Evidence map›Paper›PMID 30783652›Full record

ArticleNucleic acids research2019

En bloc and segmental deletions of human XIST reveal X chromosome inactivation-involving RNA elements.

Hyeon J Lee, Ramu Gopalappa, Hongjae Sunwoo, Seo-Won Choi, Suresh Ramakrishna, Jeannie T Lee, Hyongbum H Kim, Jin-Wu Nam

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. Xist in X chromosome inactivation: mechanisms and disease relevance.Cell communication and signaling : CCS · 2025
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Revisiting the consequences of deleting the X inactivation center.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  17. Article
  18. Article
  19. Biological Function of Long Non-coding RNA (LncRNA) Xist.Frontiers in cell and developmental biology · 2021
    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

8 authors at 3 institutions in 2 countries.

Hyeon J LeeDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 04763, Republic of Korea.
Ramu GopalappaDepartment of Pharmacology, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Hongjae SunwooDepartment of Molecular Biology, Massachusetts General Hospital, Department of Genetics, Harvard Medical School, Boston MA 02114, USA.
Seo-Won ChoiDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 04763, Republic of Korea.
Suresh RamakrishnaGraduate School of Biomedical Science and Engineering, Hanyang University, Seoul 04763, Republic of Korea.
Jeannie T LeeDepartment of Molecular Biology, Massachusetts General Hospital, Department of Genetics, Harvard Medical School, Boston MA 02114, USA.
Hyongbum H KimDepartment of Pharmacology, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Jin-Wu NamDepartment of Life Science, College of Natural Sciences, Hanyang University, Seoul 04763, Republic of Korea.
Hanyang University · KRHarvard University · USYonsei University · KR

Funding

TRAINING PROGRAM IN REPRODUCTIVE &DEVELOPMENTAL BIOLOGYT32HD007396 · NICHD · MASSACHUSETTS GENERAL HOSPITAL · PI CROWLEY, WILLIAM FRANCIS · 1991 to 2018
$2.5M
NICHD NIH HHS T32 HD007396
6 · The paper itself

Abstract

The XIST RNA is a non-coding RNA that induces X chromosome inactivation (XCI). Unlike the mouse Xist RNA, how the human XIST RNA controls XCI in female cells is less well characterized, and its functional motifs remain unclear. To systematically decipher the XCI-involving elements of XIST RNA, 11 smaller XIST segments, including repeats A, D and E; human-specific repeat elements; the promoter; and non-repetitive exons, as well as the entire XIST gene, were homozygously deleted in K562 cells using the Cas9 nuclease and paired guide RNAs at high efficiencies, followed by high-throughput RNA sequencing and RNA fluorescence in situ hybridization experiments. Clones containing en bloc and promoter deletions that consistently displayed no XIST RNAs and a global up-regulation of X-linked genes confirmed that the deletion of XIST reactivates the inactive X chromosome. Systematic analyses of segmental deletions delineated that exon 5 harboring the non-repeat element is important for X-inactivation maintenance, whereas exons 2, 3 and 4 as well as the other repeats in exon 1 are less important, a different situation from that of mouse Xist. This Cas9-assisted dissection of XIST allowed us to understand the unique functional domains within the human XIST RNA.

Indexed as

Base SequenceSequence DeletionX Chromosome InactivationAlternative SplicingAnimalsChromosomes, Human, XClone CellsCRISPR-Associated Protein 9CRISPR-Cas SystemsExonsGene EditingGenome, HumanHumansK562 CellsMicePromoter Regions, GeneticCRISPR-Associated Protein 9RNA, Guide, CRISPR-Cas SystemsRNA, Long NoncodingXIST non-coding RNA

Identifiers

PMID30783652
PMCPMC6486550
OpenAlexW2918088215

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.