Evidence map›Paper›PMID 26546131›Full record

ArticleGenome research2016

Subcellular RNA profiling links splicing and nuclear DICER1 to alternative cleavage and polyadenylation.

Jonathan Neve, Kaspar Burger, Wencheng Li, Mainul Hoque, Radhika Patel, Bin Tian, Monika Gullerova, Andre Furger

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing 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

56 citing papers in PubMed, 83 citations in OpenAlex.

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  10. Downregulation of apoptotic repressorProceedings of the National Academy of Sciences of the United States of America · 2023
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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

8 authors at 2 institutions in 2 countries.

Jonathan NeveDepartment of Biochemistry, University of Oxford, OX1 3QU, United Kingdom;
Kaspar BurgerSir William Dunn School of Pathology, University of Oxford, OX1 3RE, United Kingdom;
Wencheng LiDepartment of Biochemistry and Molecular Biology, Rutgers New Jersey Medical School, Newark, New Jersey 07103, USA.
Mainul HoqueDepartment of Biochemistry and Molecular Biology, Rutgers New Jersey Medical School, Newark, New Jersey 07103, USA.
Radhika PatelDepartment of Biochemistry, University of Oxford, OX1 3QU, United Kingdom;
Bin TianDepartment of Biochemistry and Molecular Biology, Rutgers New Jersey Medical School, Newark, New Jersey 07103, USA.
Monika GullerovaSir William Dunn School of Pathology, University of Oxford, OX1 3RE, United Kingdom;
Andre FurgerDepartment of Biochemistry, University of Oxford, OX1 3QU, United Kingdom;
University of Oxford · GBRutgers, The State University of New Jersey · US

Funding

Regulation of Alternative Cleavage and PolyadenylationR01GM084089 · NIGMS · WISTAR INSTITUTE · PI TIAN, BIN · 2008 to 2023
$6.7M
Illumina NextSeq500 DNA Sequencing SystemS10OD018206 · OD · RBHS-NEW JERSEY MEDICAL SCHOOL · PI TIAN, BIN · 2015 to 2015
$227k
Medical Research Council 1243663Medical Research Council MR/K006606/1NIGMS NIH HHS GM 84089NIGMS NIH HHS R01 GM084089NIH HHS S10 OD018206
6 · The paper itself

Abstract

Alternative cleavage and polyadenylation (APA) plays a crucial role in the regulation of gene expression across eukaryotes. Although APA is extensively studied, its regulation within cellular compartments and its physiological impact remains largely enigmatic. Here, we used a rigorous subcellular fractionation approach to compare APA profiles of cytoplasmic and nuclear RNA fractions from human cell lines. This approach allowed us to extract APA isoforms that are subjected to differential regulation and provided us with a platform to interrogate the molecular regulatory pathways that shape APA profiles in different subcellular locations. Here, we show that APA isoforms with shorter 3' UTRs tend to be overrepresented in the cytoplasm and appear to be cell-type-specific events. Nuclear retention of longer APA isoforms occurs and is partly a result of incomplete splicing contributing to the observed cytoplasmic bias of transcripts with shorter 3' UTRs. We demonstrate that the endoribonuclease III, DICER1, contributes to the establishment of subcellular APA profiles not only by expected cytoplasmic miRNA-mediated destabilization of APA mRNA isoforms, but also by affecting polyadenylation site choice.

Indexed as

Gene Expression ProfilingPolyadenylationRNA Splicing3' Untranslated RegionsDEAD-box RNA HelicasesGene Expression RegulationGenome, HumanHEK293 CellsHigh-Throughput Nucleotide SequencingHumansMetallochaperonesMicroRNAsProtein IsoformsRibonuclease IIIRNA Stability3' Untranslated RegionsCIAO1 protein, humanDEAD-box RNA HelicasesDICER1 protein, humanMetallochaperonesMicroRNAsProtein IsoformsRibonuclease III

Identifiers

PMID26546131
PMCPMC4691748
OpenAlexW2171385508

What OpenQuestion holds

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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.