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The alr-groEL1 operon in Mycobacterium tuberculosis: an interplay of multiple regulatory elements
Threonylcarbamoyladenosine is a universally conserved essential modification of tRNA that ensures translational fidelity in cellular milieu. TsaD, TsaB and TsaE are identified as tRNA-A(37)-threonylcarbamoyl (t(6)A)-transferase enzymes that have been reconstituted in vitro, in few bacteria recently....
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5335608/ https://www.ncbi.nlm.nih.gov/pubmed/28256563 http://dx.doi.org/10.1038/srep43772 |
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author | Bhat, Aadil H. Pathak, Deepika Rao, Alka |
author_facet | Bhat, Aadil H. Pathak, Deepika Rao, Alka |
author_sort | Bhat, Aadil H. |
collection | PubMed |
description | Threonylcarbamoyladenosine is a universally conserved essential modification of tRNA that ensures translational fidelity in cellular milieu. TsaD, TsaB and TsaE are identified as tRNA-A(37)-threonylcarbamoyl (t(6)A)-transferase enzymes that have been reconstituted in vitro, in few bacteria recently. However, transcriptional organization and regulation of these genes are not known in any of these organisms. This study describes the intricate architecture of a complex multicistronic alr-groEL1 operon, harboring essential genes, namely tsaD, tsaB, tsaE, groES, groEL1, and alr (required for cell wall synthesis), and rimI encoding an N-α- acetyltransferase in Mycobacterium tuberculosis. Using northern blotting, RT-PCR and in vivo fluorescence assays, genes alr to groEL1 were found to constitute an ~6.3 kb heptacistronic operon with multiple internal promoters and an I-shaped intrinsic hairpin-like cis-regulatory element. A strong promoter PtsaD within the coding sequence of rimI gene is identified in M. tuberculosis, in addition. The study further proposes an amendment in the known bicistronic groESL1 operon annotation by providing evidence that groESL1 is co-transcribed as sub-operon of alr-groEL1 operon. The architecture of alr-groEL1 operon, conservation of the genetic context and a mosaic transcriptional profile displayed under various stress conditions convincingly suggest the involvement of this operon in stress adaptation in M. tuberculosis. |
format | Online Article Text |
id | pubmed-5335608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53356082017-03-07 The alr-groEL1 operon in Mycobacterium tuberculosis: an interplay of multiple regulatory elements Bhat, Aadil H. Pathak, Deepika Rao, Alka Sci Rep Article Threonylcarbamoyladenosine is a universally conserved essential modification of tRNA that ensures translational fidelity in cellular milieu. TsaD, TsaB and TsaE are identified as tRNA-A(37)-threonylcarbamoyl (t(6)A)-transferase enzymes that have been reconstituted in vitro, in few bacteria recently. However, transcriptional organization and regulation of these genes are not known in any of these organisms. This study describes the intricate architecture of a complex multicistronic alr-groEL1 operon, harboring essential genes, namely tsaD, tsaB, tsaE, groES, groEL1, and alr (required for cell wall synthesis), and rimI encoding an N-α- acetyltransferase in Mycobacterium tuberculosis. Using northern blotting, RT-PCR and in vivo fluorescence assays, genes alr to groEL1 were found to constitute an ~6.3 kb heptacistronic operon with multiple internal promoters and an I-shaped intrinsic hairpin-like cis-regulatory element. A strong promoter PtsaD within the coding sequence of rimI gene is identified in M. tuberculosis, in addition. The study further proposes an amendment in the known bicistronic groESL1 operon annotation by providing evidence that groESL1 is co-transcribed as sub-operon of alr-groEL1 operon. The architecture of alr-groEL1 operon, conservation of the genetic context and a mosaic transcriptional profile displayed under various stress conditions convincingly suggest the involvement of this operon in stress adaptation in M. tuberculosis. Nature Publishing Group 2017-03-03 /pmc/articles/PMC5335608/ /pubmed/28256563 http://dx.doi.org/10.1038/srep43772 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Bhat, Aadil H. Pathak, Deepika Rao, Alka The alr-groEL1 operon in Mycobacterium tuberculosis: an interplay of multiple regulatory elements |
title | The alr-groEL1 operon in Mycobacterium tuberculosis: an interplay of multiple regulatory elements |
title_full | The alr-groEL1 operon in Mycobacterium tuberculosis: an interplay of multiple regulatory elements |
title_fullStr | The alr-groEL1 operon in Mycobacterium tuberculosis: an interplay of multiple regulatory elements |
title_full_unstemmed | The alr-groEL1 operon in Mycobacterium tuberculosis: an interplay of multiple regulatory elements |
title_short | The alr-groEL1 operon in Mycobacterium tuberculosis: an interplay of multiple regulatory elements |
title_sort | alr-groel1 operon in mycobacterium tuberculosis: an interplay of multiple regulatory elements |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5335608/ https://www.ncbi.nlm.nih.gov/pubmed/28256563 http://dx.doi.org/10.1038/srep43772 |
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