Evidence map›Paper›PMID 34252531›Full record

ReviewGene2021

A role for zinc transporter gene SLC39A12 in the nervous system and beyond.

Danielle N Davis, Morgan D Strong, Emily Chambers, Matthew D Hart, Ahmed Bettaieb, Stephen L Clarke, Brenda J Smith, Barbara J Stoecker, Edralin A Lucas, Dingbo Lin and 1 more

Open access · greenAbstract readReview
In one paragraph

Review in Gene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

19 citing papers in PubMed, 18 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Danielle N DavisOklahoma State University, Department of Nutritional Sciences, Stillwater, OK 74078, USA.
Morgan D StrongOklahoma State University, Department of Nutritional Sciences, Stillwater, OK 74078, USA.
Emily ChambersOklahoma State University, Department of Nutritional Sciences, Stillwater, OK 74078, USA.
Matthew D HartOklahoma State University, Department of Nutritional Sciences, Stillwater, OK 74078, USA.
Ahmed BettaiebUniversity of Tennessee, Department of Nutrition, Knoxville, TN 37996, USA.
Stephen L ClarkeOklahoma State University, Department of Nutritional Sciences, Stillwater, OK 74078, USA.
Brenda J SmithOklahoma State University, Department of Nutritional Sciences, Stillwater, OK 74078, USA.
Barbara J StoeckerOklahoma State University, Department of Nutritional Sciences, Stillwater, OK 74078, USA.
Edralin A LucasOklahoma State University, Department of Nutritional Sciences, Stillwater, OK 74078, USA.
Dingbo LinOklahoma State University, Department of Nutritional Sciences, Stillwater, OK 74078, USA.
Winyoo ChowanadisaiOklahoma State University, Department of Nutritional Sciences, Stillwater, OK 74078, USA. Electronic address: winyoo.chowanadisai@okstate.edu.
Oklahoma State University · USUniversity of Tennessee at Knoxville · US

Funding

The Gene Wiki: Community intelligence applied to gene annotationR01GM089820 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI SU, ANDREW I · 2010 to 2021
$5.2M
NIGMS NIH HHS R01 GM089820
6 · The paper itself

Abstract

The SLC39A12 gene encodes the zinc transporter protein ZIP12, which is expressed across many tissues and is highly abundant in the vertebrate nervous system. As a zinc transporter, ZIP12 functions to transport zinc across cellular membranes, including cellular zinc influx across the plasma membrane. Genome-wide association and exome sequencing studies have shown that brain susceptibility-weighted magnetic resonance imaging (MRI) intensity is associated with ZIP12 polymorphisms and rare mutations. ZIP12 is required for neural tube closure and embryonic development in Xenopus tropicalis. Frog embryos depleted of ZIP12 by antisense morpholinos develop an anterior neural tube defect and lack viability. ZIP12 is also necessary for neurite outgrowth and mitochondrial function in mouse neural cells. ZIP12 mRNA is increased in brain regions of schizophrenic patients. Outside of the nervous system, hypoxia induces ZIP12 expression in multiple mammalian species, including humans, which leads to endothelial and smooth muscle thickening in the lung and contributes towards pulmonary hypertension. Other studies have associated ZIP12 with other diseases such as cancer. Given that ZIP12 is highly expressed in the brain and that susceptibility-weighted MRI is associated with brain metal content, ZIP12 may affect neurological diseases and psychiatric illnesses such as Parkinson's disease, Alzheimer's disease, and schizophrenia. Furthermore, the induction of ZIP12 and resultant zinc uptake under pathophysiological conditions may be a critical component of disease pathology, such as in pulmonary hypertension. Drug compounds that bind metals like zinc may be able to treat diseases associated with impaired zinc homeostasis and altered ZIP12 function.

Indexed as

Nervous System Physiological PhenomenaAnimalsAutistic DisorderBiological Specimen BanksCation Transport ProteinsGene Expression Regulation, DevelopmentalHumansLungMultigene FamilyNeurodegenerative DiseasesOxidative StressUnited KingdomVertebratesXenopus ProteinsZincCation Transport ProteinsSLC39A12 protein, humanslc39a12 protein, XenopusXenopus ProteinsZincBrainGeneticsLungMetalMRIZIP12

Identifiers

PMID34252531
PMCPMC8318780
OpenAlexW3178136366

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.