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.

Development (Cambridge, England)
|March 16, 2021
PubMed

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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