Evidence map›Paper›PMID 31723143›Full record

ArticleNature communications2019

The Firre locus produces a trans-acting RNA molecule that functions in hematopoiesis.

Jordan P Lewandowski, James C Lee, Taeyoung Hwang, Hongjae Sunwoo, Jill M Goldstein, Abigail F Groff, Nydia P Chang, William Mallard, Adam Williams, Jorge Henao-Meija and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

49 citing papers in PubMed, 80 citations in OpenAlex.

  1. Article
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  9. Profiling Molecular Changes of Host Response to Predict Outcome in Children with Septic Shock.Indian journal of critical care medicine : peer-reviewed, official publication of Indian Society of Critical Care Medicine · 2024
    Article
  10. Long non-coding RNAs involved inNAR genomics and bioinformatics · 2024
    Article
  11. Article
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  16. Multiomics analyses revealScience advances · 2023
    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

15 authors at 6 institutions in 2 countries.

Jordan P LewandowskiDepartment of Stem Cell and Regenerative Biology and Harvard Stem Cell Institute, Harvard University, Cambridge, MA, USA.
James C LeeDepartment of Stem Cell and Regenerative Biology and Harvard Stem Cell Institute, Harvard University, Cambridge, MA, USA.ORCID http://orcid.org/0000-0001-5711-9385
Taeyoung HwangDepartment of Stem Cell and Regenerative Biology and Harvard Stem Cell Institute, Harvard University, Cambridge, MA, USA.
Hongjae SunwooDepartment of Molecular Biology, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0001-8321-6269
Jill M GoldsteinDepartment of Stem Cell and Regenerative Biology and Harvard Stem Cell Institute, Harvard University, Cambridge, MA, USA.
Abigail F GroffDepartment of Stem Cell and Regenerative Biology and Harvard Stem Cell Institute, Harvard University, Cambridge, MA, USA.
Nydia P ChangDepartment of Stem Cell and Regenerative Biology and Harvard Stem Cell Institute, Harvard University, Cambridge, MA, USA.
William MallardDepartment of Stem Cell and Regenerative Biology and Harvard Stem Cell Institute, Harvard University, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-2271-945X
Adam WilliamsThe Jackson Laboratory, JAX Genomic Medicine, Farmington, CT, USA.
Jorge Henao-MeijaDepartment of Pathology and Laboratory Medicine, Perelman School of Medicine University of Pennsylvania, Philadelphia, PA, USA.
Richard A FlavellDepartment of Immunobiology and Howard Hughes Medical Institute, Yale University, School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0003-4461-0778
Jeannie T LeeDepartment of Molecular Biology, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0001-7786-8850
Chiara GerhardingerDepartment of Stem Cell and Regenerative Biology and Harvard Stem Cell Institute, Harvard University, Cambridge, MA, USA.
Amy J WagersDepartment of Stem Cell and Regenerative Biology and Harvard Stem Cell Institute, Harvard University, Cambridge, MA, USA.
John L RinnDepartment of Stem Cell and Regenerative Biology and Harvard Stem Cell Institute, Harvard University, Cambridge, MA, USA. john.rinn@colorado.edu.ORCID http://orcid.org/0000-0002-7231-7539
Harvard University · USHoward Hughes Medical Institute · USJackson Laboratory · USJoslin Diabetes Center · USMassachusetts General Hospital · USUniversity of Pennsylvania · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Regulatory Roles and Dynamics of Nuclear long-noncoding RNAs in PluripotencyP01GM099117 · NIGMS · HARVARD UNIVERSITY · PI MEISSNER, ALEXANDER · 2011 to 2021
$21.2M
Training Program in Angiogenesis &InflammationT32HL007893 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI DVORAK, HAROLD FISHER · 1998 to 2017
$5.5M
Regulation and Function of Growth Differentiation Factor 11 During Development and AgingR01AG048917 · NIA · HARVARD UNIVERSITY · PI WAGERS, AMY JO · 2016 to 2020
$2.8M
Functional Roles of Long Noncoding RNAs During Neuronal DevelopmentR01MH102416 · NIMH · HARVARD UNIVERSITY · PI ARLOTTA, PAOLA · 2014 to 2018
$2.1M
Regulation of Skeletal Muscle Regeneration During Aging by Growth Differentiation Factor 11F32AG050395 · NIA · HARVARD UNIVERSITY · PI GOLDSTEIN, JILL MARIE · 2015 to 2017
$121k
The Long Noncoding RNA Firre in Neural Development and DiseaseF32GM122335 · NIGMS · HARVARD UNIVERSITY · PI LEWANDOWSKI, JORDAN · 2017 to 2017
$57k
NCATS NIH HHS UL1 TR001863NHLBI NIH HHS T32 HL007893NIA NIH HHS F32 AG050395NIA NIH HHS R01 AG048917NIGMS NIH HHS F32 GM122335NIGMS NIH HHS P01 GM099117NIMH NIH HHS R01 MH102416Wellcome Trust
6 · The paper itself

Abstract

RNA has been classically known to play central roles in biology, including maintaining telomeres, protein synthesis, and in sex chromosome compensation. While thousands of long noncoding RNAs (lncRNAs) have been identified, attributing RNA-based roles to lncRNA loci requires assessing whether phenotype(s) could be due to DNA regulatory elements, transcription, or the lncRNA. Here, we use the conserved X chromosome lncRNA locus Firre, as a model to discriminate between DNA- and RNA-mediated effects in vivo. We demonstrate that (i) Firre mutant mice have cell-specific hematopoietic phenotypes, and (ii) upon exposure to lipopolysaccharide, mice overexpressing Firre exhibit increased levels of pro-inflammatory cytokines and impaired survival. (iii) Deletion of Firre does not result in changes in local gene expression, but rather in changes on autosomes that can be rescued by expression of transgenic Firre RNA. Together, our results provide genetic evidence that the Firre locus produces a trans-acting lncRNA that has physiological roles in hematopoiesis.

Indexed as

Genetic LociAnimalsFertilityGene Expression Regulation, DevelopmentalHematopoiesisImmunity, InnateLipopolysaccharidesMice, KnockoutOrgan SpecificityPhenotypeRNA, Long NoncodingFirre long non coding RNA, mouseLipopolysaccharidesRNA, Long Noncoding

Identifiers

PMID31723143
PMCPMC6853988
OpenAlexW2985271584

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.