Evidence map›Paper›PMID 25887447›Full record

ArticleGenome biology2015

The lncRNA Firre anchors the inactive X chromosome to the nucleolus by binding CTCF and maintains H3K27me3 methylation.

Fan Yang, Xinxian Deng, Wenxiu Ma, Joel B Berletch, Natalia Rabaia, Gengze Wei, James M Moore, Galina N Filippova, Jun Xu, Yajuan Liu and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Genome biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 168 papers.

0numbers the graph read from it
0cells of the map it votes in
168citing papers in PubMed
11.4field-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

168 citing papers in PubMed, 270 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Genome research · 2025
    Article
  9. Article
  10. A haplotype-resolved view of human gene regulation.bioRxiv : the preprint server for biology · 2025
    Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

108 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

13 authors at 3 institutions in 1 country.

Fan YangDepartment of Pathology, University of Washington, Seattle, Washington, 98195, USA. fyang8191@gmail.com.
Xinxian DengDepartment of Pathology, University of Washington, Seattle, Washington, 98195, USA. dengx2@uw.edu.
Wenxiu MaDepartment of Genome Sciences, University of Washington, Seattle, Washington, 98195, USA. wenxiu@uw.edu.
Joel B BerletchDepartment of Pathology, University of Washington, Seattle, Washington, 98195, USA. joelb07@u.washington.edu.
Natalia RabaiaDivision of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington, 98109, USA. nrabaia@fhcrc.org.
Gengze WeiDepartment of Integrative Physiology and Neuroscience, Washington State University, Pullman, Washington, 99164, USA. weigengze@vetmed.wsu.edu.
James M MooreDivision of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington, 98109, USA. jmmoore@fhcrc.org.
Galina N FilippovaDivision of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington, 98109, USA. gfilippo@fhcrc.org.
Jun XuDepartment of Integrative Physiology and Neuroscience, Washington State University, Pullman, Washington, 99164, USA. junxu@vetmed.wsu.edu.
Yajuan LiuDepartment of Pathology, University of Washington, Seattle, Washington, 98195, USA. yajuan@uw.edu.
William S NobleDepartment of Genome Sciences, University of Washington, Seattle, Washington, 98195, USA. wnoble@uw.edu.
Jay ShendureDepartment of Genome Sciences, University of Washington, Seattle, Washington, 98195, USA. shendure@uw.edu.
Christine M DistecheDepartment of Pathology, University of Washington, Seattle, Washington, 98195, USA. cdistech@u.washington.edu.
University of Washington · USFred Hutch Cancer Center · USWashington State University · US

Funding

EDAC: ENCODE Data Analysis CenterU41HG007000 · NHGRI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WENG, ZHIPING · 2012 to 2016
$9.8M
Mouse X InactivationR01GM046883 · NIGMS · UNIVERSITY OF WASHINGTON · PI DISTECHE, CHRISTINE M. · 1992 to 2018
$5.9M
Modeling Mammalian GenomesR01GM098039 · NIGMS · UNIVERSITY OF WASHINGTON · PI BLAU, C. ANTHONY · 2011 to 2013
$1.8M
X-linked Genes, Histone Modifications, and BehaviorR01MH083949 · NIMH · WASHINGTON STATE UNIVERSITY · PI XU, JUN · 2010 to 2013
$1.6M
NHGRI NIH HHS U41 HG007000NIGMS NIH HHS GM046883NIGMS NIH HHS GM098039NIGMS NIH HHS R01 GM046883NIGMS NIH HHS R01 GM098039NIMH NIH HHS MH083949NIMH NIH HHS R01 MH083949
6 · The paper itself

Abstract

backgroundIn mammals, X chromosome genes are present in one copy in males and two in females. To balance the dosage of X-linked gene expression between the sexes, one of the X chromosomes in females is silenced. X inactivation is initiated by upregulation of the lncRNA (long non-coding RNA) Xist and recruitment of specific chromatin modifiers. The inactivated X chromosome becomes heterochromatic and visits a specific nuclear compartment adjacent to the nucleolus.

resultsHere, we show a novel role for the lncRNA Firre in anchoring the inactive mouse X chromosome and preserving one of its main epigenetic features, H3K27me3. Similar to Dxz4, Firre is X-linked and expressed from a macrosatellite repeat locus associated with a cluster of CTCF and cohesin binding sites, and is preferentially located adjacent to the nucleolus. CTCF binding present initially in both male and female mouse embryonic stem cells is lost from the active X during development. Knockdown of Firre disrupts perinucleolar targeting and H3K27me3 levels in mouse fibroblasts, demonstrating a role in maintenance of an important epigenetic feature of the inactive X chromosome. No X-linked gene reactivation is seen after Firre knockdown; however, a compensatory increase in the expression of chromatin modifier genes implicated in X silencing is observed. Further experiments in female embryonic stem cells suggest that Firre does not play a role in X inactivation onset.

conclusionsThe X-linked lncRNA Firre helps to position the inactive X chromosome near the nucleolus and to preserve one of its main epigenetic features.

Indexed as

AnimalsBinding SitesCCCTC-Binding FactorDNA MethylationFemaleJumonji Domain-Containing Histone DemethylasesMaleMicePromoter Regions, GeneticRepressor ProteinsRNA, Long NoncodingX ChromosomeX Chromosome InactivationCCCTC-Binding FactorCtcf protein, mouseFirre long non coding RNA, mouseJumonji Domain-Containing Histone DemethylasesKdm6b protein, mouseRepressor ProteinsRNA, Long Noncoding

Identifiers

PMID25887447
PMCPMC4391730
OpenAlexW2131306683

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.