Polyglutamylated Tubulin Binding Protein C1orf96/CSAP Is Involved in Microtubule Stabilization in Mitotic Spindles

PLoS One. 2015 Nov 12;10(11):e0142798. doi: 10.1371/journal.pone.0142798. eCollection 2015.

Abstract

The centrosome-associated C1orf96/Centriole, Cilia and Spindle-Associated Protein (CSAP) targets polyglutamylated tubulin in mitotic microtubules (MTs). Loss of CSAP causes critical defects in brain development; however, it is unclear how CSAP association with MTs affects mitosis progression. In this study, we explored the molecular mechanisms of the interaction of CSAP with mitotic spindles. Loss of CSAP caused MT instability in mitotic spindles and resulted in mislocalization of Nuclear protein that associates with the Mitotic Apparatus (NuMA), with defective MT dynamics. Thus, CSAP overload in the spindles caused extensive MT stabilization and recruitment of NuMA. Moreover, MT stabilization by CSAP led to high levels of polyglutamylation on MTs. MT depolymerization by cold or nocodazole treatment was inhibited by CSAP binding. Live-cell imaging analysis suggested that CSAP-dependent MT-stabilization led to centrosome-free MT aster formation immediately upon nuclear envelope breakdown without γ-tubulin. We therefore propose that CSAP associates with MTs around centrosomes to stabilize MTs during mitosis, ensuring proper bipolar spindle formation and maintenance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Nuclear / metabolism
  • Cell Cycle Proteins
  • Cell Line
  • Centrioles / metabolism*
  • Centrioles / ultrastructure
  • HeLa Cells
  • Homeodomain Proteins / metabolism*
  • Humans
  • Microtubules / metabolism*
  • Microtubules / ultrastructure
  • Mitosis
  • Nuclear Matrix-Associated Proteins / metabolism
  • Nuclear Proteins / metabolism*
  • Polyglutamic Acid / metabolism
  • Repressor Proteins / metabolism*
  • Spindle Apparatus / metabolism*
  • Spindle Apparatus / ultrastructure
  • Transcription Factors
  • Tubulin / metabolism

Substances

  • Antigens, Nuclear
  • CUX1 protein, human
  • Cell Cycle Proteins
  • Homeodomain Proteins
  • NUMA1 protein, human
  • Nuclear Matrix-Associated Proteins
  • Nuclear Proteins
  • Repressor Proteins
  • Transcription Factors
  • Tubulin
  • Polyglutamic Acid

Grants and funding

Support was provided by: Japan Society for the Promotion of Science KAKENHI [grant Number 25870487, http://www.jsps.go.jp/english/e-grants/index.html] for the study design and preparation of the manuscript; The Nakajima foundation [http://www.nakajimafound.or.jp] for data collection and analysis; Takeda Science Foundation [http://www.takeda-sci.or.jp] for data collection and analysis; The Kanae Foundation for the Promotion of Medical Science [http://www.kanae-zaidan.com/index.html] for data collection and analysis.