Evidence map›Paper›PMID 23298867›Full record

ArticleChemico-biological interactions2013

Alternative splicing in the aldo-keto reductase superfamily: implications for protein nomenclature.

Oleg A Barski, Rebekka Mindnich, Trevor M Penning

Abstract read
In one paragraph

Article in Chemico-biological interactions, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. The aldo-keto reductases (AKRs): Overview.Chemico-biological interactions · 2015
    Review
  4. Article
  5. Review
  6. Review
  7. Review
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

3 authors.

Oleg A BarskiDiabetes and Obesity Center, School of Medicine, University of Louisville, Louisville, KY 40202, USA. o.barski@louisville.edu
Rebekka Mindnich
Trevor M Penning

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Susan M Domchek · 1985 to 2026
$222.3M
Translational Research Support CoreP30ES013508 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI Trevor M Penning · 2006 to 2026
$35.3M
STEM CELLS AND DIABETIC CARDIOMYOPATHY PROJ 2 2009P20RR024489 · NCRR · UNIVERSITY OF LOUISVILLE · PI BHATNAGAR, ARUNI · 2008 to 2011
$10.0M
Structure/Function of Steroid Transforming AKR'sR01DK047015 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI PENNING, TREVOR M · 1994 to 2011
$3.2M
Oxidoreductase Activity of the Beta Subunit of Kv ChannelsR21HL089372 · NHLBI · UNIVERSITY OF LOUISVILLE · PI BARSKI, OLEG A · 2008 to 2009
$407k
NCI NIH HHS P30 CA016520NCRR NIH HHS P20 RR024489NCRR NIH HHS RR-24489NHLBI NIH HHS HL-89372NHLBI NIH HHS R21 HL089372NIDDK NIH HHS R01 DK047015NIDDK NIH HHS R01-DK47015NIEHS NIH HHS P30 ES013508NIEHS NIH HHS P30-ES13508
6 · The paper itself

Abstract

The aldo-keto reductase superfamily contains 173 proteins which are present in all phyla. Examination of the human and mouse genomes has identified that in some instances a single AKR gene can give rise to alternatively spliced mRNA variants which in some cases can give rise to more than one protein isoform. This is currently well documented in the AKR6A subfamily which contains the β-subunits of the voltage-gated potassium ion channels. With the emergence of second generation sequencing it is likely that the occurrence of transcript variants and protein isoforms from a single AKR gene may become common place. To deal with this issue we recommend that the Ensembl data-base nomenclature be used to annotate the transcript variants from a single AKR gene. However, since multiple transcript variants could give rise to either the same or multiple protein isoforms from the same AKR gene we also propose to expand the nomenclature of the AKR protein superfamily, so that when a protein isoform is shown to be expressed and is functional it would be assigned the standard AKR name followed by a "period or full-stop" and a number for that unique isoform. Numbers will be assigned chronologically and linked to the respective transcripts annotated in Ensembl e.g. AKR6A5.1 (Kvβ2.1) (AKR6A5-001, -006 and -201), followed by AKR6A5.2 (Kvβ2.2) (AKR6A5-002,-202). This nomenclature is expandable and it enables multiple protein isoforms to be assigned to their respective transcripts when they arise from the same AKR gene or for a single protein isoform to be assigned to multiple transcripts when the transcripts encode the same AKR protein.

Indexed as

Alcohol OxidoreductasesAldehyde ReductaseAldo-Keto ReductasesAlternative SplicingAnimalsHumansIsoenzymesMicePotassium Channels, Voltage-GatedProtein IsoformsRNA, MessengerUntranslated RegionsAKR7A5 protein, mouseAlcohol OxidoreductasesAldehyde ReductaseAldo-Keto ReductasesIsoenzymesPotassium Channels, Voltage-GatedProtein IsoformsRNA, MessengerUntranslated Regions

Identifiers

PMID23298867
PMCPMC3758225

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Registered trials

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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.