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PclR is a transcriptional activator of the gene that encodes the pneumococcal collagen-like protein PclA

The Gram-positive bacterium Streptococcus pneumoniae is a major human pathogen that shows high levels of genetic variability. The pneumococcal R6 genome harbours several gene clusters that are not present in all strains of the species. One of these clusters contains two divergent genes, pclA, which...

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Autores principales: Moreno-Blanco, Ana, Solano-Collado, Virtu, Ortuno-Camuñas, Alejandro, Espinosa, Manuel, Ruiz-Cruz, Sofía, Bravo, Alicia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276737/
https://www.ncbi.nlm.nih.gov/pubmed/35821046
http://dx.doi.org/10.1038/s41598-022-15758-7
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author Moreno-Blanco, Ana
Solano-Collado, Virtu
Ortuno-Camuñas, Alejandro
Espinosa, Manuel
Ruiz-Cruz, Sofía
Bravo, Alicia
author_facet Moreno-Blanco, Ana
Solano-Collado, Virtu
Ortuno-Camuñas, Alejandro
Espinosa, Manuel
Ruiz-Cruz, Sofía
Bravo, Alicia
author_sort Moreno-Blanco, Ana
collection PubMed
description The Gram-positive bacterium Streptococcus pneumoniae is a major human pathogen that shows high levels of genetic variability. The pneumococcal R6 genome harbours several gene clusters that are not present in all strains of the species. One of these clusters contains two divergent genes, pclA, which encodes a putative surface-exposed protein that contains large regions of collagen-like repeats, and spr1404 (here named pclR). PclA was shown to mediate pneumococcal adherence to host cells in vitro. In this work, we demonstrate that PclR (494 amino acids) is a transcriptional activator. It stimulates transcription of the pclA gene by binding to a specific DNA site upstream of the core promoter. In addition, we show that PclR has common features with the MgaSpn transcriptional regulator (493 amino acids), which is also encoded by the R6 genome. These proteins have high sequence similarity (60.3%), share the same organization of predicted functional domains, and generate multimeric complexes on linear double-stranded DNAs. However, on the PpclA promoter region, MgaSpn binds to a site different from the one recognized by PclR. Our results indicate that PclR and MgaSpn have similar DNA-binding properties but different DNA-binding specificities, pointing to a different regulatory role of both proteins.
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spelling pubmed-92767372022-07-14 PclR is a transcriptional activator of the gene that encodes the pneumococcal collagen-like protein PclA Moreno-Blanco, Ana Solano-Collado, Virtu Ortuno-Camuñas, Alejandro Espinosa, Manuel Ruiz-Cruz, Sofía Bravo, Alicia Sci Rep Article The Gram-positive bacterium Streptococcus pneumoniae is a major human pathogen that shows high levels of genetic variability. The pneumococcal R6 genome harbours several gene clusters that are not present in all strains of the species. One of these clusters contains two divergent genes, pclA, which encodes a putative surface-exposed protein that contains large regions of collagen-like repeats, and spr1404 (here named pclR). PclA was shown to mediate pneumococcal adherence to host cells in vitro. In this work, we demonstrate that PclR (494 amino acids) is a transcriptional activator. It stimulates transcription of the pclA gene by binding to a specific DNA site upstream of the core promoter. In addition, we show that PclR has common features with the MgaSpn transcriptional regulator (493 amino acids), which is also encoded by the R6 genome. These proteins have high sequence similarity (60.3%), share the same organization of predicted functional domains, and generate multimeric complexes on linear double-stranded DNAs. However, on the PpclA promoter region, MgaSpn binds to a site different from the one recognized by PclR. Our results indicate that PclR and MgaSpn have similar DNA-binding properties but different DNA-binding specificities, pointing to a different regulatory role of both proteins. Nature Publishing Group UK 2022-07-12 /pmc/articles/PMC9276737/ /pubmed/35821046 http://dx.doi.org/10.1038/s41598-022-15758-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Moreno-Blanco, Ana
Solano-Collado, Virtu
Ortuno-Camuñas, Alejandro
Espinosa, Manuel
Ruiz-Cruz, Sofía
Bravo, Alicia
PclR is a transcriptional activator of the gene that encodes the pneumococcal collagen-like protein PclA
title PclR is a transcriptional activator of the gene that encodes the pneumococcal collagen-like protein PclA
title_full PclR is a transcriptional activator of the gene that encodes the pneumococcal collagen-like protein PclA
title_fullStr PclR is a transcriptional activator of the gene that encodes the pneumococcal collagen-like protein PclA
title_full_unstemmed PclR is a transcriptional activator of the gene that encodes the pneumococcal collagen-like protein PclA
title_short PclR is a transcriptional activator of the gene that encodes the pneumococcal collagen-like protein PclA
title_sort pclr is a transcriptional activator of the gene that encodes the pneumococcal collagen-like protein pcla
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276737/
https://www.ncbi.nlm.nih.gov/pubmed/35821046
http://dx.doi.org/10.1038/s41598-022-15758-7
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