Evidence map›Paper›PMID 19924247›Full record

ArticlePloS one2009

SMF-1, SMF-2 and SMF-3 DMT1 orthologues regulate and are regulated differentially by manganese levels in C. elegans.

Catherine Au, Alexandre Benedetto, Joel Anderson, Arnaud Labrousse, Keith Erikson, Jonathan J Ewbank, Michael Aschner

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

57 citing papers in PubMed, 97 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Cecytb-2, a CytochromeBiomolecules · 2025
    Article
  6. International journal of molecular sciences · 2025
    Article
  7. Article
  8. Review
  9. Consequences of Disturbing Manganese Homeostasis.International journal of molecular sciences · 2023
    Review
  10. Article
  11. Biomolecules · 2022
    Review
  12. Manganese-Induced Toxicity inInternational journal of molecular sciences · 2022
    Article
  13. Review
  14. Article
  15. Xenobiotic metabolism and transport inJournal of toxicology and environmental health. Part B, Critical reviews · 2021
    Review
  16. The impact of manganese on neurotransmitter systems.Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS) · 2020
    Review
  17. Article
  18. Article
  19. Identification of Toxicity Effects of CuEnvironmental science. Nano · 2020
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 6 institutions in 3 countries.

Catherine AuDepartment of Pediatrics, Vanderbilt University, Nashville, Tennessee, USA.
Alexandre Benedetto
Joel Anderson
Arnaud Labrousse
Keith Erikson
Jonathan J Ewbank
Michael Aschner
University of North Carolina at Greensboro · USCentre National de la Recherche Scientifique · FRInserm · FRMonroe Carell Jr. Children's Hospital · USUniversity College London · GBVanderbilt University · US

Funding

Mechanisms of Manganese NeurotoxicityR01ES010563 · NIEHS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Michael Aschner, Aaron B Bowman · 2001 to 2026
$11.9M
NIEHS NIH HHS R01 ES010563NIEHS NIH HHS R01 ES10563NINDS NIH HHS R15 NS
6 · The paper itself

Abstract

Manganese (Mn) is an essential metal that can exert toxic effects at high concentrations, eventually leading to Parkinsonism. A major transporter of Mn in mammals is the divalent-metal transporter (DMT1). We characterize here DMT1-like proteins in the nematode C. elegans, which regulate and are regulated by Mn and iron (Fe) content. We identified three new DMT1-like genes in C. elegans: smf-1, smf-2 and smf-3. All three can functionally substitute for loss of their yeast orthologues in S. cerevisiae. In the worm, deletion of smf-1 or smf-3 led to an increased Mn tolerance, while loss of smf-2 led to increased Mn sensitivity. smf mRNA levels measured by QRT-PCR were up-regulated upon low Mn and down-regulated upon high Mn exposures. Translational GFP-fusions revealed that SMF-1 and SMF-3 strongly localize to partially overlapping apical regions of the gut epithelium, suggesting a differential role for SMF-1 and SMF-3 in Mn nutritional intake. Conversely, SMF-2 was detected in the marginal pharyngeal epithelium, possibly involved in metal-sensing. Analysis of metal content upon Mn exposure in smf mutants revealed that SMF-3 is required for normal Mn uptake, while smf-1 was dispensable. Higher smf-2 mRNA levels correlated with higher Fe content, supporting a role for SMF-2 in Fe uptake. In smf-1 and smf-3 but not in smf-2 mutants, increased Mn exposure led to decreased Fe levels, suggesting that both metals compete for transport by SMF-2. Finally, SMF-3 was post-translationally and reversibly down-regulated following Mn-exposure. In sum, we unraveled a complex interplay of transcriptional and post-translational regulations of 3 DMT1-like transporters in two adjacent tissues, which regulate metal-content in C. elegans.

Indexed as

Gene Expression RegulationAmino Acid SequenceAnimalsAnimals, Genetically ModifiedBiological TransportCaenorhabditis elegansCaenorhabditis elegans ProteinsCation Transport ProteinsCloning, MolecularGene DeletionIronManganeseMetalsMolecular Sequence DataSaccharomyces cerevisiaeSequence Homology, Amino AcidCaenorhabditis elegans ProteinsCation Transport ProteinsIronManganeseMetalssmf-1 protein, C eleganssmf-2 protein, C eleganssmf-3 protein, C elegansSolute Carrier Family 11, Member 2

Identifiers

PMID19924247
PMCPMC2773845
OpenAlexW2165246198

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.