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Silencing cryptic specialized metabolism in Streptomyces by the nucleoid-associated protein Lsr2
Lsr2 is a nucleoid-associated protein conserved throughout the actinobacteria, including the antibiotic-producing Streptomyces. Streptomyces species encode paralogous Lsr2 proteins (Lsr2 and Lsr2-like, or LsrL), and we show here that of the two, Lsr2 has greater functional significance. We found tha...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584129/ https://www.ncbi.nlm.nih.gov/pubmed/31215866 http://dx.doi.org/10.7554/eLife.47691 |
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author | Gehrke, Emma J Zhang, Xiafei Pimentel-Elardo, Sheila M Johnson, Andrew R Rees, Christiaan A Jones, Stephanie E Hindra, Gehrke, Sebastian S Turvey, Sonya Boursalie, Suzanne Hill, Jane E Carlson, Erin E Nodwell, Justin R Elliot, Marie A |
author_facet | Gehrke, Emma J Zhang, Xiafei Pimentel-Elardo, Sheila M Johnson, Andrew R Rees, Christiaan A Jones, Stephanie E Hindra, Gehrke, Sebastian S Turvey, Sonya Boursalie, Suzanne Hill, Jane E Carlson, Erin E Nodwell, Justin R Elliot, Marie A |
author_sort | Gehrke, Emma J |
collection | PubMed |
description | Lsr2 is a nucleoid-associated protein conserved throughout the actinobacteria, including the antibiotic-producing Streptomyces. Streptomyces species encode paralogous Lsr2 proteins (Lsr2 and Lsr2-like, or LsrL), and we show here that of the two, Lsr2 has greater functional significance. We found that Lsr2 binds AT-rich sequences throughout the chromosome, and broadly represses gene expression. Strikingly, specialized metabolic clusters were over-represented amongst its targets, and the cryptic nature of many of these clusters appears to stem from Lsr2-mediated repression. Manipulating Lsr2 activity in model species and uncharacterized isolates resulted in the production of new metabolites not seen in wild type strains. Our results suggest that the transcriptional silencing of biosynthetic clusters by Lsr2 may protect Streptomyces from the inappropriate expression of specialized metabolites, and provide global control over Streptomyces’ arsenal of signaling and antagonistic compounds. |
format | Online Article Text |
id | pubmed-6584129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-65841292019-06-21 Silencing cryptic specialized metabolism in Streptomyces by the nucleoid-associated protein Lsr2 Gehrke, Emma J Zhang, Xiafei Pimentel-Elardo, Sheila M Johnson, Andrew R Rees, Christiaan A Jones, Stephanie E Hindra, Gehrke, Sebastian S Turvey, Sonya Boursalie, Suzanne Hill, Jane E Carlson, Erin E Nodwell, Justin R Elliot, Marie A eLife Microbiology and Infectious Disease Lsr2 is a nucleoid-associated protein conserved throughout the actinobacteria, including the antibiotic-producing Streptomyces. Streptomyces species encode paralogous Lsr2 proteins (Lsr2 and Lsr2-like, or LsrL), and we show here that of the two, Lsr2 has greater functional significance. We found that Lsr2 binds AT-rich sequences throughout the chromosome, and broadly represses gene expression. Strikingly, specialized metabolic clusters were over-represented amongst its targets, and the cryptic nature of many of these clusters appears to stem from Lsr2-mediated repression. Manipulating Lsr2 activity in model species and uncharacterized isolates resulted in the production of new metabolites not seen in wild type strains. Our results suggest that the transcriptional silencing of biosynthetic clusters by Lsr2 may protect Streptomyces from the inappropriate expression of specialized metabolites, and provide global control over Streptomyces’ arsenal of signaling and antagonistic compounds. eLife Sciences Publications, Ltd 2019-06-19 /pmc/articles/PMC6584129/ /pubmed/31215866 http://dx.doi.org/10.7554/eLife.47691 Text en © 2019, Gehrke et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Microbiology and Infectious Disease Gehrke, Emma J Zhang, Xiafei Pimentel-Elardo, Sheila M Johnson, Andrew R Rees, Christiaan A Jones, Stephanie E Hindra, Gehrke, Sebastian S Turvey, Sonya Boursalie, Suzanne Hill, Jane E Carlson, Erin E Nodwell, Justin R Elliot, Marie A Silencing cryptic specialized metabolism in Streptomyces by the nucleoid-associated protein Lsr2 |
title | Silencing cryptic specialized metabolism in Streptomyces by the nucleoid-associated protein Lsr2 |
title_full | Silencing cryptic specialized metabolism in Streptomyces by the nucleoid-associated protein Lsr2 |
title_fullStr | Silencing cryptic specialized metabolism in Streptomyces by the nucleoid-associated protein Lsr2 |
title_full_unstemmed | Silencing cryptic specialized metabolism in Streptomyces by the nucleoid-associated protein Lsr2 |
title_short | Silencing cryptic specialized metabolism in Streptomyces by the nucleoid-associated protein Lsr2 |
title_sort | silencing cryptic specialized metabolism in streptomyces by the nucleoid-associated protein lsr2 |
topic | Microbiology and Infectious Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584129/ https://www.ncbi.nlm.nih.gov/pubmed/31215866 http://dx.doi.org/10.7554/eLife.47691 |
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