Evidence map›Paper›PMID 33964210›Full record

ArticleCell2021

Parental genome unification is highly error-prone in mammalian embryos.

Tommaso Cavazza, Yuko Takeda, Antonio Z Politi, Magomet Aushev, Patrick Aldag, Clara Baker, Meenakshi Choudhary, Jonas Bucevičius, Gražvydas Lukinavičius, Kay Elder and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 107 papers.

0numbers the graph read from it
0cells of the map it votes in
107citing papers in PubMed
28.1field-weighted citation impact, top 1% 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

107 citing papers in PubMed, 161 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Micronuclei: origins, assays, mechanisms, diseases and treatments.Signal transduction and targeted therapy · 2026
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. Article

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

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

15 authors at 5 institutions in 2 countries.

Tommaso CavazzaMax Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
Yuko TakedaWellcome Centre for Mitochondrial Research, Biosciences Institute, Newcastle University, NE1 4EP Newcastle upon Tyne, UK.
Antonio Z PolitiMax Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
Magomet AushevWellcome Centre for Mitochondrial Research, Biosciences Institute, Newcastle University, NE1 4EP Newcastle upon Tyne, UK.
Patrick AldagInstitute of Farm Animal Genetics, Biotechnology, Friedrich-Loeffler-Institute, Mariensee, 31535 Neustadt, Germany.
Clara BakerBourn Hall Clinic, CB23 2TN Cambridge, UK.
Meenakshi ChoudharyNewcastle Fertility Centre at Life, Newcastle upon Tyne Hospitals NHS Foundation Trust, NE1 4EP Newcastle upon Tyne, UK.
Jonas BucevičiusMax Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
Gražvydas LukinavičiusMax Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
Kay ElderBourn Hall Clinic, CB23 2TN Cambridge, UK.
Martyn BlayneyBourn Hall Clinic, CB23 2TN Cambridge, UK.
Andrea Lucas-HahnInstitute of Farm Animal Genetics, Biotechnology, Friedrich-Loeffler-Institute, Mariensee, 31535 Neustadt, Germany.
Heiner NiemannInstitute of Farm Animal Genetics, Biotechnology, Friedrich-Loeffler-Institute, Mariensee, 31535 Neustadt, Germany.
Mary HerbertWellcome Centre for Mitochondrial Research, Biosciences Institute, Newcastle University, NE1 4EP Newcastle upon Tyne, UK; Newcastle Fertility Centre at Life, Newcastle upon Tyne Hospitals NHS Foundation Trust, NE1 4EP Newcastle upon Tyne, UK.
Melina SchuhMax Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany. Electronic address: melina.schuh@mpibpc.mpg.de.
Max Planck Institute for Biophysical Chemistry · DEBourn Hall Clinic · GBFriedrich-Loeffler-Institut · DENewcastle upon Tyne Hospitals NHS Foundation Trust · GBWellcome Centre for Mitochondrial Research · GB

Funding

Wellcome 203105/Z/16/ZWellcome 215116/Z/18/ZWellcome Trust
6 · The paper itself

Abstract

Most human embryos are aneuploid. Aneuploidy frequently arises during the early mitotic divisions of the embryo, but its origin remains elusive. Human zygotes that cluster their nucleoli at the pronuclear interface are thought to be more likely to develop into healthy euploid embryos. Here, we show that the parental genomes cluster with nucleoli in each pronucleus within human and bovine zygotes, and clustering is required for the reliable unification of the parental genomes after fertilization. During migration of intact pronuclei, the parental genomes polarize toward each other in a process driven by centrosomes, dynein, microtubules, and nuclear pore complexes. The maternal and paternal chromosomes eventually cluster at the pronuclear interface, in direct proximity to each other, yet separated. Parental genome clustering ensures the rapid unification of the parental genomes on nuclear envelope breakdown. However, clustering often fails, leading to chromosome segregation errors and micronuclei, incompatible with healthy embryo development.

Indexed as

AneuploidyAnimalsCattleCell NucleolusCell NucleusCentrosomeChromosomesChromosome SegregationEmbryo, MammalianEmbryonic DevelopmentFertilizationHumansMaleMicrotubulesMitosisOocytesaneuploidycentrosomeschromosome segregationdyneinfertilizationgenome organizationhuman embryomicrotubulesnuclear pore complexspindle

Identifiers

PMID33964210
PMCPMC8162515
OpenAlexW3159677655

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.