Roles of three FurA paralogs in the regulation of genes pertaining to peroxide defense in Mycobacterium smegmatis mc(2)155open access
- Authors
- Lee, Ha-Na; Ji, Chang-Jun; Lee, Hyun-Hee; Park, Jungwook; Seo, Young-Su; Lee, Jin-Won; Oh, Jeong-Il
- Issue Date
- Jun-2018
- Publisher
- WILEY
- Citation
- MOLECULAR MICROBIOLOGY, v.108, no.6, pp.661 - 682
- Indexed
- SCIE
SCOPUS
- Journal Title
- MOLECULAR MICROBIOLOGY
- Volume
- 108
- Number
- 6
- Start Page
- 661
- End Page
- 682
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/16893
- DOI
- 10.1111/mmi.13956
- ISSN
- 0950-382X
- Abstract
- Mycobacterium smegmatis mc(2)155 has three genes (MSMEG_6383, furA1; MSMEG_3460, furA2; MSMEG_6253, furA3) encoding FurA (ferric-uptake regulator A) paralogs. Three FurA paralogs in M. smegmatis are functionally redundant and negatively regulate expression of a subset of genes involved in peroxide detoxification such as ahpC, katG1 and katG2, as well as their own genes. The FurA paralogs sense H2O2 via metal-catalyzed His oxidation (MCHO) in the same way as PerR. The propensity of FurA2 and FurA3 for MCHO is greater than that of FurA1. The three furA genes are transcribed into leaderless mRNAs lacking the Shine-Dalgarno (SD) sequence. FurA1 and FurA3 have the quaternary structure of homodimers like most Fur homologs, whereas FurA2 occurs as a monomer. The monomeric structure of FurA2 is determined by the C-terminal region of its dimerization domain. FurA2 monomers appear to cooperatively bind to the FurA-binding site with an inverted repeat configuration and have a broader binding specificity for the target DNA than dimeric FurA1 and FurA3. Comparative transcriptomic analysis revealed that the FurA paralogs do not regulate genes related to iron homeostasis in M. smegmatis, and that expression of SigF-regulated genes is significantly decreased in a furA triple mutant relative to the wild-type strain of M. smegmatis.
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