Evidence map›Paper›PMID 38943004›Full record

ArticleEMBO reports2024

Spermatocytes have the capacity to segregate chromosomes despite centriole duplication failure.

Marnie W Skinner, Carter J Simington, Pablo López-Jiménez, Kerstin A Baran, Jingwen Xu, Yaron Dayani, Marina V Pryzhkova, Jesús Page, Rocío Gómez, Andrew J Holland and 1 more

Abstract read
In one paragraph

Article in EMBO reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Therapeutic Repair of Sperm Quality Decline Caused by Polytetrafluoroethylene.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  10. Article
  11. 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

11 authors.

Marnie W SkinnerDepartment of Biochemistry and Molecular Biology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, USA.
Carter J SimingtonDepartment of Biochemistry and Molecular Biology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, USA.
Pablo López-JiménezDepartment of Biology, Autonomous University of Madrid, Madrid, Spain.ORCID 0000-0002-6673-5996
Kerstin A BaranDepartment of Biochemistry and Molecular Biology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, USA.
Jingwen XuDepartment of Biochemistry and Molecular Biology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, USA.ORCID 0009-0000-7306-3529
Yaron DayaniDepartment of Biochemistry and Molecular Biology, Uniformed Services University of the Health Sciences, Bethesda, MD, USA.
Marina V PryzhkovaDepartment of Biochemistry and Molecular Biology, Uniformed Services University of the Health Sciences, Bethesda, MD, USA.
Jesús PageDepartment of Biology, Autonomous University of Madrid, Madrid, Spain.
Rocío GómezDepartment of Biology, Autonomous University of Madrid, Madrid, Spain.ORCID 0000-0003-4408-9812
Andrew J HollandDepartment of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, MD, USA.ORCID 0000-0003-3728-6367
Philip W JordanDepartment of Biochemistry and Molecular Biology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, USA. philip.jordan@usuhs.edu.ORCID 0000-0003-4890-2647

Funding

TRAINING IN AREAS FUNDAMENTAL TO CANCER RESEARCHT32CA009110 · NCI · JOHNS HOPKINS UNIVERSITY · PI MATUNIS, MICHAEL J., WEERARATNA, ASHANI T · 1985 to 2025
$13.1M
Regulation of microtubule organizing centers during mammalian gametogenesisR01GM117155 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI Philip W Jordan · 2016 to 2026
$4.3M
Centrosome biogenesis and copy number controlR01GM114119 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI CORMACK, BRENDAN · 2015 to 2023
$3.3M
Pluripotent stem cell-derived organoid model of human gonad development, functions, and disordersR01HD114180 · NICHD · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI JORDAN, PHILIP W · 2023 to 2025
$1.7M
Regulation of Centrosome Biogenesis During Mammalian SpermatogenesisF31HD111265 · NICHD · JOHNS HOPKINS UNIVERSITY · PI SKINNER, MARNIE · 2023 to 2025
$115k
HHS | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) F31HD111265HHS | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) R01HD114180HHS | NIH | National Cancer Institute (NCI) CA009110HHS | NIH | National Institute of General Medical Sciences (NIGMS) R01GM11755NCI NIH HHS T32 CA009110NICHD NIH HHS F31 HD111265NICHD NIH HHS R01 HD114180NIGMS NIH HHS R01 GM114119NIGMS NIH HHS R01 GM117155
6 · The paper itself

Abstract

Centrosomes are the canonical microtubule organizing centers (MTOCs) of most mammalian cells, including spermatocytes. Centrosomes comprise a centriole pair within a structurally ordered and dynamic pericentriolar matrix (PCM). Unlike in mitosis, where centrioles duplicate once per cycle, centrioles undergo two rounds of duplication during spermatogenesis. The first duplication is during early meiotic prophase I, and the second is during interkinesis. Using mouse mutants and chemical inhibition, we have blocked centriole duplication during spermatogenesis and determined that non-centrosomal MTOCs (ncMTOCs) can mediate chromosome segregation. This mechanism is different from the acentriolar MTOCs that form bipolar spindles in oocytes, which require PCM components, including gamma-tubulin and CEP192. From an in-depth analysis, we identified six microtubule-associated proteins, TPX2, KIF11, NuMA, and CAMSAP1-3, that localized to the non-centrosomal MTOC. These factors contribute to a mechanism that ensures bipolar MTOC formation and chromosome segregation during spermatogenesis when centriole duplication fails. However, despite the successful completion of meiosis and round spermatid formation, centriole inheritance and PLK4 function are required for normal spermiogenesis and flagella assembly, which are critical to ensure fertility.

Indexed as

CentriolesChromosome SegregationMicrotubule-Associated ProteinsMicrotubule-Organizing CenterSpermatocytesSpermatogenesisAnimalsCell Cycle ProteinsMaleMeiosisMiceCell Cycle ProteinsMicrotubule-Associated ProteinsCentrioleCentrosomeMeiosisPLK4Spermatogenesis

Identifiers

PMID38943004
PMCPMC11316026

What OpenQuestion holds

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Registered trials

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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.