Evidence map›Paper›PMID 28923964›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Repeat E anchors Xist RNA to the inactive X chromosomal compartment through CDKN1A-interacting protein (CIZ1).

Hongjae Sunwoo, David Colognori, John E Froberg, Yesu Jeon, Jeannie T Lee

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
12.8field-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

84 citing papers in PubMed, 143 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Xist in X chromosome inactivation: mechanisms and disease relevance.Cell communication and signaling : CCS · 2025
    Review
  11. Article
  12. Review
  13. Review
  14. eLife · 2025
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

24 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

5 authors at 1 institution in 1 country.

Hongjae SunwooHoward Hughes Medical Institute, Massachusetts General Hospital, Boston, MA 02114.ORCID 0000-0001-8321-6269
David ColognoriHoward Hughes Medical Institute, Massachusetts General Hospital, Boston, MA 02114.
John E FrobergHoward Hughes Medical Institute, Massachusetts General Hospital, Boston, MA 02114.
Yesu JeonHoward Hughes Medical Institute, Massachusetts General Hospital, Boston, MA 02114.
Jeannie T LeeHoward Hughes Medical Institute, Massachusetts General Hospital, Boston, MA 02114; lee@molbio.mgh.harvard.edu.
Howard Hughes Medical Institute · US

Funding

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
Howard Hughes Medical InstituteNIGMS NIH HHS R01 GM090278
6 · The paper itself

Abstract

X chromosome inactivation is an epigenetic dosage compensation mechanism in female mammals driven by the long noncoding RNA, Xist. Although recent genomic and proteomic approaches have provided a more global view of Xist's function, how Xist RNA localizes to the inactive X chromosome (Xi) and spreads in cis remains unclear. Here, we report that the CDKN1-interacting zinc finger protein CIZ1 is critical for localization of Xist RNA to the Xi chromosome territory. Stochastic optical reconstruction microscopy (STORM) shows a tight association of CIZ1 with Xist RNA at the single-molecule level. CIZ1 interacts with a specific region within Xist exon 7-namely, the highly repetitive Repeat E motif. Using genetic analysis, we show that loss of CIZ1 or deletion of Repeat E in female cells phenocopies one another in causing Xist RNA to delocalize from the Xi and disperse into the nucleoplasm. Interestingly, this interaction is exquisitely sensitive to CIZ1 levels, as overexpression of CIZ1 likewise results in Xist delocalization. As a consequence, this delocalization is accompanied by a decrease in H3K27me3 on the Xi. Our data reveal that CIZ1 plays a major role in ensuring stable association of Xist RNA within the Xi territory.

Indexed as

Chromosomes, MammalianNuclear ProteinsRepetitive Sequences, Nucleic AcidRNA, Long NoncodingX ChromosomeAnimalsFemaleGene Expression RegulationMiceMouse Embryonic Stem CellsNucleotide MotifsCiz1 protein, mouseNuclear ProteinsRNA, Long NoncodingXIST non-coding RNACIZ1noncoding RNARepeat EX inactivationXist

Identifiers

PMID28923964
PMCPMC5635913
OpenAlexW2754312617

What OpenQuestion holds

Textmetadata
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.