Glutamylation of centrosomes ensures their function by recruiting microtubule nucleation factors

EMBO J. 2025 May;44(10):2976-2996. doi: 10.1038/s44318-025-00435-y. Epub 2025 Apr 14.

Abstract

Centrosomes are tubulin-based organelles that undergo glutamylation, a post-translational modification that conjugates glutamic acid residues to tubulins. Although centrosomal glutamylation has been known for several decades, how this modification regulates centrosome structure and function remains unclear. To address this long-standing issue, we developed a method to spatiotemporally reduce centrosomal glutamylation by recruiting an engineered deglutamylase to centrosomes. We found that centrosome structure remains largely unaffected by centrosomal hypoglutamylation. Intriguingly, glutamylation physically recruits, via electrostatic forces, the NEDD1/CEP192/γ-tubulin complex to centrosomes, ensuring microtubule nucleation and proper trafficking of centriolar satellites. The consequent defect in centriolar satellite trafficking leads to reduced levels of the ciliogenesis factor Talpid3, suppressing ciliogenesis. Centrosome glutamylation also promotes proper mitotic spindle formation and mitosis. In summary, our study provides a new approach to spatiotemporally manipulate glutamylation at centrosomes, and offers novel insights into how centrosomes are organized and regulated by glutamylation.

Keywords: Centriolar satellites; Centrosomes; Glutamylation; Microtubules; Primary Cilia.

MeSH terms

  • Centrosome* / metabolism
  • Chromosomal Proteins, Non-Histone
  • HeLa Cells
  • Humans
  • Microtubule-Associated Proteins* / genetics
  • Microtubule-Associated Proteins* / metabolism
  • Microtubules* / metabolism
  • Mitosis
  • Protein Processing, Post-Translational*
  • Spindle Apparatus / metabolism
  • Tubulin / metabolism

Substances

  • Microtubule-Associated Proteins
  • Tubulin
  • NEDD1 protein, human
  • Cep192 protein, human
  • Chromosomal Proteins, Non-Histone