Evidence map›Paper›PMID 28102192›Full record

ArticleNature communications2017

The impact of microRNAs on transcriptional heterogeneity and gene co-expression across single embryonic stem cells.

Gennaro Gambardella, Annamaria Carissimo, Amy Chen, Luisa Cutillo, Tomasz J Nowakowski, Diego di Bernardo, Robert Blelloch

Abstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
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  9. The multifaceted roles of microRNAs in differentiation.Current opinion in cell biology · 2020
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Regulation of stomatal development by stomatal lineage miRNAs.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  15. Review
  16. Up-regulation of miR-155 contributes to TNF-mediated hepatocyte apoptosis in acute liver failure.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2019
    Article
  17. Review
  18. Article
  19. 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

7 authors.

Gennaro GambardellaTelethon Institute of Genetics and Medicine, Pozzuoli, 80078 Naples, Italy.
Annamaria CarissimoTelethon Institute of Genetics and Medicine, Pozzuoli, 80078 Naples, Italy.
Amy ChenThe Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, Center for Reproductive Sciences, University of California, San Francisco, San Francisco, California 94143, USA.
Luisa CutilloTelethon Institute of Genetics and Medicine, Pozzuoli, 80078 Naples, Italy.
Tomasz J NowakowskiThe Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, Center for Reproductive Sciences, University of California, San Francisco, San Francisco, California 94143, USA.
Diego di BernardoTelethon Institute of Genetics and Medicine, Pozzuoli, 80078 Naples, Italy.ORCID 0000-0002-1911-7407
Robert BlellochThe Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, Center for Reproductive Sciences, University of California, San Francisco, San Francisco, California 94143, USA.

Funding

Research BaseP30DK063720 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRUMMEL, MATTHEW F · 2003 to 2019
$21.8M
PREDOCTORAL TRAINING IN BIOMEDICAL SCIENCEST32GM008568 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ANSEL, KARL MARK · 1995 to 2019
$6.3M
NIDDK NIH HHS P30 DK063720NIGMS NIH HHS T32 GM008568Telethon TGM11SB1
6 · The paper itself

Abstract

MicroRNAs act posttranscriptionally to suppress multiple target genes within a cell population. To what extent this multi-target suppression occurs in individual cells and how it impacts transcriptional heterogeneity and gene co-expression remains unknown. Here we used single-cell sequencing combined with introduction of individual microRNAs. miR-294 and let-7c were introduced into otherwise microRNA-deficient Dgcr8 knockout mouse embryonic stem cells. Both microRNAs induce suppression and correlated expression of their respective gene targets. The two microRNAs had opposing effects on transcriptional heterogeneity within the cell population, with let-7c increasing and miR-294 decreasing the heterogeneity between cells. Furthermore, let-7c promotes, whereas miR-294 suppresses, the phasing of cell cycle genes. These results show at the individual cell level how a microRNA simultaneously has impacts on its many targets and how that in turn can influence a population of cells. The findings have important implications in the understanding of how microRNAs influence the co-expression of genes and pathways, and thus ultimately cell fate.

Indexed as

AnimalsCell CycleCell SizeEmbryonic Stem CellsGene Expression RegulationMiceMice, KnockoutMicroRNAsPrincipal Component AnalysisRNA-Binding ProteinsSingle-Cell AnalysisTranscription, GeneticDgcr8 protein, mouseMicroRNAsRNA-Binding Proteins

Identifiers

PMID28102192
PMCPMC5253645

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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.