Evidence map›Paper›PMID 28794128›Full record

ArticleThe Journal of cell biology2017

Dynamic changes in H1 subtype composition during epigenetic reprogramming.

Annalisa Izzo, Céline Ziegler-Birling, Peter W S Hill, Lydia Brondani, Petra Hajkova, Maria-Elena Torres-Padilla, Robert Schneider

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. The remodeling of Z-DNA in the mammalian germ line.Biochemical Society transactions · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Chromatin regulation and dynamics in stem cells.Current topics in developmental biology · 2020
    Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
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

7 authors at 3 institutions in 3 countries.

Annalisa IzzoInstitute of Functional Epigenetics, Helmholtz Zentrum München, Neuherberg, Germany.
Céline Ziegler-BirlingInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Université de Strasbourg, Illkirch, France.
Peter W S HillHammersmith Hospital Campus, Medical Research Council London Institute of Medical Sciences, London, England, UK.
Lydia BrondaniInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Université de Strasbourg, Illkirch, France.
Petra HajkovaHammersmith Hospital Campus, Medical Research Council London Institute of Medical Sciences, London, England, UK.ORCID 0000-0003-4145-1468
Maria-Elena Torres-PadillaInstitute of Epigenetics and Stem Cells, Helmholtz Zentrum München, Neuherberg, Germany torres-padilla@helmholtz-muenchen.de.
Robert SchneiderInstitute of Functional Epigenetics, Helmholtz Zentrum München, Neuherberg, Germany robert.schneider@helmholtz-muenchen.de.ORCID 0000-0001-5303-0973
Helmholtz Zentrum München · DEHammersmith Hospital · GBInstitut de génétique et de biologie moléculaire et cellulaire · FR

Funding

Medical Research Council MC_U120092689
6 · The paper itself

Abstract

In mammals, histone H1 consists of a family of related proteins, including five replication-dependent (H1.1-H1.5) and two replication-independent (H1.10 and H1.0) subtypes, all expressed in somatic cells. To systematically study the expression and function of H1 subtypes, we generated knockin mouse lines in which endogenous H1 subtypes are tagged. We focused on key developmental periods when epigenetic reprogramming occurs: early mouse embryos and primordial germ cell development. We found that dynamic changes in H1 subtype expression and localization are tightly linked with chromatin remodeling and might be crucial for transitions in chromatin structure during reprogramming. Although all somatic H1 subtypes are present in the blastocyst, each stage of preimplantation development is characterized by a different combination of H1 subtypes. Similarly, the relative abundance of somatic H1 subtypes can distinguish male and female chromatin upon sex differentiation in developing germ cells. Overall, our data provide new insights into the chromatin changes underlying epigenetic reprogramming. We suggest that distinct H1 subtypes may mediate the extensive chromatin remodeling occurring during epigenetic reprogramming and that they may be key players in the acquisition of cellular totipotency and the establishment of specific cellular states.

Identifiers

PMID28794128
PMCPMC5626532
OpenAlexW2742768644

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.