE CRP and FNR are well-characterized members of the CRP/FNR family of regulatory proteins that function to maximize cellular energy production. In this study, we identify several new subgroups of the CRP/FNR family, many of which have not yet been characterized. Using Rhodobacter capsulatus as a model, we have mutationally disrupted the gene rcc01561, which codes for a transcription factor that is a member of a unique subgroup of the CRP/FNR family. Transcriptomic analysis shows that the disruption of rcc01561 leads to the altered expression of 451 genes anaerobically. Analysis of these regulated genes indicates that RCC01561 has a novel role in limiting cellular energy production. To our knowledge, this is first example of a member of the CRP/FNR family that functions as a brake on cellular energy production. American Society for Microbiology 2022-09-15 /pmc/articles/PMC9603854/ /pubmed/36106751 http://dx.doi.org/10.1128/spectrum.02353-22 Text en Copyright © 2022 Ke et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Ke, Nijia Kumka, Joseph E. Fang, Mingxu Weaver, Brian Burstyn, Judith N. Bauer, Carl E. RedB, a Member of the CRP/FNR Family, Functions as a Transcriptional Redox Brake |
title | RedB, a Member of the CRP/FNR Family, Functions as a Transcriptional Redox Brake |
title_full | RedB, a Member of the CRP/FNR Family, Functions as a Transcriptional Redox Brake |
title_fullStr | RedB, a Member of the CRP/FNR Family, Functions as a Transcriptional Redox Brake |
title_full_unstemmed | RedB, a Member of the CRP/FNR Family, Functions as a Transcriptional Redox Brake |
title_short | RedB, a Member of the CRP/FNR Family, Functions as a Transcriptional Redox Brake |
title_sort | redb, a member of the crp/fnr family, functions as a transcriptional redox brake |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9603854/ https://www.ncbi.nlm.nih.gov/pubmed/36106751 http://dx.doi.org/10.1128/spectrum.02353-22 |
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