Evidence map›Paper›PMID 17372197›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

The implications of alternative splicing in the ENCODE protein complement.

Michael L Tress, Pier Luigi Martelli, Adam Frankish, Gabrielle A Reeves, Jan Jaap Wesselink, Corin Yeats, Páll Isólfur Olason, Mario Albrecht, Hedi Hegyi, Alejandro Giorgetti and 36 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 126 papers.

0numbers the graph read from it
0cells of the map it votes in
126citing papers in PubMed
12.7field-weighted citation impact, top 1% 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

126 citing papers in PubMed, 220 citations in OpenAlex.

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  9. The genome and transcriptome of the snailbioRxiv : the preprint server for biology · 2023
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66 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

46 authors at 15 institutions in 7 countries.

Michael L TressStructural Computational Biology Programme, Spanish National Cancer Research Centre, E-28029 Madrid, Spain. mtress@cnio.es
Pier Luigi Martelli
Adam Frankish
Gabrielle A Reeves
Jan Jaap Wesselink
Corin Yeats
Páll Isólfur Olason
Mario Albrecht
Hedi Hegyi
Alejandro Giorgetti
Domenico Raimondo
Julien Lagarde
Roman A Laskowski
Gonzalo López
Michael I Sadowski
James D Watson
Piero Fariselli
Ivan Rossi
Alinda Nagy
Wang Kai
Zenia Størling
Massimiliano Orsini
Yassen Assenov
Hagen Blankenburg
Carola Huthmacher
Fidel Ramírez
Andreas Schlicker
France Denoeud
Phil Jones
Samuel Kerrien
Sandra Orchard
Stylianos E Antonarakis
Alexandre Reymond
Ewan Birney
Søren Brunak
Rita Casadio
Roderic Guigo
Jennifer Harrow
Henning Hermjakob
David T Jones
Thomas Lengauer
Christine A Orengo
László Patthy
Janet M Thornton
Anna Tramontano
Alfonso Valencia
European Bioinformatics Institute · GBMax Planck Institute for Informatics · DEUniversity of Bologna · ITHungarian Academy of Sciences · HUInstituto de Salud Carlos III · ESMunicipal Institute for Medical Research · ESMax Planck Society · DESapienza University of Rome · ITUCL Australia · AUUniversity College London · GBWellcome Sanger Institute · GBCenter for Advanced Studies Research and Development in Sardinia · ITSpanish National Cancer Research Centre · ESUniversity of Geneva · CHUniversity of Lausanne · CH

Funding

Wellcome Trust 062023Wellcome Trust 077198
6 · The paper itself

Abstract

Alternative premessenger RNA splicing enables genes to generate more than one gene product. Splicing events that occur within protein coding regions have the potential to alter the biological function of the expressed protein and even to create new protein functions. Alternative splicing has been suggested as one explanation for the discrepancy between the number of human genes and functional complexity. Here, we carry out a detailed study of the alternatively spliced gene products annotated in the ENCODE pilot project. We find that alternative splicing in human genes is more frequent than has commonly been suggested, and we demonstrate that many of the potential alternative gene products will have markedly different structure and function from their constitutively spliced counterparts. For the vast majority of these alternative isoforms, little evidence exists to suggest they have a role as functional proteins, and it seems unlikely that the spectrum of conventional enzymatic or structural functions can be substantially extended through alternative splicing.

Indexed as

Alternative SplicingRNA PrecursorsDatabases, GeneticGene Expression RegulationGenome, HumanHumansInternetModels, MolecularProtein ConformationProtein IsoformsProteinsProtein Sorting SignalsProtein Structure, TertiaryRNA SplicingProtein IsoformsProteinsProtein Sorting SignalsRNA Precursors

Identifiers

PMID17372197
PMCPMC1838448
OpenAlexW1971363517

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.