Evidence map›Paper›PMID 26595768›Full record

ArticleNature genetics2016

The primate-specific noncoding RNA HPAT5 regulates pluripotency during human preimplantation development and nuclear reprogramming.

Jens Durruthy-Durruthy, Vittorio Sebastiano, Mark Wossidlo, Diana Cepeda, Jun Cui, Edward J Grow, Jonathan Davila, Moritz Mall, Wing H Wong, Joanna Wysocka and 2 more

Abstract read
In one paragraph

Article in Nature genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed
8.7field-weighted citation impact, top 1% 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

97 citing papers in PubMed, 190 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Functional Bidirectionality of ERV-Derived Long Non-Coding RNAs in Humans.International journal of molecular sciences · 2024
    Review
  8. SINE-Associated LncRNA SAWPA Regulates Porcine Zygotic Genome Activation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Long Non-coding RNAs and CRISPR-Cas Edition in Tumorigenesis.Advances in experimental medicine and biology · 2023
    Article
  14. Article
  15. Review
  16. Regulation of Embryonic Stem Cell Self-Renewal.Life (Basel, Switzerland) · 2022
    Review
  17. Article
  18. Review
  19. Designing libraries for pooled CRISPR functional screens of long noncoding RNAs.Mammalian genome : official journal of the International Mammalian Genome Society · 2022
    Review
  20. Review

37 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

12 authors at 2 institutions in 1 country.

Jens Durruthy-DurruthyInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, California, USA.
Vittorio SebastianoInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, California, USA.
Mark WossidloInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, California, USA.
Diana CepedaInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, California, USA.
Jun CuiInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, California, USA.ORCID http://orcid.org/0000-0002-1926-1759
Edward J GrowDepartment of Genetics, Stanford University, Stanford, California, USA.
Jonathan DavilaDepartment of Pathology, Stanford University, Stanford, California, USA.
Moritz MallDepartment of Pathology, Stanford University, Stanford, California, USA.
Wing H WongDepartment of Statistics, Stanford University, Stanford, California, USA.
Joanna WysockaDepartment of Chemical and Systems Biology, Stanford University, Stanford, California, USA.
Kin Fai AuDepartment of Statistics, Stanford University, Stanford, California, USA.
Renee A Reijo PeraInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, California, USA.
California Institute for Regenerative Medicine · USStanford University · US

Funding

INSTITUTIONAL TRAINING GRANT IN GENOME SCIENCET32HG000044 · NHGRI · STANFORD UNIVERSITY · PI MICHAEL P. SNYDER · 1995 to 2026
$32.2M
Basic and Translational Research iPSC-based hematologic and vascular therapiesU01HL100397 · NHLBI · STANFORD UNIVERSITY · PI COOKE, JOHN P · 2009 to 2015
$7.4M
Stanford University Center for Reproductive and Stem Cell biologyU54HD068158 · NICHD · STANFORD UNIVERSITY · PI HSUEH, AARON · 2011 to 2013
$5.0M
Stanford University Center for Reproductive and Stem Cell biologyP50HD068158 · NICHD · STANFORD UNIVERSITY · PI FULLER, MARGARET T · 2014 to 2015
$3.3M
Mechanisms of enhancer activation in early developmentR01GM112720 · NIGMS · STANFORD UNIVERSITY · PI WYSOCKA, JOANNA · 2015 to 2018
$1.2M
An approach to gene regulatory network inference.R01HG006018 · NHGRI · STANFORD UNIVERSITY · PI WONG, WING H. · 2011 to 2013
$1.1M
NHGRI NIH HHS R01 HG006018NHGRI NIH HHS R01HG006018NHGRI NIH HHS T32 HG000044NHLBI NIH HHS U01-1U01HL100397-01NHLBI NIH HHS U01 HL100397NICHD NIH HHS P50 HD068158NICHD NIH HHS U54-1U54HD068158-01NICHD NIH HHS U54 HD068158NIGMS NIH HHS R01 GM112720
6 · The paper itself

Abstract

Long intergenic noncoding RNAs (lincRNAs) are derived from thousands of loci in mammalian genomes and are frequently enriched in transposable elements (TEs). Although families of TE-derived lincRNAs have recently been implicated in the regulation of pluripotency, little is known of the specific functions of individual family members. Here we characterize three new individual TE-derived human lincRNAs, human pluripotency-associated transcripts 2, 3 and 5 (HPAT2, HPAT3 and HPAT5). Loss-of-function experiments indicate that HPAT2, HPAT3 and HPAT5 function in preimplantation embryo development to modulate the acquisition of pluripotency and the formation of the inner cell mass. CRISPR-mediated disruption of the genes for these lincRNAs in pluripotent stem cells, followed by whole-transcriptome analysis, identifies HPAT5 as a key component of the pluripotency network. Protein binding and reporter-based assays further demonstrate that HPAT5 interacts with the let-7 microRNA family. Our results indicate that unique individual members of large primate-specific lincRNA families modulate gene expression during development and differentiation to reinforce cell fate.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsBlastocystCell DifferentiationEmbryonic DevelopmentGene Knockdown TechniquesHumansMicroRNAsPluripotent Stem CellsPrimatesRNA, Long NoncodingSingle-Cell AnalysisMicroRNAsmirnlet7 microRNA, humanRNA, Long Noncoding

Identifiers

PMID26595768
PMCPMC4827613
OpenAlexW2177690692

What OpenQuestion holds

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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.