Evidence map›Paper›PMID 24798331›Full record

ArticleThe Journal of biological chemistry2014

Expression of the yeast cation diffusion facilitators Mmt1 and Mmt2 affects mitochondrial and cellular iron homeostasis: evidence for mitochondrial iron export.

Liangtao Li, Ren Miao, Xuan Jia, Diane M Ward, Jerry Kaplan

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. Adaptation ofInternational journal of molecular sciences · 2022
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. The mitochondrial iron exporter genesThe Journal of biological chemistry · 2020
    Article
  10. Article
  11. Mitochondrial Iron in Human Health and Disease.Annual review of physiology · 2019
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Mitochondria and Iron: current questions.Expert review of hematology · 2017
    Review
  17. Article
  18. 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

5 authors at 1 institution in 1 country.

Liangtao LiFrom the Department of Pathology, School of Medicine, University of Utah, Salt Lake City, Utah 84132.
Ren MiaoFrom the Department of Pathology, School of Medicine, University of Utah, Salt Lake City, Utah 84132.
Xuan JiaFrom the Department of Pathology, School of Medicine, University of Utah, Salt Lake City, Utah 84132.
Diane M WardFrom the Department of Pathology, School of Medicine, University of Utah, Salt Lake City, Utah 84132.
Jerry KaplanFrom the Department of Pathology, School of Medicine, University of Utah, Salt Lake City, Utah 84132 jerry.kaplan@path.utah.edu.
University of Utah · US

Funding

The Genetic Analysis of Mitochondrial Iron MetabolismR01DK052380 · NIDDK · UNIVERSITY OF UTAH · PI WARD, DIANE MCVEY · 1998 to 2016
$5.6M
FACTORS REGULATING THE CELLULAR UPTAKE OF IRONR01DK030534 · NIDDK · UNIVERSITY OF UTAH · PI WARD, DIANE MCVEY · 1986 to 2018
$2.7M
NIDDK NIH HHS DK035034NIDDK NIH HHS DK052380NIDDK NIH HHS R01 DK030534NIDDK NIH HHS R01 DK052380
6 · The paper itself

Abstract

Mmt1 and Mmt2 are highly homologous yeast members of the cation diffusion facilitator transporter family localized to mitochondria. Overexpression of MMT1/2 led to changes in cellular metal homeostasis (increased iron sensitivity, decreased cobalt sensitivity, increased sensitivity to copper), oxidant generation, and increased sensitivity to H2O2. The phenotypes due to overexpression of MMT1&2 were similar to that seen in cells with deletions in MRS3 and MRS4, genes that encode the mitochondrial iron importers. Overexpression of MMT1&2 resulted in induction of the low iron transcriptional response, similar to that seen in Δmrs3Δmr4 cells. This low iron transcriptional response was suppressed by deletion of CCC1, the gene that encodes the vacuolar iron importer. Measurement of the activity of the iron-dependent gentisate 1,2-dioxygenase from Pseudaminobacter salicylatoxidans expressed in yeast cytosol, showed that changes in Mmt1/2 levels affected cytosol iron concentration even in the absence of Ccc1. Overexpression of MMT1 resulted in increased cytosolic iron whereas deletion of MMT1/MMT2 led to decreased cytosolic iron. These results support the hypothesis that Mmt1/2 function as mitochondrial iron exporters.

Indexed as

Cation Transport ProteinsCytoplasmHomeostasisIon TransportIronMitochondriaMitochondrial ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCation Transport ProteinsCCC1 protein, S cerevisiaeIronMitochondrial ProteinsMMT1 protein, S cerevisiaeMMT2 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsIronMetal HomeostasisMitochondriaOxygen RadicalsTransport Metal

Identifiers

PMID24798331
PMCPMC4059154
OpenAlexW1967140535

What OpenQuestion holds

Textmetadata
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.