Evidence map›Paper›PMID 31724706›Full record

ReviewNucleic acids research2019

The changing paradigm of intron retention: regulation, ramifications and recipes.

Geoffray Monteuuis, Justin J L Wong, Charles G Bailey, Ulf Schmitz, John E J Rasko

Abstract readReview
In one paragraph

Review in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 131 papers.

0numbers the graph read from it
0cells of the map it votes in
131citing 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

131 citing papers in PubMed.

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  19. Intron Retention Controls Localization of lncRNAsbioRxiv : the preprint server for biology · 2026
    Article
  20. Article

71 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

5 authors.

Geoffray MonteuuisGene and Stem Cell Therapy Program Centenary Institute, The University of Sydney, Camperdown, Australia.
Justin J L WongFaculty of Medicine and Health, The University of Sydney, NSW 2006, Australia.
Charles G BaileyGene and Stem Cell Therapy Program Centenary Institute, The University of Sydney, Camperdown, Australia.
Ulf SchmitzGene and Stem Cell Therapy Program Centenary Institute, The University of Sydney, Camperdown, Australia.
John E J RaskoGene and Stem Cell Therapy Program Centenary Institute, The University of Sydney, Camperdown, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intron retention (IR) is a form of alternative splicing that has long been neglected in mammalian systems although it has been studied for decades in non-mammalian species such as plants, fungi, insects and viruses. It was generally assumed that mis-splicing, leading to the retention of introns, would have no physiological consequence other than reducing gene expression by nonsense-mediated decay. Relatively recent landmark discoveries have highlighted the pivotal role that IR serves in normal and disease-related human biology. Significant technical hurdles have been overcome, thereby enabling the robust detection and quantification of IR. Still, relatively little is known about the cis- and trans-acting modulators controlling this phenomenon. The fate of an intron to be, or not to be, retained in the mature transcript is the direct result of the influence exerted by numerous intrinsic and extrinsic factors at multiple levels of regulation. These factors have altered current biological paradigms and provided unexpected insights into the transcriptional landscape. In this review, we discuss the regulators of IR and methods to identify them. Our focus is primarily on mammals, however, we broaden the scope to non-mammalian organisms in which IR has been shown to be biologically relevant.

Indexed as

Alternative SplicingAnimalsBacteriaEpigenesis, GeneticFungiGene Expression RegulationHumansIntronsNonsense Mediated mRNA DecayRegulatory Sequences, Ribonucleic AcidRNA, MessengerRegulatory Sequences, Ribonucleic AcidRNA, Messenger

Identifiers

PMID31724706
PMCPMC7145568

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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.