Evidence map›Paper›PMID 28820723›Full record

ArticleeLife2017

A lncRNA fine tunes the dynamics of a cell state transition involving

Meng Amy Li, Paulo P Amaral, Priscilla Cheung, Jan H Bergmann, Masaki Kinoshita, Tüzer Kalkan, Meryem Ralser, Sam Robson, Ferdinand von Meyenn, Maike Paramor and 7 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

33 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
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  12. RNA-Chrom: a manually curated analytical database of RNA-chromatin interactome.Database : the journal of biological databases and curation · 2023
    Article
  13. Review
  14. LncRNA-mediated DNA methylation: an emerging mechanism in cancer and beyond.Journal of experimental & clinical cancer research : CR · 2022
    Review
  15. Review
  16. Article
  17. Article
  18. Disabling de novo DNA methylation in embryonic stem cells allows an illegitimate fate trajectory.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  19. Article
  20. Article
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

17 authors at 7 institutions in 2 countries.

Meng Amy LiWellcome Trust - Medical Research Council Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0002-6619-9919
Paulo P AmaralThe Gurdon Institute, University of Cambridge, Cambridge, United Kingdom.
Priscilla CheungDivision of Cellular and Developmental Biology, Department of Molecular and Cellular Biology, University of California Berkeley, Berkeley, United States.
Jan H BergmannCold Spring Harbor Laboratory, Cold Spring Harbor, United States.
Masaki KinoshitaWellcome Trust - Medical Research Council Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom.
Tüzer KalkanWellcome Trust - Medical Research Council Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom.
Meryem RalserWellcome Trust - Medical Research Council Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom.
Sam RobsonThe Gurdon Institute, University of Cambridge, Cambridge, United Kingdom.
Ferdinand von MeyennBabraham Institute, Cambridge, United Kingdom.
Maike ParamorWellcome Trust - Medical Research Council Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom.
Fengtang YangWellcome Trust Sanger Institute, Hinxton, United Kingdom.
Caifu ChenIntegrated DNA Technologies, Redwood, United States.
Jennifer NicholsWellcome Trust - Medical Research Council Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom.
David L SpectorCold Spring Harbor Laboratory, Cold Spring Harbor, United States.
Tony KouzaridesThe Gurdon Institute, University of Cambridge, Cambridge, United Kingdom.
Lin HeDivision of Cellular and Developmental Biology, Department of Molecular and Cellular Biology, University of California Berkeley, Berkeley, United States.
Austin SmithWellcome Trust - Medical Research Council Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0002-3029-4682
Wellcome/MRC Cambridge Stem Cell Institute · GBUniversity of Cambridge · GBCold Spring Harbor Laboratory · USUniversity of California, Berkeley · USBabraham Institute · GBIntegrated DNA Technologies (United States) · USWellcome Sanger Institute · GB

Funding

Single-Cell Biology Shared ResourceP30CA045508 · NCI · COLD SPRING HARBOR LABORATORY · PI John Edward Moses · 1987 to 2026
$118.9M
VIRAL TRANSACTIVATIONP01CA013106 · NCI · COLD SPRING HARBOR LABORATORY · PI William Richard McCombie · 1985 to 2026
$116.8M
miR-200 miRNAs repress tumor metastasis in lung adenocarcinomaR01CA139067 · NCI · UNIVERSITY OF CALIFORNIA BERKELEY · PI HE, LIN · 2009 to 2021
$3.3M
A new technology to isolate RNP complexes of a polycistronic miRNA oncogeneR21CA175560 · NCI · UNIVERSITY OF CALIFORNIA BERKELEY · PI HE, LIN · 2013 to 2014
$360k
Biotechnology and Biological Sciences Research Council BB/M004023/1Cancer Research UK 10827Cancer Research UK 17001Cancer Research UK C6946/A14492Cancer Research UK C6/A18796Medical Research Council G1100526Medical Research Council MC_PC_12009NCI NIH HHS P01 CA013106NCI NIH HHS P30 CA045508NCI NIH HHS R01 CA139067NCI NIH HHS R21 CA175560Wellcome TrustWellcome Trust 091484/Z/10/ZWellcome Trust 092096Wellcome Trust 096125/Z/11/Z
6 · The paper itself

Abstract

Execution of pluripotency requires progression from the naïve status represented by mouse embryonic stem cells (ESCs) to a state capacitated for lineage specification. This transition is coordinated at multiple levels. Non-coding RNAs may contribute to this regulatory orchestra. We identified a rodent-specific long non-coding RNA (lncRNA)

Indexed as

Cell DifferentiationDNA MethylationGene Expression RegulationAnimalsDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3ADNA Methyltransferase 3BGene DeletionMiceMicroRNAsMouse Embryonic Stem CellsRNA-Binding ProteinsRNA, Long NoncodingDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3ADNA Methyltransferase 3BDnmt3a protein, mouseLin-28 protein, mouseMicroRNAsmirnlet7 microRNA, mouseRNA-Binding ProteinsRNA, Long Noncodingde novo DNA methylationdevelopmental biologyLin28a/Mirlet7long non-coding RNAmousepluripotencystem cellsstem cell transition

Identifiers

PMID28820723
PMCPMC5562443
OpenAlexW2743376548

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.