Evidence map›Paper›PMID 34107261›Full record

ArticleCell reports2021

Contiguous erosion of the inactive X in human pluripotency concludes with global DNA hypomethylation.

Prakhar Bansal, Darcy T Ahern, Yuvabharath Kondaveeti, Catherine W Qiu, Stefan F Pinter

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
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  12. Using Organoids to Model Sex Differences in the Human Brain.Biological psychiatry global open science · 2024
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Stem cell models of Angelman syndrome.Frontiers in cell and developmental biology · 2023
    Review
  18. Monosomy X in isogenic human iPSC-derived trophoblast model impacts expression modules preserved in human placenta.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  19. A lifelong duty: how Xist maintains the inactive X chromosome.Current opinion in genetics & development · 2022
    Review
  20. Review
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

5 authors at 2 institutions in 1 country.

Prakhar BansalGraduate Program in Genetics and Developmental Biology, UCONN Health, University of Connecticut, Farmington, CT, USA; Department of Genetics and Genome Sciences, UCONN Health, University of Connecticut, Farmington, CT, USA.
Darcy T AhernGraduate Program in Genetics and Developmental Biology, UCONN Health, University of Connecticut, Farmington, CT, USA; Department of Genetics and Genome Sciences, UCONN Health, University of Connecticut, Farmington, CT, USA.
Yuvabharath KondaveetiDepartment of Genetics and Genome Sciences, UCONN Health, University of Connecticut, Farmington, CT, USA.
Catherine W QiuDepartment of Genetics and Genome Sciences, UCONN Health, University of Connecticut, Farmington, CT, USA.
Stefan F PinterGraduate Program in Genetics and Developmental Biology, UCONN Health, University of Connecticut, Farmington, CT, USA; Department of Genetics and Genome Sciences, UCONN Health, University of Connecticut, Farmington, CT, USA; Institute for Systems Genomics, University of Connecticut, Farmington, CT, USA. Electronic address: spinter@uchc.edu.
UConn Health · USUniversity of Connecticut · US

Funding

Mechanisms of escaping X chromosome inactivation and translation to X-linked diseaseR35GM124926 · NIGMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI PINTER, STEFAN F. · 2017 to 2021
$2.0M
NIGMS NIH HHS R35 GM124926
6 · The paper itself

Abstract

Female human pluripotent stem cells (hPSCs) routinely undergo inactive X (Xi) erosion. This progressive loss of key repressive features follows the loss of XIST expression, the long non-coding RNA driving X inactivation, and causes reactivation of silenced genes across the eroding X (Xe). To date, the sporadic and progressive nature of erosion has obscured its scale, dynamics, and key transition events. To address this problem, we perform an integrated analysis of DNA methylation (DNAme), chromatin accessibility, and gene expression across hundreds of hPSC samples. Differential DNAme orders female hPSCs across a trajectory from initiation to terminal Xi erosion. Our results identify a cis-regulatory element crucial for XIST expression, trace contiguously growing reactivated domains to a few euchromatic origins, and indicate that the late-stage Xe impairs DNAme genome-wide. Surprisingly, from this altered regulatory landscape emerge select features of naive pluripotency, suggesting that its link to X dosage may be partially conserved in human embryonic development.

Indexed as

Cell DifferentiationDNA MethylationFemaleHumansPluripotent Stem CellsX Chromosome Inactivationchromatin accessibilityDNA methylationescapee genesexpressiongene dosagehuman endogenous retroviral elementsnaive pluripotencyprimed pluripotencyX chromosomeXIST

Identifiers

PMID34107261
PMCPMC8267460
OpenAlexW3167061373

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.