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NagR(Bt) Is a Pleiotropic and Dual Transcriptional Regulator in Bacillus thuringiensis
NagR, belonging to the GntR/HutC family, is a negative regulator that directly represses the nagP and nagAB genes, which are involved in GlcNAc transport and utilization in Bacillus subtilis. Our previous work confirmed that the chitinase B gene (chiB) of Bacillus thuringiensis strain Bti75 is also...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6141813/ https://www.ncbi.nlm.nih.gov/pubmed/30254611 http://dx.doi.org/10.3389/fmicb.2018.01899 |
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author | Cao, Zhang-lei Tan, Tong-tong Zhang, Yan-li Han, Lu Hou, Xiao-yue Ma, Hui-yong Cai, Jun |
author_facet | Cao, Zhang-lei Tan, Tong-tong Zhang, Yan-li Han, Lu Hou, Xiao-yue Ma, Hui-yong Cai, Jun |
author_sort | Cao, Zhang-lei |
collection | PubMed |
description | NagR, belonging to the GntR/HutC family, is a negative regulator that directly represses the nagP and nagAB genes, which are involved in GlcNAc transport and utilization in Bacillus subtilis. Our previous work confirmed that the chitinase B gene (chiB) of Bacillus thuringiensis strain Bti75 is also negatively controlled by YvoA(Bt), the ortholog of NagR from B. subtilis. In this work, we investigated its regulatory network in Bti75 and found that YvoA(Bt) is an N-acetylglucosamine utilization regulator primarily involved in GlcNAc catabolism; therefore YvoA(Bt) is renamed as NagR(Bt). The RNA-seq data revealed that 27 genes were upregulated and 14 genes were downregulated in the ΔnagR mutant compared with the wild-type strain. The regulon (exponential phase) was characterized by RNA-seq, bioinformatics software, electrophoretic mobility shift assays, and quantitative real-time reverse transcription PCR. In the Bti75 genome, 19 genes that were directly regulated and 30 genes that were indirectly regulated by NagR(Bt) were identified. We compiled in silico, in vitro, and in vivo evidence that NagR(Bt) behaves as a repressor and activator to directly or indirectly influence major biological processes involved in amino sugar metabolism, nucleotide metabolism, fatty acid metabolism, phosphotransferase system, and the Embden–Meyerhof–Parnas pathway. |
format | Online Article Text |
id | pubmed-6141813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61418132018-09-25 NagR(Bt) Is a Pleiotropic and Dual Transcriptional Regulator in Bacillus thuringiensis Cao, Zhang-lei Tan, Tong-tong Zhang, Yan-li Han, Lu Hou, Xiao-yue Ma, Hui-yong Cai, Jun Front Microbiol Microbiology NagR, belonging to the GntR/HutC family, is a negative regulator that directly represses the nagP and nagAB genes, which are involved in GlcNAc transport and utilization in Bacillus subtilis. Our previous work confirmed that the chitinase B gene (chiB) of Bacillus thuringiensis strain Bti75 is also negatively controlled by YvoA(Bt), the ortholog of NagR from B. subtilis. In this work, we investigated its regulatory network in Bti75 and found that YvoA(Bt) is an N-acetylglucosamine utilization regulator primarily involved in GlcNAc catabolism; therefore YvoA(Bt) is renamed as NagR(Bt). The RNA-seq data revealed that 27 genes were upregulated and 14 genes were downregulated in the ΔnagR mutant compared with the wild-type strain. The regulon (exponential phase) was characterized by RNA-seq, bioinformatics software, electrophoretic mobility shift assays, and quantitative real-time reverse transcription PCR. In the Bti75 genome, 19 genes that were directly regulated and 30 genes that were indirectly regulated by NagR(Bt) were identified. We compiled in silico, in vitro, and in vivo evidence that NagR(Bt) behaves as a repressor and activator to directly or indirectly influence major biological processes involved in amino sugar metabolism, nucleotide metabolism, fatty acid metabolism, phosphotransferase system, and the Embden–Meyerhof–Parnas pathway. Frontiers Media S.A. 2018-09-11 /pmc/articles/PMC6141813/ /pubmed/30254611 http://dx.doi.org/10.3389/fmicb.2018.01899 Text en Copyright © 2018 Cao, Tan, Zhang, Han, Hou, Ma and Cai. 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) and the copyright owner(s) 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 Cao, Zhang-lei Tan, Tong-tong Zhang, Yan-li Han, Lu Hou, Xiao-yue Ma, Hui-yong Cai, Jun NagR(Bt) Is a Pleiotropic and Dual Transcriptional Regulator in Bacillus thuringiensis |
title | NagR(Bt) Is a Pleiotropic and Dual Transcriptional Regulator in Bacillus thuringiensis |
title_full | NagR(Bt) Is a Pleiotropic and Dual Transcriptional Regulator in Bacillus thuringiensis |
title_fullStr | NagR(Bt) Is a Pleiotropic and Dual Transcriptional Regulator in Bacillus thuringiensis |
title_full_unstemmed | NagR(Bt) Is a Pleiotropic and Dual Transcriptional Regulator in Bacillus thuringiensis |
title_short | NagR(Bt) Is a Pleiotropic and Dual Transcriptional Regulator in Bacillus thuringiensis |
title_sort | nagr(bt) is a pleiotropic and dual transcriptional regulator in bacillus thuringiensis |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6141813/ https://www.ncbi.nlm.nih.gov/pubmed/30254611 http://dx.doi.org/10.3389/fmicb.2018.01899 |
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