Evidence map›Paper›PMID 36727460›Full record

ArticleNucleic acids research2023

Species-specific regulation of XIST by the JPX/FTX orthologs.

Olga Rosspopoff, Emmanuel Cazottes, Christophe Huret, Agnese Loda, Amanda J Collier, Miguel Casanova, Peter J Rugg-Gunn, Edith Heard, Jean-François Ouimette, Claire Rougeulle

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
7.9field-weighted citation impact, top 2% 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

22 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
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  4. Remodeling ofScience advances · 2026
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  7. Review
  8. Genome research · 2025
    Article
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  14. Article
  15. Loss of XIST lncRNA unlocks stemness and cellular plasticity in ovarian cancer.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. Compensation of gene dosage on the mammalian X.Development (Cambridge, England) · 2024
    Review
  17. Review
  18. Review
  19. Review
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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

10 authors at 4 institutions in 3 countries.

Olga RosspopoffUniversité Paris Cité, CNRS, Epigenetics and Cell Fate, F-75013 Paris, France.
Emmanuel CazottesUniversité Paris Cité, CNRS, Epigenetics and Cell Fate, F-75013 Paris, France.
Christophe HuretUniversité Paris Cité, CNRS, Epigenetics and Cell Fate, F-75013 Paris, France.
Agnese LodaDirectors' research, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Amanda J CollierEpigenetics Programme, The Babraham Institute, Cambridge CB22 3AT, UK.
Miguel CasanovaUniversité Paris Cité, CNRS, Epigenetics and Cell Fate, F-75013 Paris, France.
Peter J Rugg-GunnEpigenetics Programme, The Babraham Institute, Cambridge CB22 3AT, UK.
Edith HeardDirectors' research, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Jean-François OuimetteUniversité Paris Cité, CNRS, Epigenetics and Cell Fate, F-75013 Paris, France.
Claire RougeulleUniversité Paris Cité, CNRS, Epigenetics and Cell Fate, F-75013 Paris, France.ORCID 0000-0003-3861-4940
Centre National de la Recherche Scientifique · FRBabraham Institute · GBCollège de France · FREuropean Molecular Biology Laboratory · DE

Funding

Medical Research Council MR/T011769/1Medical Research Council MR/V02969X/1
6 · The paper itself

Abstract

X chromosome inactivation (XCI) is an essential process, yet it initiates with remarkable diversity in various mammalian species. XIST, the main trigger of XCI, is controlled in the mouse by an interplay of lncRNA genes (LRGs), some of which evolved concomitantly to XIST and have orthologues across all placental mammals. Here, we addressed the functional conservation of human orthologues of two such LRGs, FTX and JPX. By combining analysis of single-cell RNA-seq data from early human embryogenesis with various functional assays in matched human and mouse pluripotent stem- or differentiated post-XCI cells, we demonstrate major functional differences for these orthologues between species, independently of primary sequence conservation. While the function of FTX is not conserved in humans, JPX stands as a major regulator of XIST expression in both species. However, we show that different entities of JPX control the production of XIST at various steps depending on the species. Altogether, our study highlights the functional versatility of LRGs across evolution, and reveals that functional conservation of orthologous LRGs may involve diversified mechanisms of action. These findings represent a striking example of how the evolvability of LRGs can provide adaptative flexibility to constrained gene regulatory networks.

Indexed as

PlacentaRNA, Long NoncodingAnimalsEmbryo, MammalianFemaleHumansMammalsMicePregnancyX Chromosome InactivationRNA, Long Noncoding

Identifiers

PMID36727460
PMCPMC10018341
OpenAlexW4318913945

What OpenQuestion holds

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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.