Critical Role of Zur and SmtB in Zinc Homeostasis of Mycobacterium smegmatis
Zinc is crucial for many biological processes, as it is an essential cofactor of enzymes and a structural component of regulatory and DNA binding proteins. Hence, all living cells require zinc to maintain constant intracellular levels. However, in excess, zinc is toxic. Therefore, cellular zinc home...
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doaj-f6ec172a30f84371aa40b92ab18cedf02020-11-25T01:22:18ZengAmerican Society for MicrobiologymSystems2379-50772020-04-0152e00880-1910.1128/mSystems.00880-19Critical Role of Zur and SmtB in Zinc Homeostasis of Mycobacterium smegmatisElke GoetheKristin LaarmannJanita LührsMichael JarekJochen MeensAstrid LewinRalph GoetheZinc is crucial for many biological processes, as it is an essential cofactor of enzymes and a structural component of regulatory and DNA binding proteins. Hence, all living cells require zinc to maintain constant intracellular levels. However, in excess, zinc is toxic. Therefore, cellular zinc homeostasis needs to be tightly controlled. In bacteria, this is achieved by transcriptional regulators whose activity is mediated via zinc-dependent conformational changes promoting or preventing their binding to DNA. SmtB and Zur are important antagonistically acting bacterial regulators in mycobacteria. They sense changes in zinc concentrations in the femtomolar range and regulate transcription of genes for zinc acquisition, storage, and export. Here, we analyzed the role of SmtB and Zur in zinc homeostasis in Mycobacterium smegmatis. Our results revealed novel insights into the transcriptional processes of zinc homeostasis in mycobacteria and their regulation.Zinc homeostasis is crucial for bacterial cells, since imbalances affect viability. However, in mycobacteria, knowledge of zinc metabolism is incomplete. Mycobacterium smegmatis (MSMEG) is an environmental, nonpathogenic Mycobacterium that is widely used as a model organism to study mycobacterial metabolism and pathogenicity. How MSMEG maintains zinc homeostasis is largely unknown. SmtB and Zur are important regulators of bacterial zinc metabolism. In mycobacteria, these regulators are encoded by an operon, whereas in other bacterial species, SmtB and Zur are encoded on separate loci. Here, we show that the smtB-zur operon is consistently present within the genus Mycobacterium but otherwise found only in Nocardia, Saccharothrix, and Corynebacterium diphtheriae. By RNA deep sequencing, we determined the Zur and SmtB regulons of MSMEG and compared them with transcriptional responses after zinc starvation or excess. We found an exceptional genomic clustering of genes whose expression was strongly induced by zur deletion and zinc starvation. These genes encoded zinc importers such as ZnuABC and three additional putative zinc transporters, including the porin MspD, as well as alternative ribosomal proteins. In contrast, only a few genes were affected by deletion of smtB and zinc excess. The zinc exporter ZitA was most prominently regulated by SmtB. Moreover, transcriptional analyses in combination with promoter and chromatin immunoprecipitation assays revealed a special regulation of the smtB-zur operon itself: an apparently zinc-independent, constitutive expression of smtB-zur resulted from sensitive coregulation by both SmtB and Zur. Overall, our data revealed yet unknown peculiarities of mycobacterial zinc homeostasis.https://doi.org/10.1128/mSystems.00880-19zinc homeostasiszinc transporterzinc starvationzinc excesszur regulonsmtb regulonzinc regulationzitazinc importzinc exporttranscriptomicsmycobacteriaznuabcalternative ribosomal proteinschromatin immunoprecipitationcoregulationexportimport |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Elke Goethe Kristin Laarmann Janita Lührs Michael Jarek Jochen Meens Astrid Lewin Ralph Goethe |
spellingShingle |
