Evidence map›Paper›PMID 33325950›Full record

ArticleMetallomics : integrated biometal science2020

Differential translational control of 5' IRE-containing mRNA in response to dietary iron deficiency and acute iron overload.

Kerry R Garza, Stephen L Clarke, Yi-Hsuan Ho, Matthew D Bruss, Aparna Vasanthakumar, Sheila A Anderson, Richard S Eisenstein

Open access · hybridAbstract read
In one paragraph

Article in Metallomics : integrated biometal science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
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  5. Article
  6. Article
  7. Review
  8. Article
  9. Elucidating Iron Metabolism through Molecular Imaging.Current issues in molecular biology · 2024
    Review
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  11. Article
  12. Article
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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 1 institution in 1 country.

Kerry R GarzaUniversity of Wisconsin-Madison, Department of Nutritional Sciences, 1415 Linden Drive, Madison, WI 53706, USA. eisenste@nutrisci.wisc.edu.
Stephen L Clarke
Yi-Hsuan Ho
Matthew D Bruss
Aparna Vasanthakumar
Sheila A Anderson
Richard S Eisenstein
University of Wisconsin–Madison · US

Funding

TRAINING IN NUTRITIONT32DK007665 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI GUY E GROBLEWSKI, Chi- Liang Eric Yen · 1993 to 2026
$9.2M
Biological Functions of Iron Responsive ElementsR01DK066600 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI EISENSTEIN, RICHARD S. · 2005 to 2017
$3.4M
NIDDK NIH HHS R01 DK066600NIDDK NIH HHS T32 DK007665
6 · The paper itself

Abstract

Iron regulatory proteins (IRPs) are iron-responsive RNA binding proteins that dictate changes in cellular iron metabolism in animal cells by controlling the fate of mRNAs containing iron responsive elements (IREs). IRPs have broader physiological roles as some targeted mRNAs encode proteins with functions beyond iron metabolism suggesting hierarchical regulation of IRP-targeted mRNAs. We observe that the translational regulation of IRP-targeted mRNAs encoding iron storage (L- and H-ferritins) and export (ferroportin) proteins have different set-points of iron responsiveness compared to that for the TCA cycle enzyme mitochondrial aconitase. The ferritins and ferroportin mRNA were largely translationally repressed in the liver of rats fed a normal diet whereas mitochondrial aconitase mRNA is primarily polysome bound. Consequently, acute iron overload increases polysome association of H- and L-ferritin and ferroportin mRNAs while mitochondrial aconitase mRNA showed little stimulation. Conversely, mitochondrial aconitase mRNA is most responsive in iron deficiency. These differences in regulation were associated with a faster off-rate of IRP1 for the IRE of mitochondrial aconitase in comparison to that of L-ferritin. Thus, hierarchical control of mRNA translation by IRPs involves selective control of cellular functions acting at different states of cellular iron status and that are critical for adaptations to iron deficiency or prevention of iron toxicity.

Indexed as

Anemia, Iron-DeficiencyAnimalsCation Transport ProteinsFerritinsFerroportinIron OverloadIron-Regulatory ProteinsMaleMiceProtein BiosynthesisRats, Sprague-DawleyRNA, MessengerCation Transport ProteinsFerritinsFerroportinIron-Regulatory ProteinsRNA, Messenger

Identifiers

PMID33325950
PMCPMC8057200
OpenAlexW3117563817

What OpenQuestion holds

Textmetadata
LicenceTDM
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.