PKD controls mitotic Golgi complex fragmentation through a Raf-MEK1 pathway

Mol Biol Cell. 2013 Feb;24(3):222-33. doi: 10.1091/mbc.E12-03-0198. Epub 2012 Dec 14.

Abstract

Before entering mitosis, the stacks of the Golgi cisternae are separated from each other, and inhibiting this process delays entry of mammalian cells into mitosis. Protein kinase D (PKD) is known to be involved in Golgi-to-cell surface transport by controlling the biogenesis of specific transport carriers. Here we show that depletion of PKD1 and PKD2 proteins from HeLa cells by small interfering RNA leads to the accumulation of cells in the G2 phase of the cell cycle and prevents cells from entering mitosis. We further provide evidence that inhibition of PKD blocks mitotic Raf-1 and mitogen-activated protein kinase kinase (MEK) activation, and, as a consequence, mitotic Golgi fragmentation, which could be rescued by expression of active MEK1. Finally, Golgi fluorescence recovery after photobleaching analyses demonstrate that PKD is crucial for the cleavage of the noncompact zones of Golgi membranes in G2 phase. Our findings suggest that PKD controls interstack Golgi connections in a Raf-1/MEK1-dependent manner, a process required for entry of the cells into mitosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Fluorescence Recovery After Photobleaching
  • G2 Phase Cell Cycle Checkpoints
  • Gene Knockdown Techniques
  • Golgi Apparatus / metabolism*
  • HeLa Cells
  • Humans
  • Intracellular Membranes / metabolism
  • MAP Kinase Kinase 1 / metabolism*
  • Mitosis
  • Proto-Oncogene Proteins c-raf / metabolism*
  • RNA, Small Interfering / genetics
  • Signal Transduction
  • TRPP Cation Channels / genetics
  • TRPP Cation Channels / metabolism*

Substances

  • RNA, Small Interfering
  • TRPP Cation Channels
  • polycystic kidney disease 1 protein
  • polycystic kidney disease 2 protein
  • Proto-Oncogene Proteins c-raf
  • MAP Kinase Kinase 1
  • MAP2K1 protein, human