Evidence map›Paper›PMID 26248554›Full record

ArticleGenome biology2015

Bipartite structure of the inactive mouse X chromosome.

Xinxian Deng, Wenxiu Ma, Vijay Ramani, Andrew Hill, Fan Yang, Ferhat Ay, Joel B Berletch, Carl Anthony Blau, Jay Shendure, Zhijun Duan and 2 more

Open access · goldAbstract 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 161 papers.

0numbers the graph read from it
0cells of the map it votes in
161citing papers in PubMed
23.5field-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

161 citing papers in PubMed, 273 citations in OpenAlex.

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101 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 1 institution in 1 country.

Xinxian DengDepartment of Pathology, University of Washington, Seattle, Washington, USA.
Wenxiu MaDepartment of Genome Sciences, University of Washington, Seattle, Washington, USA.
Vijay RamaniDepartment of Genome Sciences, University of Washington, Seattle, Washington, USA.
Andrew HillDepartment of Genome Sciences, University of Washington, Seattle, Washington, USA.
Fan YangDepartment of Pathology, University of Washington, Seattle, Washington, USA.
Ferhat AyDepartment of Genome Sciences, University of Washington, Seattle, Washington, USA.
Joel B BerletchDepartment of Pathology, University of Washington, Seattle, Washington, USA.
Carl Anthony BlauInstitute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, Washington, USA.
Jay ShendureDepartment of Genome Sciences, University of Washington, Seattle, Washington, USA.
Zhijun DuanInstitute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, Washington, USA. zjduan@uw.edu.
William S NobleDepartment of Genome Sciences, University of Washington, Seattle, Washington, USA. william-noble@uw.edu.
Christine M DistecheDepartment of Pathology, University of Washington, Seattle, Washington, USA. cdistech@u.washington.edu.
University of Washington · US

Funding

INTERDISCIPLINARY TRAINING IN GENOMIC SCIENCEST32HG000035 · NHGRI · UNIVERSITY OF WASHINGTON · PI Bruce Colston Trapnell · 1995 to 2026
$24.2M
Mouse X InactivationR01GM046883 · NIGMS · UNIVERSITY OF WASHINGTON · PI DISTECHE, CHRISTINE M. · 1992 to 2018
$5.9M
Massively Parallel Contiguity MappingR01HG006283 · NHGRI · UNIVERSITY OF WASHINGTON · PI SHENDURE, JAY ASHOK · 2011 to 2016
$3.4M
Modeling Mammalian GenomesR01GM098039 · NIGMS · UNIVERSITY OF WASHINGTON · PI BLAU, C. ANTHONY · 2011 to 2013
$1.8M
NHGRI NIH HHS R01 HG006283NHGRI NIH HHS T32 HG000035NIGMS NIH HHS GM046883NIGMS NIH HHS GM098039NIGMS NIH HHS R01 GM046883NIGMS NIH HHS R01 GM098039
6 · The paper itself

Abstract

backgroundIn mammals, one of the female X chromosomes and all imprinted genes are expressed exclusively from a single allele in somatic cells. To evaluate structural changes associated with allelic silencing, we have applied a recently developed Hi-C assay that uses DNase I for chromatin fragmentation to mouse F1 hybrid systems.

resultsWe find radically different conformations for the two female mouse X chromosomes. The inactive X has two superdomains of frequent intrachromosomal contacts separated by a boundary region. Comparison with the recently reported two-superdomain structure of the human inactive X shows that the genomic content of the superdomains differs between species, but part of the boundary region is conserved and located near the Dxz4/DXZ4 locus. In mouse, the boundary region also contains a minisatellite, Ds-TR, and both Dxz4 and Ds-TR appear to be anchored to the nucleolus. Genes that escape X inactivation do not cluster but are located near the periphery of the 3D structure, as are regions enriched in CTCF or RNA polymerase. Fewer short-range intrachromosomal contacts are detected for the inactive alleles of genes subject to X inactivation compared with the active alleles and with genes that escape X inactivation. This pattern is also evident for imprinted genes, in which more chromatin contacts are detected for the expressed allele.

conclusionsBy applying a novel Hi-C method to map allelic chromatin contacts, we discover a specific bipartite organization of the mouse inactive X chromosome that probably plays an important role in maintenance of gene silencing.

Indexed as

X Chromosome InactivationAnimalsCCCTC-Binding FactorCell LineCell NucleolusCells, CulturedChromosomes, Human, XFemaleGenomic ImprintingHumansMaleMiceRepressor ProteinsRNA Polymerase IIX ChromosomeCCCTC-Binding FactorCTCF protein, humanCtcf protein, mouseRepressor ProteinsRNA Polymerase II

Identifiers

PMID26248554
PMCPMC4539712
OpenAlexW1783209592

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.