Evidence map›Paper›PMID 22427968›Full record

ArticlePloS one2012

Two isoforms of the mRNA binding protein IGF2BP2 are generated by alternative translational initiation.

Hang T T Le, Alice M Sorrell, Kenneth Siddle

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. 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
1.6field-weighted citation impact, top 17% 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, 25 citations in OpenAlex.

  1. Article
  2. Impact ofInternational journal of medical sciences · 2026
    Article
  3. Article
  4. Review
  5. The Characterization and Differential Analysis of mAnimals : an open access journal from MDPI · 2023
    Article
  6. IGF2BP2 promotes cancer progression by degrading the RNA transcript encoding a v-ATPase subunit.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. RNA-binding proteins impacting on internal initiation of translation.International journal of molecular sciences · 2013
    Review
  12. Genetics of type 2 diabetes.World journal of diabetes · 2013
    Article
  13. Review
  14. Article
  15. Article
  16. 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

3 authors at 2 institutions in 2 countries.

Hang T T LeUniversity of Cambridge Metabolic Research Laboratories and Department of Clinical Biochemistry, Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, United Kingdom.
Alice M Sorrell
Kenneth Siddle
Addenbrooke's Hospital · GBUniversity of Cambridge · GB

Funding

Medical Research Council G0600717
6 · The paper itself

Abstract

IGF2BP2 is a member of a family of mRNA binding proteins that, collectively, have been shown to bind to several different mRNAs in mammalian cells, including one of the mRNAs encoding insulin-like growth factor-2. Polymorphisms in the Igf2bp2 gene are associated with risk of developing type 2 diabetes, but detailed functional characterisation of IGF2BP2 protein is lacking. By immunoblotting with C-terminally reactive antibodies we identified a novel IGF2BP2 isoform with a molecular weight of 58 kDa in both human and rodents, that is expressed at somewhat lower levels than the full-length 65 kDa protein. We demonstrated by mutagenesis that this isoform is generated by alternative translation initiation at the internal Met69. It lacks a conserved N-terminal RNA Recognition Motif (RRM) and would be predicted to differ functionally from the canonical full length isoform. We further investigated IGF2BP2 mRNA transcripts by amplification of cDNA using 5'-RACE. We identified multiple transcription start sites of the human, mouse and rat Igf2bp2 genes in a highly conserved region only 50-90 nts upstream of the major translation start site, ruling out the existence of N-terminally extended isoforms. We conclude that structural heterogeneity of IGF2BP2 protein should be taken into account when considering cellular function.

Indexed as

Amino Acid SequenceAnimalsBlotting, WesternDNA, ComplementaryHumansMiceMolecular Sequence DataMutagenesisPeptide Chain Initiation, TranslationalProtein IsoformsRatsRNA-Binding ProteinsSequence Analysis, DNASpecies SpecificityTranscription Initiation SiteDNA, ComplementaryIGF2BP2 protein, humanIGF2BP2 protein, mouseProtein IsoformsRNA-Binding Proteins

Identifiers

PMID22427968
PMCPMC3299737
OpenAlexW2053135283

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.