Elke Goethe Kristin Laarmann Janita Lührs Michael Jarek Jochen Meens Astrid Lewin Ralph Goethe Critical Role of Zur and SmtB in Zinc Homeostasis of Mycobacterium smegmatis mSystems zinc homeostasis zinc transporter zinc starvation zinc excess zur regulon smtb regulon zinc regulation zita zinc import zinc export transcriptomics mycobacteria znuabc alternative ribosomal proteins chromatin immunoprecipitation coregulation export import |
author_facet |
Elke Goethe Kristin Laarmann Janita Lührs Michael Jarek Jochen Meens Astrid Lewin Ralph Goethe |
author_sort |
Elke Goethe |
title |
Critical Role of Zur and SmtB in Zinc Homeostasis of Mycobacterium smegmatis |
title_short |
Critical Role of Zur and SmtB in Zinc Homeostasis of Mycobacterium smegmatis |
title_full |
Critical Role of Zur and SmtB in Zinc Homeostasis of Mycobacterium smegmatis |
title_fullStr |
Critical Role of Zur and SmtB in Zinc Homeostasis of Mycobacterium smegmatis |
title_full_unstemmed |
Critical Role of Zur and SmtB in Zinc Homeostasis of Mycobacterium smegmatis |
title_sort |
critical role of zur and smtb in zinc homeostasis of mycobacterium smegmatis |
publisher |
American Society for Microbiology |
series |
mSystems |
issn |
2379-5077 |
publishDate |
2020-04-01 |
description |
Zinc is crucial for many biological processes, as it is an essential cofactor of enzymes and a structural component of regulatory and DNA binding proteins. Hence, all living cells require zinc to maintain constant intracellular levels. However, in excess, zinc is toxic. Therefore, cellular zinc homeostasis needs to be tightly controlled. In bacteria, this is achieved by transcriptional regulators whose activity is mediated via zinc-dependent conformational changes promoting or preventing their binding to DNA. SmtB and Zur are important antagonistically acting bacterial regulators in mycobacteria. They sense changes in zinc concentrations in the femtomolar range and regulate transcription of genes for zinc acquisition, storage, and export. Here, we analyzed the role of SmtB and Zur in zinc homeostasis in Mycobacterium smegmatis. Our results revealed novel insights into the transcriptional processes of zinc homeostasis in mycobacteria and their regulation.Zinc homeostasis is crucial for bacterial cells, since imbalances affect viability. However, in mycobacteria, knowledge of zinc metabolism is incomplete. Mycobacterium smegmatis (MSMEG) is an environmental, nonpathogenic Mycobacterium that is widely used as a model organism to study mycobacterial metabolism and pathogenicity. How MSMEG maintains zinc homeostasis is largely unknown. SmtB and Zur are important regulators of bacterial zinc metabolism. In mycobacteria, these regulators are encoded by an operon, whereas in other bacterial species, SmtB and Zur are encoded on separate loci. Here, we show that the smtB-zur operon is consistently present within the genus Mycobacterium but otherwise found only in Nocardia, Saccharothrix, and Corynebacterium diphtheriae. By RNA deep sequencing, we determined the Zur and SmtB regulons of MSMEG and compared them with transcriptional responses after zinc starvation or excess. We found an exceptional genomic clustering of genes whose expression was strongly induced by zur deletion and zinc starvation. These genes encoded zinc importers such as ZnuABC and three additional putative zinc transporters, including the porin MspD, as well as alternative ribosomal proteins. In contrast, only a few genes were affected by deletion of smtB and zinc excess. The zinc exporter ZitA was most prominently regulated by SmtB. Moreover, transcriptional analyses in combination with promoter and chromatin immunoprecipitation assays revealed a special regulation of the smtB-zur operon itself: an apparently zinc-independent, constitutive expression of smtB-zur resulted from sensitive coregulation by both SmtB and Zur. Overall, our data revealed yet unknown peculiarities of mycobacterial zinc homeostasis. |
topic |
zinc homeostasis zinc transporter zinc starvation zinc excess zur regulon smtb regulon zinc regulation zita zinc import zinc export transcriptomics mycobacteria znuabc alternative ribosomal proteins chromatin immunoprecipitation coregulation export import |
url |
https://doi.org/10.1128/mSystems.00880-19 |
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