Affiliation:
1. TB Center, The Public Health Research Institute, Newark, New Jersey 07103
2. Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California 94305
3. Department of Microbiology, New York University Medical Center, New York, New York 10016
Abstract
ABSTRACT
The mycobacterial IdeR protein is a metal-dependent regulator of the DtxR (diphtheria toxin repressor) family. In the presence of iron, it binds to a specific DNA sequence in the promoter regions of the genes that it regulates, thus controlling their transcription. In this study, we provide evidence that
ideR
is an essential gene in
Mycobacterium tuberculosis. ideR
cannot normally be disrupted in this mycobacterium in the absence of a second functional copy of the gene. However, a rare
ideR
mutant was obtained in which the lethal effects of
ideR
inactivation were alleviated by a second-site suppressor mutation and which exhibited restricted iron assimilation capacity. Studies of this strain and a derivative in which IdeR expression was restored allowed us to identify phenotypic effects resulting from
ideR
inactivation. Using DNA microarrays, the iron-dependent transcriptional profiles of the wild-type,
ideR
mutant, and
ideR
-complemented mutant strains were analyzed, and the genes regulated by iron and IdeR were identified. These genes encode a variety of proteins, including putative transporters, proteins involved in siderophore synthesis and iron storage, members of the PE/PPE family, a membrane protein involved in virulence, transcriptional regulators, and enzymes involved in lipid metabolism.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
431 articles.
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