Evidence map›Paper›PMID 25785854›Full record

ArticlePLoS genetics2015

Escape from X inactivation varies in mouse tissues.

Joel B Berletch, Wenxiu Ma, Fan Yang, Jay Shendure, William S Noble, Christine M Disteche, Xinxian Deng

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 208 papers.

0numbers the graph read from it
0cells of the map it votes in
208citing papers in PubMed
18.5field-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

208 citing papers in PubMed, 309 citations in OpenAlex.

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148 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

7 authors at 1 institution in 1 country.

Joel B BerletchDepartment of Pathology, University of Washington, Seattle, Washington, United States of America.
Wenxiu MaDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Fan YangDepartment of Pathology, University of Washington, Seattle, Washington, United States of America.
Jay ShendureDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
William S NobleDepartment of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
Christine M DistecheDepartment of Pathology, University of Washington, Seattle, Washington, United States of America; Department of Medicine, University of Washington, Seattle, Washington, United States of America.
Xinxian DengDepartment of Pathology, University of Washington, Seattle, Washington, United States of America.
University of Washington · 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
Molecular studies of sex chromosome aneuploidyR01GM113943 · NIGMS · UNIVERSITY OF WASHINGTON · PI DISTECHE, CHRISTINE M. · 2015 to 2018
$1.7M
X-linked Genes, Histone Modifications, and BehaviorR01MH083949 · NIMH · WASHINGTON STATE UNIVERSITY · PI XU, JUN · 2010 to 2013
$1.6M
Mosaic Xlr3 Gene Expression in the Female Embryonic Mouse BrainR21MH099628 · NIMH · SEATTLE CHILDREN'S HOSPITAL · PI HEVNER, ROBERT F · 2013 to 2014
$537k
NHGRI NIH HHS U41 HG007000NIGMS NIH HHS GM046883NIGMS NIH HHS GM098039NIGMS NIH HHS R01 GM046883NIGMS NIH HHS R01 GM098039NIGMS NIH HHS R01 GM113943NIMH NIH HHS MH083949NIMH NIH HHS MH099628NIMH NIH HHS R01 MH083949NIMH NIH HHS R21 MH099628
6 · The paper itself

Abstract

X chromosome inactivation (XCI) silences most genes on one X chromosome in female mammals, but some genes escape XCI. To identify escape genes in vivo and to explore molecular mechanisms that regulate this process we analyzed the allele-specific expression and chromatin structure of X-linked genes in mouse tissues and cells with skewed XCI and distinguishable alleles based on single nucleotide polymorphisms. Using a binomial model to assess allelic expression, we demonstrate a continuum between complete silencing and expression from the inactive X (Xi). The validity of the RNA-seq approach was verified using RT-PCR with species-specific primers or Sanger sequencing. Both common escape genes and genes with significant differences in XCI status between tissues were identified. Such genes may be candidates for tissue-specific sex differences. Overall, few genes (3-7%) escape XCI in any of the mouse tissues examined, suggesting stringent silencing and escape controls. In contrast, an in vitro system represented by the embryonic-kidney-derived Patski cell line showed a higher density of escape genes (21%), representing both kidney-specific escape genes and cell-line specific escape genes. Allele-specific RNA polymerase II occupancy and DNase I hypersensitivity at the promoter of genes on the Xi correlated well with levels of escape, consistent with an open chromatin structure at escape genes. Allele-specific CTCF binding on the Xi clustered at escape genes and was denser in brain compared to the Patski cell line, possibly contributing to a more compartmentalized structure of the Xi and fewer escape genes in brain compared to the cell line where larger domains of escape were observed.

Indexed as

X Chromosome InactivationAnimalsCCCTC-Binding FactorDeoxyribonuclease IFemaleMiceOrgan SpecificityPolymorphism, Single NucleotideRepressor ProteinsRNA Polymerase IISequence Analysis, RNACCCTC-Binding FactorCtcf protein, mouseDeoxyribonuclease IRepressor ProteinsRNA Polymerase II

Identifiers

PMID25785854
PMCPMC4364777
OpenAlexW2076732852

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.