Evidence map›Paper›PMID 24795146›Full record

ArticleBiology open2014

H3K79 methylation: a new conserved mark that accompanies H4 hyperacetylation prior to histone-to-protamine transition in Drosophila and rat.

Christine Dottermusch-Heidel, Stefanie M K Gärtner, Isabel Tegeder, Christina Rathke, Bridlin Barckmann, Marek Bartkuhn, Sudhanshu Bhushan, Klaus Steger, Andreas Meinhardt, Renate Renkawitz-Pohl

Open access · goldAbstract read
In one paragraph

Article in Biology open, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  3. Article
  4. Article
  5. Review
  6. Connecting the DOTs on Cell Identity.Frontiers in cell and developmental biology · 2022
    Review
  7. Article
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  9. Article
  10. Review
  11. Article
  12. Article
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  14. Article
  15. Review
  16. Review
  17. Epigenetic regulation of germ cells-remember or forget?Current opinion in genetics & development · 2015
    Review
  18. Article
  19. 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

10 authors at 2 institutions in 1 country.

Christine Dottermusch-HeidelFachbereich Biologie, Entwicklungsbiologie, Philipps-Universität Marburg, Karl-von-Frisch Strasse 8, 35043 Marburg, Germany.
Stefanie M K GärtnerFachbereich Biologie, Entwicklungsbiologie, Philipps-Universität Marburg, Karl-von-Frisch Strasse 8, 35043 Marburg, Germany.
Isabel TegederFachbereich Biologie, Entwicklungsbiologie, Philipps-Universität Marburg, Karl-von-Frisch Strasse 8, 35043 Marburg, Germany.
Christina RathkeFachbereich Biologie, Entwicklungsbiologie, Philipps-Universität Marburg, Karl-von-Frisch Strasse 8, 35043 Marburg, Germany.
Bridlin BarckmannFachbereich Biologie, Entwicklungsbiologie, Philipps-Universität Marburg, Karl-von-Frisch Strasse 8, 35043 Marburg, Germany Present address: Institut de Génétique Humaine, CNRS UPR 1142, 141 Rue de la Cardonille, 34396, Montpellier Cedex 5, France.
Marek BartkuhnDepartment of Genetics, Justus Liebig University Giessen, Heinrich-Buff-Ring 58-62, 35392 Giessen, Germany.
Sudhanshu BhushanUnit of Reproductive Biology, Department of Anatomy and Cell Biology, Justus Liebig University Giessen, Aulweg 123, 35385 Giessen, Germany.
Klaus StegerMolecular Andrology Section, Department of Urology, Pediatric Urology and Andrology, Justus Liebig University Giessen, Schubertstrasse 81, 35392 Giessen, Germany.
Andreas MeinhardtUnit of Reproductive Biology, Department of Anatomy and Cell Biology, Justus Liebig University Giessen, Aulweg 123, 35385 Giessen, Germany.
Renate Renkawitz-PohlFachbereich Biologie, Entwicklungsbiologie, Philipps-Universität Marburg, Karl-von-Frisch Strasse 8, 35043 Marburg, Germany renkawit@biologie.uni-marburg.de.
Philipps University of Marburg · DEUniversity of Giessen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During spermiogenesis, haploid spermatids undergo extensive chromatin remodeling events in which histones are successively replaced by more basic protamines to generate highly compacted chromatin. Here we show for the first time that H3K79 methylation is a conserved feature preceding the histone-to-protamine transition in Drosophila melanogaster and rat. During Drosophila spermatogenesis, the Dot1-like methyltransferase Grappa (Gpp) is primarily expressed in canoe stage nuclei. The corresponding H3K79 methylation is a histone modification that precedes the histone-to-protamine transition and correlates with histone H4 hyperacetylation. When acetylation was inhibited in cultured Drosophila testes, nuclei were smaller and chromatin was compact, Gpp was little synthesized, H3K79 methylation was strongly reduced, and protamines were not synthesized. The Gpp isoform Gpp-D has a unique C-terminus, and Gpp is essential for full fertility. In rat, H3K79 methylation also correlates with H4 hyperacetylation but not with active RNA polymerase II, which might point towards a conserved function in chromatin remodeling during the histone-to-protamine transition in both Drosophila and rat.

Indexed as

GppGpp-DGrappaH4 acetylationHistone-to-protamine transitionSpermiogenesis

Identifiers

PMID24795146
PMCPMC4058078
OpenAlexW2136020785

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.