Evidence map›Paper›PMID 29979728›Full record

ArticlePloS one2018

Rv1460, a SufR homologue, is a repressor of the suf operon in Mycobacterium tuberculosis.

Danicke Willemse, Brandon Weber, Laura Masino, Robin M Warren, Salvatore Adinolfi, Annalisa Pastore, Monique J Williams

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.5field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 38 citations in OpenAlex.

  1. Recent Characterization of Key Proteins to Combat Tuberculosis.Advances in experimental medicine and biology · 2026
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  6. Multiple factors regulate the expression ofFrontiers in cellular and infection microbiology · 2024
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  7. TheMicroorganisms · 2023
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  15. Review
  16. Article
  17. Discovery of a Natural Product That Binds to theMolecules (Basel, Switzerland) · 2020
    Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 6 institutions in 3 countries.

Danicke WillemseDST-NRF Centre of Excellence for Biomedical Tuberculosis Research; South African Medical Research Council Centre for Tuberculosis Research; Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.
Brandon WeberElectron Microscope Unit, University of Cape Town, Cape Town, South Africa.
Laura MasinoStructural Biology Science Technology Platform, The Francis Crick Institute, London, United Kingdom.
Robin M WarrenDST-NRF Centre of Excellence for Biomedical Tuberculosis Research; South African Medical Research Council Centre for Tuberculosis Research; Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.
Salvatore AdinolfiPharmaceutical Science and Technology, University of Turin, Turin, Italy.
Annalisa PastoreDepartment of Basic and Clinical Neuroscience, Maurice Wohl Institute, King's College London, London, United Kingdom.
Monique J WilliamsDST-NRF Centre of Excellence for Biomedical Tuberculosis Research; South African Medical Research Council Centre for Tuberculosis Research; Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa.
South African Medical Research Council · ZAKing's College London · GBStellenbosch University · ZAThe Francis Crick Institute · GBUniversity of Cape Town · ZAUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Iron-sulphur (Fe-S) clusters are ubiquitous co-factors which require multi-protein systems for their synthesis. In Mycobacterium tuberculosis, the Rv1460-Rv1461-Rv1462-Rv1463-csd-Rv1465-Rv1466 operon (suf operon) encodes the primary Fe-S cluster biogenesis system. The first gene in this operon, Rv1460, shares homology with the cyanobacterial SufR, which functions as a transcriptional repressor of the sufBCDS operon. Rv1460's function in M. tuberculosis has however not been determined. In this study, we demonstrate that M. tuberculosis mutants lacking a functional Rv1460 protein are impaired for growth under standard culture conditions. Elevated expression of Rv1460 and Rv1461 was observed in the mutant, implicating Rv1460 in the regulation of the suf operon. Binding of an Fe-S cluster to purified recombinant Rv1460 was confirmed by UV-visible spectroscopy and circular dichroism. Furthermore, three conserved cysteine residues, C203, C216 and C244, proposed to provide ligands for the coordination of an Fe-S cluster, were shown to be required for the function of Rv1460 in M. tuberculosis. Rv1460 therefore seems to be functionally analogous to cyanobacterial SufR.

Indexed as

Genes, BacterialAmino Acid SequenceBacterial ProteinsBinding SitesConserved SequenceCyanobacteriaGene DeletionHumansIron-Sulfur ProteinsMutationMycobacterium tuberculosisOperonPromoter Regions, GeneticRecombinant ProteinsRepressor ProteinsBacterial ProteinsIron-Sulfur ProteinsRecombinant ProteinsRepressor Proteins

Identifiers

PMID29979728
PMCPMC6034842
OpenAlexW2845745072

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.