CP55, a novel key component of centrosomal organization in Dictyostelium

Cell Mol Life Sci. 2012 Nov;69(21):3651-64. doi: 10.1007/s00018-012-1040-3. Epub 2012 Jun 29.

Abstract

Dictyostelium centrosomes consist of a layered core structure surrounded by a microtubule-nucleating corona. At the G2/M transition, the corona dissociates and the core structure duplicates, yielding two spindle pole bodies. Finally, in telophase, the spindle poles mature into two new, complete centrosomes. CP55 was identified in a centrosomal proteome analysis. It is a component of the centrosomal core structure, and persists at the centrosome throughout the entire cell cycle. FRAP experiments revealed that during interphase the majority of centrosomal GFP-CP55 is immobile, which indicates a structural task of CP55 at the centrosome. The CP55null mutant is characterized by increased ploidy, a less structured, slightly enlarged corona, and by supernumerary, cytosolic MTOCs, containing only corona proteins and lacking a core structure. Live cell imaging showed that supernumerary MTOCs arise in telophase. Lack of CP55 also caused premature recruitment of the corona organizer CP148 to mitotic spindle poles, already in metaphase instead of telophase. Forces transmitted through astral microtubules may expel prematurely acquired or loosely attached corona fragments into the cytosol, where they act as independent MTOCs. CP55null cells were also impaired in growth, most probably due to difficulties in centrosome splitting during prophase. Furthermore, although they were still capable of phagocytosis, they appeared unable to utilize phagocytosed nutrients. This inability may be attributed to their partially disorganized Golgi apparatus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Division
  • Centrosome / metabolism*
  • Dictyostelium / cytology
  • Dictyostelium / genetics
  • Dictyostelium / metabolism*
  • Gene Knockout Techniques
  • Golgi Apparatus / metabolism
  • Interphase
  • Microtubule-Organizing Center / chemistry
  • Microtubule-Organizing Center / metabolism
  • Mitosis
  • Phagocytosis
  • Ploidies
  • Protozoan Proteins / genetics
  • Protozoan Proteins / metabolism*
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Spindle Apparatus / metabolism

Substances

  • Protozoan Proteins
  • Recombinant Proteins