Evidence map›Paper›PMID 18020946›Full record

ArticleBiological chemistry2007

Novel zinc-responsive post-transcriptional mechanisms reciprocally regulate expression of the mouse Slc39a4 and Slc39a5 zinc transporters (Zip4 and Zip5).

Benjamin P Weaver, Jodi Dufner-Beattie, Taiho Kambe, Glen K Andrews

Abstract read
In one paragraph

Article in Biological chemistry, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 4% 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

71 citing papers in PubMed, 1 synthesis or guideline pooled it, 160 citations in OpenAlex.

  1. Pooled it
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  9. Role of zinc in health and disease.Clinical and experimental medicine · 2024
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  12. The Molecular Basis for Zinc Bioavailability.International journal of molecular sciences · 2023
    Review
  13. Analysis of the Association of Two SNPs in the Promoter Regions of theAnimals : an open access journal from MDPI · 2022
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  18. Enhancing effect ofJournal of ginseng research · 2022
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11 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

Benjamin P WeaverDepartment of Biochemistry and Molecular Biology, University of Kansas Medical Center, Kansas City, KS 66160-7421, USA. gandrews@kumc.edu
Jodi Dufner-Beattie
Taiho Kambe
Glen K Andrews
University of Kansas Medical Center · US

Funding

A Mouse Model of Acrodermatitis EnteropathicaR01DK063975 · NIDDK · UNIVERSITY OF KANSAS MEDICAL CENTER · PI ANDREWS, GLEN K · 2003 to 2012
$3.1M
NIDDK NIH HHS DK063975NIDDK NIH HHS R01 DK063975
6 · The paper itself

Abstract

Dietary zinc deficiency in mice is accompanied by enhanced expression of the zinc uptake transporter Slc39a4 (Zip4) and repressed expression of Slc39a5 (Zip5) in tissues which regulate zinc homeostasis (intestine, pancreas and visceral yolk sac). Herein, mechanisms controlling this differential expression were investigated. The induction of Zip4 mRNA during zinc deficiency, and its repression in response to zinc repletion were found to reflect changes in Zip4 mRNA stability and not changes in the relative rate of transcription of this gene. During zinc deficiency, ZIP4 protein levels are increased and this protein is localized on the apical membranes. Administration of an oral gavage of zinc caused ZIP4 internalization and degradation in enterocytes and visceral endoderm cells. Similarly, ZIP4 is induced by zinc deficiency in cultured mouse Hepa cells and is rapidly degraded in response to added zinc. Zip5 mRNA abundance does not change in response to zinc, but the translation of this mRNA was found to be zinc-responsive. During zinc deficiency, Zip5 mRNA remains associated with polysomes, while the protein is internalized and degraded in enterocytes, acinar cells and endoderm cells. After zinc-gavage, ZIP5 is rapidly resynthesized and targeted to the basolateral membranes of these cell types.

Indexed as

AnimalsBlotting, NorthernBlotting, WesternCation Transport ProteinsCell LineCentrifugation, Density GradientDietFemaleGene Expression RegulationImmunohistochemistryImmunoprecipitationKineticsMembrane ProteinsMiceOrgan Culture TechniquesPolyribosomesCation Transport ProteinsMembrane ProteinsRNA, MessengerSlc39a4 protein, mouseSlc39a5 protein, mouseZinc

Identifiers

PMID18020946
PMCPMC2376820
OpenAlexW2090003468

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.