NuMA is a mitotic adaptor protein that activates dynein and connects it to microtubule minus ends

J Cell Biol. 2025 Apr 7;224(4):e202408118. doi: 10.1083/jcb.202408118. Epub 2025 Feb 11.

Abstract

Nuclear mitotic apparatus protein (NuMA) is indispensable for the mitotic functions of the major microtubule minus-end directed motor cytoplasmic dynein 1. NuMA and dynein are both essential for correct spindle pole organization. How these proteins cooperate to gather microtubule minus ends at spindle poles remains unclear. Here, we use microscopy-based in vitro reconstitutions to demonstrate that NuMA is a dynein adaptor, activating processive dynein motility together with dynein's cofactors dynactin and Lissencephaly-1 (Lis1). Additionally, we find that NuMA binds and stabilizes microtubule minus ends, allowing dynein/dynactin/NuMA to transport microtubule minus ends as cargo to other minus ends. We further show that the microtubule-nucleating γ-tubulin ring complex (γTuRC) hinders NuMA binding and that NuMA only caps minus ends of γTuRC-nucleated microtubules after γTuRC release. These results provide new mechanistic insight into how dynein, dynactin, NuMA, and Lis1 together with γTuRC and uncapping proteins cooperate to organize spindle poles in cells.

MeSH terms

  • 1-Alkyl-2-acetylglycerophosphocholine Esterase / genetics
  • 1-Alkyl-2-acetylglycerophosphocholine Esterase / metabolism
  • Antigens, Nuclear / genetics
  • Antigens, Nuclear / metabolism
  • Cell Cycle Proteins* / genetics
  • Cell Cycle Proteins* / metabolism
  • Dynactin Complex* / genetics
  • Dynactin Complex* / metabolism
  • Dyneins* / genetics
  • Dyneins* / metabolism
  • HeLa Cells
  • Humans
  • Microtubule-Associated Proteins* / genetics
  • Microtubule-Associated Proteins* / metabolism
  • Microtubules* / metabolism
  • Mitosis*
  • Nuclear Matrix-Associated Proteins* / genetics
  • Nuclear Matrix-Associated Proteins* / metabolism
  • Protein Binding
  • Spindle Apparatus / genetics
  • Spindle Apparatus / metabolism
  • Spindle Poles / metabolism
  • Tubulin / metabolism

Substances

  • Dynactin Complex
  • NUMA1 protein, human
  • Dyneins
  • Microtubule-Associated Proteins
  • Cell Cycle Proteins
  • Nuclear Matrix-Associated Proteins
  • PAFAH1B1 protein, human
  • 1-Alkyl-2-acetylglycerophosphocholine Esterase
  • Antigens, Nuclear
  • Tubulin