Evidence map›Paper›PMID 35293570›Full record

ArticleNucleic acids research2022

Dysregulated RNA polyadenylation contributes to metabolic impairment in non-alcoholic fatty liver disease.

Andrew M Jobbins, Nejc Haberman, Natalia Artigas, Christopher Amourda, Helen A B Paterson, Sijia Yu, Samuel J I Blackford, Alex Montoya, Marian Dore, Yi-Fang Wang and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  6. Review
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  8. Review
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  11. Research Progress of Alternative Polyadenylation in Diseases Related to Glycolipid Metabolism.Diabetes, metabolic syndrome and obesity : targets and therapy · 2024
    Review
  12. Article
  13. Article
  14. Review
  15. Article
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  17. Review
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

16 authors at 3 institutions in 2 countries.

Andrew M JobbinsMRC London Institute of Medical Sciences, Du Cane Road, London W12 0NN, UK.
Nejc HabermanMRC London Institute of Medical Sciences, Du Cane Road, London W12 0NN, UK.
Natalia ArtigasMRC London Institute of Medical Sciences, Du Cane Road, London W12 0NN, UK.
Christopher AmourdaMRC London Institute of Medical Sciences, Du Cane Road, London W12 0NN, UK.
Helen A B PatersonMRC London Institute of Medical Sciences, Du Cane Road, London W12 0NN, UK.
Sijia YuMRC London Institute of Medical Sciences, Du Cane Road, London W12 0NN, UK.
Samuel J I BlackfordDepartment of Metabolism, Digestion & Reproduction, Imperial College London, London W12 0NN, UK.
Alex MontoyaMRC London Institute of Medical Sciences, Du Cane Road, London W12 0NN, UK.
Marian DoreMRC London Institute of Medical Sciences, Du Cane Road, London W12 0NN, UK.
Yi-Fang WangMRC London Institute of Medical Sciences, Du Cane Road, London W12 0NN, UK.
Alessandro SardiniMRC London Institute of Medical Sciences, Du Cane Road, London W12 0NN, UK.
Inês CebolaSection of Genetics and Genomics, Department of Metabolism, Digestion & Reproduction, Imperial College London, London W12 0NN, UK.
Johannes ZuberResearch Institute of Molecular Pathology (IMP), Vienna BioCenter (VBC), 1030 Vienna, Austria.
Sheikh Tamir RashidDepartment of Metabolism, Digestion & Reproduction, Imperial College London, London W12 0NN, UK.
Boris LenhardMRC London Institute of Medical Sciences, Du Cane Road, London W12 0NN, UK.ORCID 0000-0002-1114-1509
Santiago VerniaMRC London Institute of Medical Sciences, Du Cane Road, London W12 0NN, UK.ORCID 0000-0001-6728-5555
Hammersmith Hospital · GBImperial College London · GBResearch Institute of Molecular Pathology · AT

Funding

British Heart FoundationDepartment of HealthMedical Research Council MC_UP_1102/1Medical Research Council MC_UP_1102/18Wellcome Trust
6 · The paper itself

Abstract

Pre-mRNA processing is an essential mechanism for the generation of mature mRNA and the regulation of gene expression in eukaryotic cells. While defects in pre-mRNA processing have been implicated in a number of diseases their involvement in metabolic pathologies is still unclear. Here, we show that both alternative splicing and alternative polyadenylation, two major steps in pre-mRNA processing, are significantly altered in non-alcoholic fatty liver disease (NAFLD). Moreover, we find that Serine and Arginine Rich Splicing Factor 10 (SRSF10) binding is enriched adjacent to consensus polyadenylation motifs and its expression is significantly decreased in NAFLD, suggesting a role mediating pre-mRNA dysregulation in this condition. Consistently, inactivation of SRSF10 in mouse and human hepatocytes in vitro, and in mouse liver in vivo, was found to dysregulate polyadenylation of key metabolic genes such as peroxisome proliferator-activated receptor alpha (PPARA) and exacerbate diet-induced metabolic dysfunction. Collectively our work implicates dysregulated pre-mRNA polyadenylation in obesity-induced liver disease and uncovers a novel role for SRSF10 in this process.

Indexed as

Non-alcoholic Fatty Liver DiseasePolyadenylationAnimalsCell Cycle ProteinsHepatocytesHumansLiverMiceRepressor ProteinsRNA PrecursorsRNA SplicingSerine-Arginine Splicing FactorsCell Cycle ProteinsRepressor ProteinsRNA PrecursorsSerine-Arginine Splicing FactorsSRSF10 protein, mouse

Identifiers

PMID35293570
PMCPMC8989518
OpenAlexW4220996167

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.