Microtubule-Driven Multimerization Recruits ase1p onto Overlapping Microtubules

L.C. Kapitein, M.E. Janson, S.M.J.L. van den Wildenberg, C.C. Hoogenraad, C.F. Schmidt, E.J.G. Peterman

Research output: Contribution to journalArticleAcademicpeer-review

62 Citations (Scopus)

Abstract

Microtubule (MT) crosslinking proteins of the ase1p/PRC1/Map65 family play a major role in the construction of MT networks such as the mitotic spindle. Most homologs in this family have been shown to localize with a remarkable specificity to sets of MTs that overlap with an antiparallel relative orientation []. Regulatory proteins bind to ase1p/PRC1/Map65 and appear to use the localization to set up precise spatial signals []. Here, we present evidence for a mechanism of localized protein multimerization underlying the specific targeting of ase1p, the fision yeast homolog. In controlled in vitro experiments, dimers of ase1-GFP diffused along the surface of single MTs and, at concentrations above a certain threshold, assembled into static multimeric structures. We observed that this threshold was significantly lower on overlapping MTs. We also observed diffusion and multimerization of ase1-GFP on MTs inside living cells, suggesting that a multimerization-driven localization mechanism is relevant in vivo. The domains responsible for MT binding and multimerization were identified via a series of ase1p truncations. Our findings show that cells use a finely tuned cooperative localization mechanism that exploits differences in the geometry and concentration of ase1p binding sites along single and overlapping MTs
Original languageEnglish
Pages (from-to)1713-1717
JournalCurrent Biology
Volume18
Issue number21
DOIs
Publication statusPublished - 2008

Keywords

  • fission yeast
  • midzone formation
  • cytokinesis
  • spindle
  • prc1
  • mitosis
  • arrays
  • roles
  • cells
  • kif4

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