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Updated: Jun 5, 2026

Multi-Photon Laser Ablation of Cytoplasmic Microtubule Organizing Centers in Mouse Oocytes
Published on: November 11, 2022
HURP permits MTOC sorting for robust meiotic spindle bipolarity, similar to extra centrosome clustering in cancer
Manuel Breuer1, Agnieszka Kolano, Mijung Kwon
1Unité Mixte de Recherche 7622, Centre National de la Recherche Scientifique/Université Pierre et Marie Curie, 75005 Paris, France.
Abstract:
In contrast to somatic cells, formation of acentriolar meiotic spindles relies on the organization of microtubules (MTs) and MT-organizing centers (MTOCs) into a stable bipolar structure. The underlying mechanisms are still unknown. We show that this process is impaired in hepatoma up-regulated protein (Hurp) knockout mice, which are viable but female sterile, showing defective oocyte divisions. HURP accumulates on interpolar MTs in the vicinity of chromosomes via Kinesin-5 activity. By promoting MT stability in the spindle central domain, HURP allows efficient MTOC sorting into distinct poles, providing bipolarity establishment and maintenance. Our results support a new model for meiotic spindle assembly in which HURP ensures assembly of a central MT array, which serves as a scaffold for the genesis of a robust bipolar structure supporting efficient chromosome congression. Furthermore, HURP is also required for the clustering of extra centrosomes before division, arguing for a shared molecular requirement of MTOC sorting in mammalian meiosis and cancer cell division.
Insights
Hepatoma up-regulated protein (Hurp) is crucial for organizing microtubule (MT) structures during female meiosis. Hurp ensures spindle bipolarity and chromosome alignment, essential for successful oocyte division and fertility.
Area of Science:
- Cell Biology
- Developmental Biology
- Genetics
Background:
- Acentric meiotic spindle formation requires organized microtubules (MTs) and MT-organizing centers (MTOCs) into a bipolar structure.
- The molecular mechanisms governing this process remain largely unknown.
Purpose of the Study:
- To investigate the role of Hepatoma Up-regulated protein (Hurp) in meiotic spindle assembly and oocyte division.
- To elucidate the mechanisms by which Hurp contributes to spindle bipolarity and chromosome congression.
Main Methods:
- Utilized hepatoma up-regulated protein (Hurp) knockout mice to study female sterility and defective oocyte divisions.
- Investigated the localization and function of HURP on interpolar MTs using Kinesin-5 activity.
Main Results:
- Hurp knockout mice exhibit impaired meiotic spindle formation and are female sterile.
- HURP accumulates on interpolar MTs near chromosomes, promoting MT stability in the spindle central domain.
- HURP facilitates efficient MTOC sorting for bipolarity establishment and maintenance, and clustering of extra centrosomes.
Conclusions:
- HURP is essential for meiotic spindle assembly, acting as a scaffold for a robust bipolar structure supporting chromosome congression.
- HURP plays a conserved role in MTOC sorting, crucial for both mammalian meiosis and cancer cell division.
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