Reactivation of spindle elongation in vitro is correlated with the phosphorylation of a 205 kd spindle-associated protein

Cell. 1987 Aug 14;50(4):535-43. doi: 10.1016/0092-8674(87)90026-2.

Abstract

Mitotic spindles isolated from the diatom Stephanopyxis turris consist of two half-spindles of closely interdigitating microtubules that slide relative to one another in the presence of ATP, reinitiating spindle elongation (anaphase B) in vitro. Purified spindles that have been exposed to ATP-gamma-S undergo ATP-dependent reactivation more readily than do control spindles. Thiophosphorylated proteins in such spindles are located in the spindle midzone, kinetochores, and a portion of the pole complex. One major thiophosphorylated peptide of 205 kd is detected in extracts prepared from spindles labeled with [35S]ATP-gamma-S, and is also localized in the spindle midzone by using an antibody that recognizes thiophosphorylated proteins. It is likely that this 205 kd peptide is either a positive regulator or mechanochemical transducer of microtubule sliding when it is in a phosphorylated state.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Triphosphate / analogs & derivatives
  • Adenosine Triphosphate / metabolism
  • Anaphase*
  • Eukaryota / metabolism*
  • Eukaryota / ultrastructure
  • Fluorescent Antibody Technique
  • Microtubule-Associated Proteins / metabolism*
  • Phosphoric Monoester Hydrolases / antagonists & inhibitors
  • Phosphorylation
  • Spindle Apparatus / metabolism*

Substances

  • Microtubule-Associated Proteins
  • adenosine 5'-O-(3-thiotriphosphate)
  • Adenosine Triphosphate
  • Phosphoric Monoester Hydrolases