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Updated: Nov 12, 2025

Meiotic Spindle Assessment in Mouse Oocytes by siRNA-mediated Silencing
Published on: October 11, 2015
Myosin-X is dispensable for spindle morphogenesis and positioning in the mouse oocyte
Flora Crozet1, Christelle Da Silva1, Marie-Hélène Verlhac1
1CIRB, Collège de France, UMR7241/U1050, 75005 Paris, France.
Abstract:
Off-center spindle positioning in mammalian oocytes enables asymmetric divisions in size, which are important for subsequent embryogenesis. The migration of the meiosis I spindle from the oocyte center to its cortex is mediated by F-actin. Specifically, an F-actin cage surrounds the microtubule spindle and applies forces to it. To better understand how F-actin transmits forces to the spindle, we studied a potential direct link between F-actin and microtubules. For this, we tested the implication of myosin-X, a known F-actin and microtubule binder involved in spindle morphogenesis and/or positioning in somatic cells, amphibian oocytes and embryos. Using a mouse strain conditionally invalidated for myosin-X in oocytes and by live-cell imaging, we show that myosin-X is not localized on the spindle, and is dispensable for spindle and F-actin assembly. It is not required for force transmission as spindle migration and chromosome alignment occur normally. More broadly, myosin-X is dispensable for oocyte developmental potential and female fertility. We therefore exclude a role for myosin-X in transmitting F-actin-mediated forces to the spindle, opening new perspectives regarding this mechanism in mouse oocytes, which differ from most mitotic cells.
Insights
Myosin-X is not essential for spindle positioning or force transmission in mouse oocytes, despite its known roles in other cells. This finding clarifies mechanisms of oocyte development and female fertility.
Area of Science:
- Cell Biology
- Developmental Biology
- Reproductive Biology
Background:
- Asymmetric cell division in mammalian oocytes is crucial for embryogenesis.
- F-actin mediates meiosis I spindle migration to the oocyte cortex.
- The precise mechanism of F-actin force transmission to the spindle is not fully understood.
Purpose of the Study:
- To investigate the role of myosin-X in F-actin-mediated spindle positioning in mouse oocytes.
- To determine if myosin-X directly links F-actin and microtubules for force transmission.
- To assess the necessity of myosin-X for oocyte developmental potential and female fertility.
Main Methods:
- Conditional inactivation of myosin-X in mouse oocytes.
- Live-cell imaging to observe spindle and F-actin dynamics.
- Analysis of spindle migration, chromosome alignment, and female fertility.
Main Results:
- Myosin-X was not localized to the spindle in mouse oocytes.
- Myosin-X was dispensable for spindle and F-actin assembly.
- Spindle migration, chromosome alignment, oocyte development, and female fertility were unaffected by myosin-X inactivation.
Conclusions:
- Myosin-X does not play a role in transmitting F-actin-mediated forces to the spindle in mouse oocytes.
- The mechanism of spindle positioning in mouse oocytes differs from that in most somatic cells.
- Further research is needed to elucidate the F-actin-microtubule interaction in mouse oocyte spindle positioning.
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