Interplay between Nucleoid-Associated Proteins and Transcription Factors in Controlling Specialized Metabolism in <italic toggle="yes">Streptomyces</italic>

ABSTRACT Lsr2 is a small nucleoid-associated protein found throughout the actinobacteria. Lsr2 functions similarly to the well-studied H-NS, in that it preferentially binds AT-rich sequences and represses gene expression. In Streptomyces venezuelae, Lsr2 represses the expression of many specialized...

Full description

Bibliographic Details
Main Authors: Xiafei Zhang, Sara N. Andres, Marie A. Elliot
Format: Article
Language:English
Published: American Society for Microbiology 2021-08-01
Series:mBio
Subjects:
Online Access:https://journals.asm.org/doi/10.1128/mBio.01077-21
_version_ 1818922112010682368
author Xiafei Zhang
Sara N. Andres
Marie A. Elliot
author_facet Xiafei Zhang
Sara N. Andres
Marie A. Elliot
author_sort Xiafei Zhang
collection DOAJ
description ABSTRACT Lsr2 is a small nucleoid-associated protein found throughout the actinobacteria. Lsr2 functions similarly to the well-studied H-NS, in that it preferentially binds AT-rich sequences and represses gene expression. In Streptomyces venezuelae, Lsr2 represses the expression of many specialized metabolic clusters, including the chloramphenicol antibiotic biosynthetic gene cluster, and deleting lsr2 leads to significant upregulation of chloramphenicol cluster expression. We show here that Lsr2 likely exerts its repressive effects on the chloramphenicol cluster by polymerizing along the chromosome and by bridging sites within and adjacent to the chloramphenicol cluster. CmlR is a known activator of the chloramphenicol cluster, but expression of its associated gene is not upregulated in an lsr2 mutant strain. We demonstrate that CmlR is essential for chloramphenicol production, and further reveal that CmlR functions to “countersilence” Lsr2’s repressive effects by recruiting RNA polymerase and enhancing transcription, with RNA polymerase effectively clearing bound Lsr2 from the chloramphenicol cluster DNA. Our results provide insight into the interplay between opposing regulatory proteins that govern antibiotic production in S. venezuelae, which could be exploited to maximize the production of bioactive natural products in other systems. IMPORTANCE Specialized metabolic clusters in Streptomyces are the source of many clinically prescribed antibiotics. However, many clusters are not expressed in the laboratory due to repression by the nucleoid-associated protein Lsr2. Understanding how Lsr2 represses cluster expression, and how repression can be alleviated, is key to accessing the metabolic potential of these bacteria. Using the chloramphenicol biosynthetic cluster from Streptomyces venezuelae as a model, we explored the mechanistic basis underlying Lsr2-mediated repression, and activation by the pathway-specific regulator CmlR. Lsr2 polymerized along the chromosome and bridged binding sites located within and outside the cluster, promoting repression. Conversely, CmlR was essential for chloramphenicol production and further functioned to countersilence Lsr2 repression by recruiting RNA polymerase and promoting transcription, ultimately removing Lsr2 polymers from the chromosome. Manipulating the activity of both regulators led to a >130× increase in chloramphenicol levels, suggesting that combinatorial regulatory strategies can be powerful tools for maximizing natural product yields.
first_indexed 2024-12-20T01:48:21Z
format Article
id doaj.art-eb90e39b313e49a499b6c2f469974153
institution Directory Open Access Journal
issn 2150-7511
language English
last_indexed 2024-12-20T01:48:21Z
publishDate 2021-08-01
publisher American Society for Microbiology
record_format Article
series mBio
spelling doaj.art-eb90e39b313e49a499b6c2f4699741532022-12-21T19:57:42ZengAmerican Society for MicrobiologymBio2150-75112021-08-0112410.1128/mBio.01077-21Interplay between Nucleoid-Associated Proteins and Transcription Factors in Controlling Specialized Metabolism in <italic toggle="yes">Streptomyces</italic>Xiafei Zhang0Sara N. Andres1Marie A. Elliot2Department of Biology, McMaster University, Hamilton, Ontario, CanadaDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, CanadaDepartment of Biology, McMaster University, Hamilton, Ontario, CanadaABSTRACT Lsr2 is a small nucleoid-associated protein found throughout the actinobacteria. Lsr2 functions similarly to the well-studied H-NS, in