Evidence map›Paper›PMID 24213375›Full record

ArticleNucleus (Austin, Tex.)

Histone variants and sensing of chromatin functional states.

Jérôme Govin, Saadi Khochbin

Open access · goldAbstract readComment
In one paragraph

Article in Nucleus (Austin, Tex.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Maternal histone variants and their chaperones promote paternal genome activation and boost somatic cell reprogramming.BioEssays : news and reviews in molecular, cellular and developmental biology · 2015
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 1 country.

Jérôme GovinCEA, iRTSV; Biologie à Grande Echelle; Grenoble, France; INSERM, U1038; Grenoble, France; Université Grenoble-Alpes; Grenoble, France; INSERM, U823; Institut Albert Bonniot; Grenoble, France.
Saadi KhochbinUniversité Grenoble-Alpes; Grenoble, France; INSERM, U823; Institut Albert Bonniot; Grenoble, France.
Institut de Recherches en Technologies et Sciences pour le Vivant · FRInstitut pour l'avancée des biosciences · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An extreme case of chromatin remodelling is the genome-wide exchange of histones with basic non-histone DNA-packaging proteins that occurs in post-meiotic male germ cells. The scale of this genome reorganization is such that chromatin needs to undergo a prior "preparation" for a facilitated action of the factors involved. Stage-specific incorporation of specialized histone variants, affecting large domains of chromatin, combined with histone post-translational modifications accompany the successive steps of the male genome reorganization. Recently, it has been shown that a testis-specific H2B variant, TH2B, one of the first identified core histone variants, replaces H2B at the time of cells' commitment into meiotic divisions and contributes to the process of global histone removal. These investigations also revealed a previously unknown histone dosage compensation mechanism that also ensures a functional interconnection between histone variant expression and histone post-translational modifications and will be further discussed here.

Indexed as

AnimalsChromatinFemaleHistonesMaleProtaminesChromatinHistonesProtaminesacetylationarginine methylationcrotonylationhistone chaperonehistone degradation

Identifiers

PMID24213375
PMCPMC3925688
OpenAlexW2109954394

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.