Evidence map›Paper›PMID 33274830›Full record

ArticleAging cell2020

Prevalent intron retention fine-tunes gene expression and contributes to cellular senescence.

Jun Yao, Dong Ding, Xueping Li, Ting Shen, Haihui Fu, Hua Zhong, Gang Wei, Ting Ni

Abstract read
In one paragraph

Article in Aging cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

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  15. Hypertrophic cardiomyopathy inThe journal of cardiovascular aging · 2024
    Article
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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.

Jun YaoState Key Laboratory of Genetic Engineering, Collaborative Innovation Center of Genetics and Development, Human Phenome Institute, School of Life Sciences, Fudan University, Shanghai, P.R. China.ORCID 0000-0002-5970-8375
Dong DingState Key Laboratory of Genetic Engineering, Collaborative Innovation Center of Genetics and Development, Human Phenome Institute, School of Life Sciences, Fudan University, Shanghai, P.R. China.
Xueping LiState Key Laboratory of Genetic Engineering, Collaborative Innovation Center of Genetics and Development, Human Phenome Institute, School of Life Sciences, Fudan University, Shanghai, P.R. China.
Ting ShenState Key Laboratory of Genetic Engineering, Collaborative Innovation Center of Genetics and Development, Human Phenome Institute, School of Life Sciences, Fudan University, Shanghai, P.R. China.
Haihui FuState Key Laboratory of Genetic Engineering, Collaborative Innovation Center of Genetics and Development, Human Phenome Institute, School of Life Sciences, Fudan University, Shanghai, P.R. China.
Hua ZhongDepartment of Population Health, NYU Langone School of Medicine, New York, NY, USA.
Gang WeiState Key Laboratory of Genetic Engineering, Collaborative Innovation Center of Genetics and Development, Human Phenome Institute, School of Life Sciences, Fudan University, Shanghai, P.R. China.
Ting NiState Key Laboratory of Genetic Engineering, Collaborative Innovation Center of Genetics and Development, Human Phenome Institute, School of Life Sciences, Fudan University, Shanghai, P.R. China.ORCID 0000-0001-7007-1072

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intron retention (IR) is the least well-understood alternative splicing type in animals, and its prevalence and function in physiological and pathological processes have long been underestimated. Cellular senescence contributes to individual aging and age-related diseases and can also serve as an important cancer prevention mechanism. Dynamic IR events have been observed in senescence models and aged tissues; however, whether and how IR impacts senescence remain unclear. Through analyzing polyA

Indexed as

IntronsAlternative SplicingBinding SitesCalcium-Binding ProteinsCells, CulturedCellular SenescenceDown-RegulationGene ExpressionGene Knockdown TechniquesHumansModels, BiologicalRNA-Binding ProteinsRNA-SeqSplicing Factor U2AFCalcium-Binding ProteinsCPNE1 protein, humanRNA-Binding ProteinsSplicing Factor U2AFU2AF1 protein, humanCPNE1intron retentionsenescencesplicing factorU2AF1

Identifiers

PMID33274830
PMCPMC7744961

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.