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Regulation and overexpression studies of YidC in Mycobacterium tuberculosis
The preprotein translocase, YidC is an envelope protein which controls respiratory metabolism in Mycobacterium tuberculosis. Previously, we have established that depletion of yidC is deleterious for both extra- and intracellular proliferation of M. tuberculosis; however, it remains unclear how YidC...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244158/ https://www.ncbi.nlm.nih.gov/pubmed/30459465 http://dx.doi.org/10.1038/s41598-018-35475-4 |
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author | Thakur, Preeti Choudhary, Eira Pareek, Madhu Agarwal, Nisheeth |
author_facet | Thakur, Preeti Choudhary, Eira Pareek, Madhu Agarwal, Nisheeth |
author_sort | Thakur, Preeti |
collection | PubMed |
description | The preprotein translocase, YidC is an envelope protein which controls respiratory metabolism in Mycobacterium tuberculosis. Previously, we have established that depletion of yidC is deleterious for both extra- and intracellular proliferation of M. tuberculosis; however, it remains unclear how YidC expression is regulated under different growth conditions and whether its altered expression impact mycobacterial physiology. Herein, we show that yidC is expressed as an operon with upstream genes. Interestingly, expression analysis under various stress conditions reveals a distinct paradox in the profile of the yidC mRNA transcripts and the YidC protein. While YidC protein level is moderately elevated upon bacterial exposure to cell surface stresses, the corresponding mRNA transcript levels are significantly repressed under these conditions. In contrast, overexpression of M. tuberculosis yidC under a strong anhydrotetracycline-inducible promoter results in significant induction of YidC protein. Additionally, we also observe that overexpression of M. tuberculosis yidC, and not of its counterpart from fast-growing M. smegmatis, results in altered in vitro growth of bacteria, compromised integrity of bacterial cell envelope and differential expression of a small set of genes including those which are regulated under detergent stress. Overall findings of our study suggest that YidC proteins of slow- and fast-growing mycobacteria are functionally distinct despite exhibiting a great deal of identity. |
format | Online Article Text |
id | pubmed-6244158 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62441582018-11-27 Regulation and overexpression studies of YidC in Mycobacterium tuberculosis Thakur, Preeti Choudhary, Eira Pareek, Madhu Agarwal, Nisheeth Sci Rep Article The preprotein translocase, YidC is an envelope protein which controls respiratory metabolism in Mycobacterium tuberculosis. Previously, we have established that depletion of yidC is deleterious for both extra- and intracellular proliferation of M. tuberculosis; however, it remains unclear how YidC expression is regulated under different growth conditions and whether its altered expression impact mycobacterial physiology. Herein, we show that yidC is expressed as an operon with upstream genes. Interestingly, expression analysis under various stress conditions reveals a distinct paradox in the profile of the yidC mRNA transcripts and the YidC protein. While YidC protein level is moderately elevated upon bacterial exposure to cell surface stresses, the corresponding mRNA transcript levels are significantly repressed under these conditions. In contrast, overexpression of M. tuberculosis yidC under a strong anhydrotetracycline-inducible promoter results in significant induction of YidC protein. Additionally, we also observe that overexpression of M. tuberculosis yidC, and not of its counterpart from fast-growing M. smegmatis, results in altered in vitro growth of bacteria, compromised integrity of bacterial cell envelope and differential expression of a small set of genes including those which are regulated under detergent stress. Overall findings of our study suggest that YidC proteins of slow- and fast-growing mycobacteria are functionally distinct despite exhibiting a great deal of identity. Nature Publishing Group UK 2018-11-20 /pmc/articles/PMC6244158/ /pubmed/30459465 http://dx.doi.org/10.1038/s41598-018-35475-4 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Thakur, Preeti Choudhary, Eira Pareek, Madhu Agarwal, Nisheeth Regulation and overexpression studies of YidC in Mycobacterium tuberculosis |
title | Regulation and overexpression studies of YidC in Mycobacterium tuberculosis |
title_full | Regulation and overexpression studies of YidC in Mycobacterium tuberculosis |
title_fullStr | Regulation and overexpression studies of YidC in Mycobacterium tuberculosis |
title_full_unstemmed | Regulation and overexpression studies of YidC in Mycobacterium tuberculosis |
title_short | Regulation and overexpression studies of YidC in Mycobacterium tuberculosis |
title_sort | regulation and overexpression studies of yidc in mycobacterium tuberculosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244158/ https://www.ncbi.nlm.nih.gov/pubmed/30459465 http://dx.doi.org/10.1038/s41598-018-35475-4 |
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