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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
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.
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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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