Evidence map›Paper›PMID 31796550›Full record

ReviewGenetics2019

Multimodal Long Noncoding RNA Interaction Networks: Control Panels for Cell Fate Specification.

Keriayn N Smith, Sarah C Miller, Gabriele Varani, J Mauro Calabrese, Terry Magnuson

Abstract readReview
In one paragraph

Review in Genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
  2. Article
  3. A long noncoding RNA at theProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Review
  5. Article
  6. Review
  7. Host gene and its guest: short story about relation of long-noncodingReports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology · 2023
    Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. International journal of biological sciences · 2020
    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

5 authors.

Keriayn N Smith *Department of Genetics, University of North Carolina, Chapel Hill, North Carolina 27599 kns@email.unc.edu.ORCID 0000-0002-4351-2765
Sarah C Miller *Department of Genetics, University of North Carolina, Chapel Hill, North Carolina 27599.ORCID 0000-0003-3470-8798
Gabriele VaraniDepartment of Chemistry, University of Washington, Seattle, Washington 98195.ORCID 0000-0001-6642-7144
J Mauro CalabreseDepartment of Pharmacology, University of North Carolina, Chapel Hill, North Carolina 27599.ORCID 0000-0002-1213-2540
Terry MagnusonDepartment of Genetics, University of North Carolina, Chapel Hill, North Carolina 27599.ORCID 0000-0002-0792-835X

Funding

ncRNA: Structure, Interactions and InhibitionR35GM126942 · NIGMS · UNIVERSITY OF WASHINGTON · PI Gabriele Varani · 2018 to 2026
$6.0M
Albino Deletion Complex and Early Mouse DevelopmentR01GM101974 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MAGNUSON, TERRY R · 2012 to 2024
$5.2M
Mechanisms of gene silencing induced by long noncoding RNAsR01GM121806 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CALABRESE, JOSEPH MAURO · 2017 to 2023
$2.3M
Regulation of microRNA processingR01GM103834 · NIGMS · UNIVERSITY OF WASHINGTON · PI VARANI, GABRIELE · 2014 to 2017
$1.1M
Integrative Analysis of a Long Noncoding RNA Functional Network in PluripotencyR03HD093977 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SMITH, KERIAYN · 2018 to 2019
$156k
NICHD NIH HHS R03 HD093977NIGMS NIH HHS R01 GM101974NIGMS NIH HHS R01 GM103834NIGMS NIH HHS R01 GM121806NIGMS NIH HHS R35 GM126942
6 · The paper itself

Abstract

Lineage specification in early development is the basis for the exquisitely precise body plan of multicellular organisms. It is therefore critical to understand cell fate decisions in early development. Moreover, for regenerative medicine, the accurate specification of cell types to replace damaged/diseased tissue is strongly dependent on identifying determinants of cell identity. Long noncoding RNAs (lncRNAs) have been shown to regulate cellular plasticity, including pluripotency establishment and maintenance, differentiation and development, yet broad phenotypic analysis and the mechanistic basis of their function remains lacking. As components of molecular condensates, lncRNAs interact with almost all classes of cellular biomolecules, including proteins, DNA, mRNAs, and microRNAs. With functions ranging from controlling alternative splicing of mRNAs, to providing scaffolding upon which chromatin modifiers are assembled, it is clear that at least a subset of lncRNAs are far from the transcriptional noise they were once deemed. This review highlights the diversity of lncRNA interactions in the context of cell fate specification, and provides examples of each type of interaction in relevant developmental contexts. Also highlighted are experimental and computational approaches to study lncRNAs.

Indexed as

Gene Regulatory NetworksCell LineageChromatinHumansModels, BiologicalProtein StabilityRNA, Long NoncodingChromatinRNA, Long Noncodingcell fate specificationcompeting endogenous RNAsk-merslong noncoding RNAsmiRNAs

Identifiers

PMID31796550
PMCPMC6893379

What OpenQuestion holds

Textmetadata
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.