TroR is the primary regulator of the iron homeostasis transcription network in the halophilic archaeon Haloferax volcanii

Author:

Martinez Pastor Mar1,Sakrikar Saaz2,Hwang Sungmin3,Hackley Rylee K14,Soborowski Andrew L15,Maupin-Furlow Julie A67ORCID,Schmid Amy K1458ORCID

Affiliation:

1. Department of Biology, Duke University , Durham , NC  27708 , USA

2. Center for Genomics and System Biology at NYU Department of Biology, New York University , NY , NY  10003 , USA

3. Division of Practical Research, Honam National Institute of Biological Resources , Jeollanam-do , Mokpo-si  58762 , Republic of Korea

4. University Program in Genetics and Genomics, Duke University , Durham , NC  27708,  USA

5. Computational Biology and Bioinformatics graduate program, Duke University , Durham , NC  27708,  USA

6. Department of Microbiology and Cell Science, Institute of Food and Agricultural Sciences, University of Florida , Gainesville , FL  32611,  USA

7. Genetics Institute, University of Florida , Gainesville , FL  32611,  USA

8. Center for Genomics and Computational Biology, Duke University , Durham , NC  27708,  USA

Abstract

Abstract Maintaining the intracellular iron concentration within the homeostatic range is vital to meet cellular metabolic needs and reduce oxidative stress. Previous research revealed that the haloarchaeon Halobacterium salinarum encodes four diphtheria toxin repressor (DtxR) family transcription factors (TFs) that together regulate the iron response through an interconnected transcriptional regulatory network (TRN). However, the conservation of the TRN and the metal specificity of DtxR TFs remained poorly understood. Here we identified and characterized the TRN of Haloferax volcanii for comparison. Genetic analysis demonstrated that Hfx. volcanii relies on three DtxR transcriptional regulators (Idr, SirR, and TroR), with TroR as the primary regulator of iron homeostasis. Bioinformatics and molecular approaches revealed that TroR binds a conserved cis-regulatory motif located ∼100 nt upstream of the start codon of iron-related target genes. Transcriptomics analysis demonstrated that, under conditions of iron sufficiency, TroR repressed iron uptake and induced iron storage mechanisms. TroR repressed the expression of one other DtxR TF, Idr. This reduced DtxR TRN complexity relative to that of Hbt. salinarum appeared correlated with natural variations in iron availability. Based on these data, we hypothesize that variable environmental conditions such as iron availability appear to select for increasing TRN complexity.

Funder

National Science Foundation

U.S. Department of Energy

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Genetics

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