Evidence map›Paper›PMID 26151671›Full record

ArticleeLife2015

Mitotic fidelity requires transgenerational action of a testis-restricted HP1.

Mia T Levine, Helen M Vander Wende, Harmit S Malik

Abstract read
In one paragraph

Article in eLife, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Rapid evolution of a Y-chromosome heterochromatin protein underlies sex chromosome meiotic drive.Proceedings of the National Academy of Sciences of the United States of America · 2016
    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

3 authors.

Mia T LevineDivision of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, United States.
Helen M Vander WendeDivision of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, United States.
Harmit S MalikDivision of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, United States.ORCID http://orcid.org/0000-0001-6005-0016

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
Genetic Conflict Shapes Centromeres and HeterochromatinR01GM074108 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MALIK, HARMIT S. · 2005 to 2022
$6.1M
Evolutionary and functional diversification of chromatin proteinsR00GM107351 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI LEVINE, MIA TAUNA · 2015 to 2017
$727k
FHCRC High-Performance Computing ClusterS10OD020069 · OD · FRED HUTCHINSON CANCER RESEARCH CENTER · PI KOOPERBERG, CHARLES L · 2015 to 2015
$600k
Evolutionary and functional diversification of chromatin proteinsK99GM107351 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LEVINE, MIA TAUNA · 2013 to 2014
$180k
Phylogenomics and functional diversification of the Heterochromatin Protein 1 genF32GM097897 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LEVINE, MIA TAUNA · 2011 to 2012
$105k
Howard Hughes Medical InstituteNCI NIH HHS P30 CA015704NIGMS NIH HHS F32 GM097897NIGMS NIH HHS K99 GM107351NIGMS NIH HHS K99/R00 GM107351NIGMS NIH HHS R00 GM107351NIGMS NIH HHS R01 GM074108NIGMS NIH HHS R01 GM74108NIH HHS S10 OD020069
6 · The paper itself

Abstract

Sperm-packaged DNA must undergo extensive reorganization to ensure its timely participation in embryonic mitosis. Whereas maternal control over this remodeling is well described, paternal contributions are virtually unknown. In this study, we show that Drosophila melanogaster males lacking Heterochromatin Protein 1E (HP1E) sire inviable embryos that undergo catastrophic mitosis. In these embryos, the paternal genome fails to condense and resolve into sister chromatids in synchrony with the maternal genome. This delay leads to a failure of paternal chromosomes, particularly the heterochromatin-rich sex chromosomes, to separate on the first mitotic spindle. Remarkably, HP1E is not inherited on mature sperm chromatin. Instead, HP1E primes paternal chromosomes during spermatogenesis to ensure faithful segregation post-fertilization. This transgenerational effect suggests that maternal control is necessary but not sufficient for transforming sperm DNA into a mitotically competent pronucleus. Instead, paternal action during spermiogenesis exerts post-fertilization control to ensure faithful chromosome segregation in the embryo.

Indexed as

Chromosome SegregationMitosisAnimalsChromatinChromosomal Proteins, Non-HistoneDrosophila melanogasterDrosophila ProteinsMaleSpermatozoaTestisChromatinChromosomal Proteins, Non-HistoneDrosophila Proteinsheterochromatin protein 1, Drosophilacell biologychromosomesD. melanogastergenesheterochromatin proteinkaryotype evolutionmitosispaternal effect lethalsex chromosomesspermiogenesis

Identifiers

PMID26151671
PMCPMC4491702

What OpenQuestion holds

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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.