Evidence map›Paper›PMID 38725184›Full record

ArticleMolecular microbiology2024

Bradyrhizobium japonicum HmuP is an RNA-binding protein that positively controls hmuR operon expression by suppression of a negative regulatory RNA element in the 5' untranslated region.

Peipei Wu, Alasteir Ong, Mark R O'Brian

Abstract read
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Article in Molecular microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Peipei WuDepartment of Biochemistry, Jacobs School of Medicine and Biomedical Sciences, The University at Buffalo, Buffalo, New York, USA.
Alasteir OngDepartment of Biochemistry, Jacobs School of Medicine and Biomedical Sciences, The University at Buffalo, Buffalo, New York, USA.
Mark R O'BrianDepartment of Biochemistry, Jacobs School of Medicine and Biomedical Sciences, The University at Buffalo, Buffalo, New York, USA.ORCID 0000-0001-5196-7594

Funding

Bacterial adaptation to iron stressR01GM122947 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI O'BRIAN, MARK R · 2017 to 2020
$1.3M
NIGMS NIH HHS R01 GM122947
6 · The paper itself

Abstract

The hmuR operon encodes proteins for the uptake and utilization of heme as a nutritional iron source in Bradyrhizobium japonicum. The hmuR operon is transcriptionally activated by the Irr protein and is also positively controlled by HmuP by an unknown mechanism. An hmuP mutant does not express the hmuR operon genes nor does it grow on heme. Here, we show that hmuR expression from a heterologous promoter still requires hmuP, suggesting that HmuP does not regulate at the transcriptional level. Replacement of the 5' untranslated region (5'UTR) of an HmuP-independent gene with the hmuR 5'UTR conferred HmuP-dependent expression on that gene. Recombinant HmuP bound an HmuP-responsive RNA element (HPRE) within the hmuR 5'UTR. A 2 nt substitution predicted to destabilize the secondary structure of the HPRE abolished both HmuP binding activity in vitro and hmuR expression in cells. However, deletion of the HPRE partially restored hmuR expression in an hmuP mutant, and it rescued growth of the hmuP mutant on heme. These findings suggest that the HPRE is a negative regulatory RNA element that is suppressed when bound by HmuP to express the hmuR operon.

Indexed as

5' Untranslated RegionsBacterial ProteinsBradyrhizobiumGene Expression Regulation, BacterialOperonRNA-Binding ProteinsHemePromoter Regions, GeneticProtein BindingRNA, Bacterial5' Untranslated RegionsBacterial ProteinsHemeRNA, BacterialRNA-Binding Proteinsbacterial gene expressionheme transportiron acquisitionpost‐transcriptional regulationRNA binding protein

Identifiers

PMID38725184
PMCPMC11176003

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.