that it preferentially binds AT-rich sequences and represses gene expression. In Streptomyces venezuelae, Lsr2 represses the expression of many specialized metabolic clusters, including the chloramphenicol antibiotic biosynthetic gene cluster, and deleting lsr2 leads to significant upregulation of chloramphenicol cluster expression. We show here that Lsr2 likely exerts its repressive effects on the chloramphenicol cluster by polymerizing along the chromosome and by bridging sites within and adjacent to the chloramphenicol cluster. CmlR is a known activator of the chloramphenicol cluster, but expression of its associated gene is not upregulated in an lsr2 mutant strain. We demonstrate that CmlR is essential for chloramphenicol production, and further reveal that CmlR functions to “countersilence” Lsr2’s repressive effects by recruiting RNA polymerase and enhancing transcription, with RNA polymerase effectively clearing bound Lsr2 from the chloramphenicol cluster DNA. Our results provide insight into the interplay between opposing regulatory proteins that govern antibiotic production in S. venezuelae, which could be exploited to maximize the production of bioactive natural products in other systems. IMPORTANCE Specialized metabolic clusters in Streptomyces are the source of many clinically prescribed antibiotics. However, many clusters are not expressed in the laboratory due to repression by the nucleoid-associated protein Lsr2. Understanding how Lsr2 represses cluster expression, and how repression can be alleviated, is key to accessing the metabolic potential of these bacteria. Using the chloramphenicol biosynthetic cluster from Streptomyces venezuelae as a model, we explored the mechanistic basis underlying Lsr2-mediated repression, and activation by the pathway-specific regulator CmlR. Lsr2 polymerized along the chromosome and bridged binding sites located within and outside the cluster, promoting repression. Conversely, CmlR was essential for chloramphenicol production and further functioned to countersilence Lsr2 repression by recruiting RNA polymerase and promoting transcription, ultimately removing Lsr2 polymers from the chromosome. Manipulating the activity of both regulators led to a >130× increase in chloramphenicol levels, suggesting that combinatorial regulatory strategies can be powerful tools for maximizing natural product yields.https://journals.asm.org/doi/10.1128/mBio.01077-21Streptomyceschloramphenicolantibioticcountersilencingnucleoid-associated proteinLsr2
spellingShingle Xiafei Zhang
Sara N. Andres
Marie A. Elliot
Interplay between Nucleoid-Associated Proteins and Transcription Factors in Controlling Specialized Metabolism in <italic toggle="yes">Streptomyces</italic>
mBio
Streptomyces
chloramphenicol
antibiotic
countersilencing
nucleoid-associated protein
Lsr2
title Interplay between Nucleoid-Associated Proteins and Transcription Factors in Controlling Specialized Metabolism in <italic toggle="yes">Streptomyces</italic>
title_full Interplay between Nucleoid-Associated Proteins and Transcription Factors in Controlling Specialized Metabolism in <italic toggle="yes">Streptomyces</italic>
title_fullStr Interplay between Nucleoid-Associated Proteins and Transcription Factors in Controlling Specialized Metabolism in <italic toggle="yes">Streptomyces</italic>
title_full_unstemmed Interplay between Nucleoid-Associated Proteins and Transcription Factors in Controlling Specialized Metabolism in <italic toggle="yes">Streptomyces</italic>
title_short Interplay between Nucleoid-Associated Proteins and Transcription Factors in Controlling Specialized Metabolism in <italic toggle="yes">Streptomyces</italic>
title_sort interplay between nucleoid associated proteins and transcription factors in controlling specialized metabolism in italic toggle yes streptomyces italic
topic Streptomyces
chloramphenicol
antibiotic
countersilencing
nucleoid-associated protein
Lsr2
url https://journals.asm.org/doi/10.1128/mBio.01077-21
work_keys_str_mv AT xiafeizhang interplaybetweennucleoidassociatedproteinsandtranscriptionfactorsincontrollingspecializedmetabolisminitalictoggleyesstreptomycesitalic
AT saranandres interplaybetweennucleoidassociatedproteinsandtranscriptionfactorsincontrollingspecializedmetabolisminitalictoggleyesstreptomycesitalic
AT marieaelliot interplaybetweennucleoidassociatedproteinsandtranscriptionfactorsincontrollingspecializedmetabolisminitalictoggleyesstreptomycesitalic