Evidence map›Paper›PMID 24162848›Full record

ArticleNature2013

High-resolution Xist binding maps reveal two-step spreading during X-chromosome inactivation.

Matthew D Simon, Stefan F Pinter, Rui Fang, Kavitha Sarma, Michael Rutenberg-Schoenberg, Sarah K Bowman, Barry A Kesner, Verena K Maier, Robert E Kingston, Jeannie T Lee

Open access · greenAbstract read
In one paragraph

Article in Nature, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 246 papers.

0numbers the graph read from it
0cells of the map it votes in
246citing papers in PubMed
29.0field-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

246 citing papers in PubMed, 399 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. eLife · 2025
    Article
  16. Article
  17. Re-analysis of CLAP data affirms PRC2 as an RNA binding protein.bioRxiv : the preprint server for biology · 2025
    Article
  18. Article
  19. Article
  20. Article

186 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Matthew D Simon *Department of Molecular Biology, Massachusetts General Hospital, and Department of Genetics, Harvard Medical School, Boston, MA 02114.
Stefan F Pinter *Department of Molecular Biology, Massachusetts General Hospital, and Department of Genetics, Harvard Medical School, Boston, MA 02114.
Rui Fang *Dept. of Molecular Biophysics and Biochemistry, and Chemical Biology Institute, Yale University, West Haven, CT, 06516.
Kavitha SarmaDepartment of Molecular Biology, Massachusetts General Hospital, and Department of Genetics, Harvard Medical School, Boston, MA 02114.
Michael Rutenberg-SchoenbergDept. of Molecular Biophysics and Biochemistry, and Chemical Biology Institute, Yale University, West Haven, CT, 06516.
Sarah K BowmanDepartment of Molecular Biology, Massachusetts General Hospital, and Department of Genetics, Harvard Medical School, Boston, MA 02114.
Barry A KesnerDepartment of Molecular Biology, Massachusetts General Hospital, and Department of Genetics, Harvard Medical School, Boston, MA 02114.
Verena K MaierDepartment of Molecular Biology, Massachusetts General Hospital, and Department of Genetics, Harvard Medical School, Boston, MA 02114.
Robert E KingstonDepartment of Molecular Biology, Massachusetts General Hospital, and Department of Genetics, Harvard Medical School, Boston, MA 02114.
Jeannie T LeeDepartment of Molecular Biology, Massachusetts General Hospital, and Department of Genetics, Harvard Medical School, Boston, MA 02114.
Howard Hughes Medical Institute · USMassachusetts General Hospital · USHarvard University · US

Funding

Skill Development for Diverse Scientific Careers: A New Course Predoctoral Program in Cellular and Molecular BiologyT32GM007223 · NIGMS · YALE UNIVERSITY · PI BASERGA, SUSAN J · 1985 to 2019
$31.0M
Maintenance of Gene ExpressionR01GM043901 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI KINGSTON, ROBERT · 1991 to 2018
$10.7M
Polycomb complexes targeted to specific loci by non-coding RNA co-factorsR01GM090278 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI LEE, JEANNIE T · 2010 to 2017
$3.7M
Deciphering the Role of MacroH2A in Non-coding RNA Mediated SilencingF32GM090765 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI SARMA, KAVITHA · 2010 to 2011
$99k
Howard Hughes Medical InstituteNIGMS NIH HHS F32 GM090765NIGMS NIH HHS F32-GM090765NIGMS NIH HHS R01 GM043901NIGMS NIH HHS R01-GM043901NIGMS NIH HHS R01 GM090278NIGMS NIH HHS R01-GM090278NIGMS NIH HHS T32 GM007223
6 · The paper itself

Abstract

The Xist long noncoding RNA (lncRNA) is essential for X-chromosome inactivation (XCI), the process by which mammals compensate for unequal numbers of sex chromosomes. During XCI, Xist coats the future inactive X chromosome (Xi) and recruits Polycomb repressive complex 2 (PRC2) to the X-inactivation centre (Xic). How Xist spreads silencing on a 150-megabases scale is unclear. Here we generate high-resolution maps of Xist binding on the X chromosome across a developmental time course using CHART-seq. In female cells undergoing XCI de novo, Xist follows a two-step mechanism, initially targeting gene-rich islands before spreading to intervening gene-poor domains. Xist is depleted from genes that escape XCI but may concentrate near escapee boundaries. Xist binding is linearly proportional to PRC2 density and H3 lysine 27 trimethylation (H3K27me3), indicating co-migration of Xist and PRC2. Interestingly, when Xist is acutely stripped off from the Xi in post-XCI cells, Xist recovers quickly within both gene-rich and gene-poor domains on a timescale of hours instead of days, indicating a previously primed Xi chromatin state. We conclude that Xist spreading takes distinct stage-specific forms. During initial establishment, Xist follows a two-step mechanism, but during maintenance, Xist spreads rapidly to both gene-rich and gene-poor regions.

Indexed as

X Chromosome InactivationAnimalsChromatinEmbryonic Stem CellsFemaleFibroblastsGenesGene SilencingHistone-Lysine N-MethyltransferaseHistonesLysineMethylationMiceModels, GeneticRNA, Long NoncodingX ChromosomeChromatinHistone-Lysine N-MethyltransferaseHistonesLysineRNA, Long NoncodingXIST non-coding RNA

Identifiers

PMID24162848
PMCPMC3904790
OpenAlexW1972717887

What OpenQuestion holds

Textmetadata
LicenceTDM
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.