Evidence map›Paper›PMID 26836306›Full record

ArticleeLife2016

Maternal LSD1/KDM1A is an essential regulator of chromatin and transcription landscapes during zygotic genome activation.

Katia Ancelin, Laurène Syx, Maud Borensztein, Noémie Ranisavljevic, Ivaylo Vassilev, Luis Briseño-Roa, Tao Liu, Eric Metzger, Nicolas Servant, Emmanuel Barillot and 3 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
9.9field-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

75 citing papers in PubMed, 127 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Exit from totipotency in mammals: an epigenetic perspective.Frontiers in cell and developmental biology · 2026
    Review
  6. Article
  7. Ectopic transcription due to inherited histone methylation may interfere with the ongoing function of differentiated neurons.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Review
  9. Review
  10. Article
  11. Mouse and human embryonic genome activation initiate at the one-cell stage.Frontiers in cell and developmental biology · 2025
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. H3K4me1 Modification Functions in Caste Differentiation in Honey Bees.International journal of molecular sciences · 2023
    Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Katia AncelinInstitut Curie, Paris, France.
Laurène SyxInstitut Curie, Paris, France.
Maud BorenszteinInstitut Curie, Paris, France.
Noémie RanisavljevicInstitut Curie, Paris, France.
Ivaylo VassilevInstitut Curie, Paris, France.
Luis Briseño-RoaHigh Fidelity Biology, Paris, France.
Tao LiuAnnoroad Gene Technology Co., Ltd, Beijing, China.
Eric MetzgerUrologische Klinik und Zentrale Klinische Forschung, Freiburg, Germany.
Nicolas ServantInstitut Curie, Paris, France.
Emmanuel BarillotInstitut Curie, Paris, France.
Chong-Jian ChenAnnoroad Gene Technology Co., Ltd, Beijing, China.
Roland SchüleUrologische Klinik und Zentrale Klinische Forschung, Freiburg, Germany.
Edith HeardInstitut Curie, Paris, France.ORCID http://orcid.org/0000-0001-8052-7117
Inserm · FRCentre National de la Recherche Scientifique · FRHôpital Saint-Michel · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Upon fertilization, the highly specialised sperm and oocyte genomes are remodelled to confer totipotency. The mechanisms of the dramatic reprogramming events that occur have remained unknown, and presumed roles of histone modifying enzymes are just starting to be elucidated. Here, we explore the function of the oocyte-inherited pool of a histone H3K4 and K9 demethylase, LSD1/KDM1A during early mouse development. KDM1A deficiency results in developmental arrest by the two-cell stage, accompanied by dramatic and stepwise alterations in H3K9 and H3K4 methylation patterns. At the transcriptional level, the switch of the maternal-to-zygotic transition fails to be induced properly and LINE-1 retrotransposons are not properly silenced. We propose that KDM1A plays critical roles in establishing the correct epigenetic landscape of the zygote upon fertilization, in preserving genome integrity and in initiating new patterns of genome expression that drive early mouse development.

Indexed as

Embryonic DevelopmentGene Expression Regulation, DevelopmentalTranscription, GeneticAnimalsChromatinEpigenesis, GeneticHistone DemethylasesMiceOocytesZygoteChromatinHistone DemethylasesKDM1a protein, mousechromosomesdevelopmental biologyepigenetic reprogramminggeneshistone demethylationlysine methylationmousepreimplantation developmentretrotransposonsstem cellstranscription regulation

Identifiers

PMID26836306
PMCPMC4829419
OpenAlexW2266984180

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.