Gravin-associated kinase signaling networks coordinate γ-tubulin organization at mitotic spindle poles

J Biol Chem. 2020 Oct 2;295(40):13784-13797. doi: 10.1074/jbc.RA120.014791. Epub 2020 Jul 30.

Abstract

Mitogenic signals that regulate cell division often proceed through multienzyme assemblies within defined intracellular compartments. The anchoring protein Gravin restricts the action of mitotic kinases and cell-cycle effectors to defined mitotic structures. In this report we discover that genetic deletion of Gravin disrupts proper accumulation and asymmetric distribution of γ-tubulin during mitosis. We utilize a new precision pharmacology tool, Local Kinase Inhibition, to inhibit the Gravin binding partner polo-like kinase 1 at spindle poles. Using a combination of gene-editing approaches, quantitative imaging, and biochemical assays, we provide evidence that disruption of local polo-like kinase 1 signaling underlies the γ-tubulin distribution defects observed with Gravin loss. Our study uncovers a new role for Gravin in coordinating γ-tubulin recruitment during mitosis and illuminates the mechanism by which signaling enzymes regulate this process at a distinct subcellular location.

Keywords: enzyme inhibitor; mitosis; protein complex; protein kinase; protein kinase A anchoring protein (AKAP); tubulin.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • A Kinase Anchor Proteins / genetics
  • A Kinase Anchor Proteins / metabolism*
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism*
  • HEK293 Cells
  • HeLa Cells
  • Humans
  • Polo-Like Kinase 1
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism*
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism*
  • Signal Transduction*
  • Spindle Apparatus / genetics
  • Spindle Apparatus / metabolism*
  • Tubulin / genetics
  • Tubulin / metabolism*

Substances

  • A Kinase Anchor Proteins
  • AKAP12 protein, human
  • Cell Cycle Proteins
  • Proto-Oncogene Proteins
  • TUBG1 protein, human
  • Tubulin
  • Protein Serine-Threonine Kinases