Evidence map›Paper›PMID 25934563›Full record

ArticleGenome research2015

Unmasking alternative splicing inside protein-coding exons defines exitrons and their role in proteome plasticity.

Yamile Marquez, Markus Höpfler, Zahra Ayatollahi, Andrea Barta, Maria Kalyna

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing 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

99 citing papers in PubMed, 168 citations in OpenAlex.

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  14. Exitron splicing of odor receptor genes inProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  15. Review
  16. Review
  17. Responsive Alternative Splicing Events ofInternational journal of molecular sciences · 2024
    Article
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  20. Review

39 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Yamile MarquezMax F. Perutz Laboratories, Medical University of Vienna, Vienna A-1030, Austria;
Markus HöpflerMax F. Perutz Laboratories, Medical University of Vienna, Vienna A-1030, Austria;
Zahra AyatollahiMax F. Perutz Laboratories, Medical University of Vienna, Vienna A-1030, Austria;
Andrea BartaMax F. Perutz Laboratories, Medical University of Vienna, Vienna A-1030, Austria;
Maria KalynaMax F. Perutz Laboratories, Medical University of Vienna, Vienna A-1030, Austria; Department of Applied Genetics and Cell Biology, BOKU - University of Natural Resources and Life Sciences, Vienna A-1190, Austria.
Medical University of Vienna · ATMax Perutz Labs · AT

Funding

Austrian Science Fund FWF P 26333
6 · The paper itself

Abstract

Alternative splicing (AS) diversifies transcriptomes and proteomes and is widely recognized as a key mechanism for regulating gene expression. Previously, in an analysis of intron retention events in Arabidopsis, we found unusual AS events inside annotated protein-coding exons. Here, we also identify such AS events in human and use these two sets to analyse their features, regulation, functional impact, and evolutionary origin. As these events involve introns with features of both introns and protein-coding exons, we name them exitrons (exonic introns). Though exitrons were detected as a subset of retained introns, they are clearly distinguishable, and their splicing results in transcripts with different fates. About half of the 1002 Arabidopsis and 923 human exitrons have sizes of multiples of 3 nucleotides (nt). Splicing of these exitrons results in internally deleted proteins and affects protein domains, disordered regions, and various post-translational modification sites, thus broadly impacting protein function. Exitron splicing is regulated across tissues, in response to stress and in carcinogenesis. Intriguingly, annotated intronless genes can be also alternatively spliced via exitron usage. We demonstrate that at least some exitrons originate from ancestral coding exons. Based on our findings, we propose a "splicing memory" hypothesis whereby upon intron loss imprints of former exon borders defined by vestigial splicing regulatory elements could drive the evolution of exitron splicing. Altogether, our studies show that exitron splicing is a conserved strategy for increasing proteome plasticity in plants and animals, complementing the repertoire of AS events.

Indexed as

Alternative SplicingExonsIntronsOpen Reading FramesProteomicsArabidopsisBreast NeoplasmsEvolution, MolecularFemaleGene Expression Regulation, PlantHumansOrgan SpecificityProtein BiosynthesisRNA TransportStress, PhysiologicalTranscriptome

Identifiers

PMID25934563
PMCPMC4484396
OpenAlexW2101772746

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.