Evidence map›Paper›PMID 27857184›Full record

ArticleScientific reports2016

YY1 binding association with sex-biased transcription revealed through X-linked transcript levels and allelic binding analyses.

Chih-Yu Chen, Wenqiang Shi, Bradley P Balaton, Allison M Matthews, Yifeng Li, David J Arenillas, Anthony Mathelier, Masayoshi Itoh, Hideya Kawaji, Timo Lassmann and 5 more

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Defective Astrocyte Maturation Drives Cerebellar Neuroinflammation and Degeneration.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Satellite DNAs and human sex chromosome variation.Seminars in cell & developmental biology · 2022
    Review
  16. The Molecular and Nuclear Dynamics of X-Chromosome Inactivation.Cold Spring Harbor perspectives in biology · 2022
    Review
  17. Article
  18. Article
  19. Review
  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

15 authors.

Chih-Yu ChenCentre for Molecular Medicine and Therapeutics, Child and Family Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Wenqiang ShiCentre for Molecular Medicine and Therapeutics, Child and Family Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Bradley P BalatonDepartment of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
Allison M MatthewsCentre for Molecular Medicine and Therapeutics, Child and Family Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Yifeng LiCentre for Molecular Medicine and Therapeutics, Child and Family Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
David J ArenillasCentre for Molecular Medicine and Therapeutics, Child and Family Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Anthony MathelierCentre for Molecular Medicine and Therapeutics, Child and Family Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Masayoshi ItohRIKEN Omics Science Center, Yokohama, Japan.
Hideya KawajiRIKEN Omics Science Center, Yokohama, Japan.
Timo LassmannRIKEN Omics Science Center, Yokohama, Japan.
Yoshihide HayashizakiRIKEN Omics Science Center, Yokohama, Japan.
Piero CarninciRIKEN Omics Science Center, Yokohama, Japan.
Alistair R R ForrestRIKEN Omics Science Center, Yokohama, Japan.
Carolyn J BrownDepartment of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
Wyeth W WassermanCentre for Molecular Medicine and Therapeutics, Child and Family Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.

Funding

CIHR MOP-119586
6 · The paper itself

Abstract

Sex differences in susceptibility and progression have been reported in numerous diseases. Female cells have two copies of the X chromosome with X-chromosome inactivation imparting mono-allelic gene silencing for dosage compensation. However, a subset of genes, named escapees, escape silencing and are transcribed bi-allelically resulting in sexual dimorphism. Here we conducted in silico analyses of the sexes using human datasets to gain perspectives into such regulation. We identified transcription start sites of escapees (escTSSs) based on higher transcription levels in female cells using FANTOM5 CAGE data. Significant over-representations of YY1 transcription factor binding motif and ChIP-seq peaks around escTSSs highlighted its positive association with escapees. Furthermore, YY1 occupancy is significantly biased towards the inactive X (Xi) at long non-coding RNA loci that are frequent contacts of Xi-specific superloops. Our study suggests a role for YY1 in transcriptional activity on Xi in general through sequence-specific binding, and its involvement at superloop anchors.

Indexed as

Transcription, GeneticAllelesAllelic ImbalanceBinding SitesCell LineComputer SimulationFemaleGenes, X-LinkedHumansMaleProtein BindingRNA, Long NoncodingSex FactorsTranscription Initiation SiteX Chromosome InactivationYY1 Transcription FactorRNA, Long NoncodingXIST non-coding RNAYY1 Transcription Factor

Identifiers

PMID27857184
PMCPMC5114649

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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.