Rebuilding MTOCs upon centriole loss during mouse oogenesis

Dev Biol. 2013 Oct 1;382(1):48-56. doi: 10.1016/j.ydbio.2013.07.029. Epub 2013 Aug 14.

Abstract

The vast majority of animal cells contain canonical centrosomes as a main microtubule-organizing center defined by a central pair of centrioles. As a rare and striking exception to this rule, vertebrate oocytes loose their centrioles at an early step of oogenesis. At the end of oogenesis, centrosomes are eventually replaced by numerous acentriolar microtubule-organizing centers (MTOCs) that shape the spindle poles during meiotic divisions. The mechanisms involved in centrosome and acentriolar MTOCs metabolism in oocytes have not been elucidated yet. In addition, little is known about microtubule organization and its impact on intracellular architecture during the oocyte growth phase following centrosome disassembly. We have investigated this question in the mouse by coupling immunofluorescence and live-imaging approaches. We show that growing oocytes contain dispersed pericentriolar material, responsible for microtubule assembly and distribution all over the cell. The gradual enlargement of PCM foci eventually leads in competent oocytes to the formation of big perinuclear MTOCs and to the assembly of large microtubule asters emanating from the close vicinity of the nucleus. Upon meiosis resumption, perinuclear MTOCs spread around the nuclear envelope, which in parallel is remodelled before breaking-down, via a MT- and dynein-dependent mechanism. Only fully competent oocytes are able to perform this dramatic reorganization at NEBD. Therefore, the MTOC-MT reorganization that we describe is one of key feature of mouse oocyte competency.

Keywords: Acentriolar MTOC; Growth phase; Mouse; NEBD; Oogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Nucleus / metabolism
  • Cell Proliferation
  • Centrioles / metabolism*
  • Dyneins / metabolism
  • Female
  • Meiosis
  • Mice
  • Microtubule-Organizing Center / metabolism*
  • Microtubules / metabolism
  • Oocytes / cytology
  • Oocytes / metabolism
  • Oogenesis*

Substances

  • Dyneins