Evidence map›Paper›PMID 25313066›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Argonaute-1 binds transcriptional enhancers and controls constitutive and alternative splicing in human cells.

Mariano Alló, Eneritz Agirre, Sergey Bessonov, Paola Bertucci, Luciana Gómez Acuña, Valeria Buggiano, Nicolás Bellora, Babita Singh, Ezequiel Petrillo, Matías Blaustein and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

62 citing papers in PubMed, 105 citations in OpenAlex.

  1. Article
  2. Review
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  7. Article
  8. Noncanonical functions of microRNAs in the nucleus.Acta biochimica et biophysica Sinica · 2024
    Review
  9. Review
  10. Age and 17β-Estradiol (ENon-coding RNA · 2023
    Article
  11. Review
  12. Review
  13. Article
  14. Article
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  17. Article
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  19. Article
  20. Noncoding RNAs in apoptosis: identification and function.Turkish journal of biology = Turk biyoloji dergisi · 2022
    Review

2 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

21 authors at 4 institutions in 3 countries.

Mariano AllóLaboratorio de Fisiología y Biología Molecular, Departamento de Fisiología, Biología Molecular y Celular, Instituto de Fisiología, Biología Molecular y Neurociencias-Consejo Nacional de Investigaciones Científicas y Técnicas, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, C1428EHA Buenos Aires, Argentina;
Eneritz AgirreComputational Genomics, Universitat Pompeu Fabra, E-08003 Barcelona, Spain;
Sergey BessonovMax Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany;
Paola BertucciLaboratorio de Fisiología y Biología Molecular, Departamento de Fisiología, Biología Molecular y Celular, Instituto de Fisiología, Biología Molecular y Neurociencias-Consejo Nacional de Investigaciones Científicas y Técnicas, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, C1428EHA Buenos Aires, Argentina;
Luciana Gómez AcuñaLaboratorio de Fisiología y Biología Molecular, Departamento de Fisiología, Biología Molecular y Celular, Instituto de Fisiología, Biología Molecular y Neurociencias-Consejo Nacional de Investigaciones Científicas y Técnicas, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, C1428EHA Buenos Aires, Argentina;
Valeria BuggianoLaboratorio de Fisiología y Biología Molecular, Departamento de Fisiología, Biología Molecular y Celular, Instituto de Fisiología, Biología Molecular y Neurociencias-Consejo Nacional de Investigaciones Científicas y Técnicas, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, C1428EHA Buenos Aires, Argentina;
Nicolás BelloraComputational Genomics, Universitat Pompeu Fabra, E-08003 Barcelona, Spain;
Babita SinghComputational Genomics, Universitat Pompeu Fabra, E-08003 Barcelona, Spain;
Ezequiel PetrilloLaboratorio de Fisiología y Biología Molecular, Departamento de Fisiología, Biología Molecular y Celular, Instituto de Fisiología, Biología Molecular y Neurociencias-Consejo Nacional de Investigaciones Científicas y Técnicas, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, C1428EHA Buenos Aires, Argentina;
Matías BlausteinLaboratorio de Fisiología y Biología Molecular, Departamento de Fisiología, Biología Molecular y Celular, Instituto de Fisiología, Biología Molecular y Neurociencias-Consejo Nacional de Investigaciones Científicas y Técnicas, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, C1428EHA Buenos Aires, Argentina;
Belén MiñanaComputational Genomics, Universitat Pompeu Fabra, E-08003 Barcelona, Spain; Centre for Genomic Regulation, E-08003 Barcelona, Spain; and.
Gwendal DujardinLaboratorio de Fisiología y Biología Molecular, Departamento de Fisiología, Biología Molecular y Celular, Instituto de Fisiología, Biología Molecular y Neurociencias-Consejo Nacional de Investigaciones Científicas y Técnicas, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, C1428EHA Buenos Aires, Argentina;
Berta PozziLaboratorio de Fisiología y Biología Molecular, Departamento de Fisiología, Biología Molecular y Celular, Instituto de Fisiología, Biología Molecular y Neurociencias-Consejo Nacional de Investigaciones Científicas y Técnicas, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, C1428EHA Buenos Aires, Argentina;
Federico PelischLaboratorio de Fisiología y Biología Molecular, Departamento de Fisiología, Biología Molecular y Celular, Instituto de Fisiología, Biología Molecular y Neurociencias-Consejo Nacional de Investigaciones Científicas y Técnicas, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, C1428EHA Buenos Aires, Argentina;
Elías BecharaComputational Genomics, Universitat Pompeu Fabra, E-08003 Barcelona, Spain; Centre for Genomic Regulation, E-08003 Barcelona, Spain; and.
Dmitry E AgafonovMax Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany;
Anabella SrebrowLaboratorio de Fisiología y Biología Molecular, Departamento de Fisiología, Biología Molecular y Celular, Instituto de Fisiología, Biología Molecular y Neurociencias-Consejo Nacional de Investigaciones Científicas y Técnicas, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, C1428EHA Buenos Aires, Argentina;
Reinhard LührmannMax Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany;
Juan ValcárcelComputational Genomics, Universitat Pompeu Fabra, E-08003 Barcelona, Spain; Centre for Genomic Regulation, E-08003 Barcelona, Spain; and Catalan Institution for Research and Advanced Studies, E-08010 Barcelona, Spain.
Eduardo EyrasComputational Genomics, Universitat Pompeu Fabra, E-08003 Barcelona, Spain; Catalan Institution for Research and Advanced Studies, E-08010 Barcelona, Spain eduardo.eyras@upf.edu ark@fbmc.fcen.uba.ar.
Alberto R KornblihttLaboratorio de Fisiología y Biología Molecular, Departamento de Fisiología, Biología Molecular y Celular, Instituto de Fisiología, Biología Molecular y Neurociencias-Consejo Nacional de Investigaciones Científicas y Técnicas, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, C1428EHA Buenos Aires, Argentina; eduardo.eyras@upf.edu ark@fbmc.fcen.uba.ar.
University of Buenos Aires · ARPompeu Fabra University · ESFundación Ciencias Exactas y Naturales · ARMax Planck Institute for Biophysical Chemistry · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The roles of Argonaute proteins in cytoplasmic microRNA and RNAi pathways are well established. However, their implication in small RNA-mediated transcriptional gene silencing in the mammalian cell nucleus is less understood. We have recently shown that intronic siRNAs cause chromatin modifications that inhibit RNA polymerase II elongation and modulate alternative splicing in an Argonaute-1 (AGO1)-dependent manner. Here we used chromatin immunoprecipitation followed by deep sequencing (ChIP-seq) to investigate the genome-wide distribution of AGO1 nuclear targets. Unexpectedly, we found that about 80% of AGO1 clusters are associated with cell-type-specific transcriptional enhancers, most of them (73%) overlapping active enhancers. This association seems to be mediated by long, rather than short, enhancer RNAs and to be more prominent in intragenic, rather than intergenic, enhancers. Paradoxically, crossing ChIP-seq with RNA-seq data upon AGO1 depletion revealed that enhancer-bound AGO1 is not linked to the global regulation of gene transcription but to the control of constitutive and alternative splicing, which was confirmed by an individual gene analysis explaining how AGO1 controls inclusion levels of the cassette exon 107 in the SYNE2 gene.

Indexed as

Alternative SplicingArgonaute ProteinsCell LineEnhancer Elements, GeneticEukaryotic Initiation FactorsGene Expression RegulationHumansRNASequence Analysis, RNATranscription, GeneticAGO1 protein, humanArgonaute ProteinsEukaryotic Initiation FactorsRNAalternative splicingArgonaute proteinstranscriptional enhancers

Identifiers

PMID25313066
PMCPMC4226100
OpenAlexW2058004141

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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.