Rab6 regulates both ZW10/RINT-1 and conserved oligomeric Golgi complex-dependent Golgi trafficking and homeostasis

Mol Biol Cell. 2007 Oct;18(10):4129-42. doi: 10.1091/mbc.e07-01-0080. Epub 2007 Aug 15.

Abstract

We used multiple approaches to investigate the role of Rab6 relative to Zeste White 10 (ZW10), a mitotic checkpoint protein implicated in Golgi/endoplasmic reticulum (ER) trafficking/transport, and conserved oligomeric Golgi (COG) complex, a putative tether in retrograde, intra-Golgi trafficking. ZW10 depletion resulted in a central, disconnected cluster of Golgi elements and inhibition of ERGIC53 and Golgi enzyme recycling to ER. Small interfering RNA (siRNA) against RINT-1, a protein linker between ZW10 and the ER soluble N-ethylmaleimide-sensitive factor attachment protein receptor, syntaxin 18, produced similar Golgi disruption. COG3 depletion fragmented the Golgi and produced vesicles; vesicle formation was unaffected by codepletion of ZW10 along with COG, suggesting ZW10 and COG act separately. Rab6 depletion did not significantly affect Golgi ribbon organization. Epistatic depletion of Rab6 inhibited the Golgi-disruptive effects of ZW10/RINT-1 siRNA or COG inactivation by siRNA or antibodies. Dominant-negative expression of guanosine diphosphate-Rab6 suppressed ZW10 knockdown induced-Golgi disruption. No cross-talk was observed between Rab6 and endosomal Rab5, and Rab6 depletion failed to suppress p115 (anterograde tether) knockdown-induced Golgi disruption. Dominant-negative expression of a C-terminal fragment of Bicaudal D, a linker between Rab6 and dynactin/dynein, suppressed ZW10, but not COG, knockdown-induced Golgi disruption. We conclude that Rab6 regulates distinct Golgi trafficking pathways involving two separate protein complexes: ZW10/RINT-1 and COG.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adaptor Proteins, Vesicular Transport / metabolism
  • Cell Cycle Proteins / metabolism*
  • Chromosomal Proteins, Non-Histone / deficiency
  • Chromosomal Proteins, Non-Histone / metabolism*
  • Endocytosis
  • Endoplasmic Reticulum / metabolism
  • Golgi Apparatus / metabolism*
  • Golgi Matrix Proteins
  • HeLa Cells
  • Homeostasis*
  • Humans
  • Membrane Proteins / metabolism
  • Microtubule-Associated Proteins / deficiency
  • Microtubule-Associated Proteins / metabolism*
  • Models, Biological
  • Molecular Motor Proteins / metabolism
  • Multiprotein Complexes / metabolism*
  • Protein Transport
  • RNA, Small Interfering / metabolism
  • Vesicular Transport Proteins / metabolism
  • rab GTP-Binding Proteins / deficiency
  • rab GTP-Binding Proteins / metabolism*

Substances

  • Adaptor Proteins, Vesicular Transport
  • COG3 protein, human
  • Cell Cycle Proteins
  • Chromosomal Proteins, Non-Histone
  • Golgi Matrix Proteins
  • Membrane Proteins
  • Microtubule-Associated Proteins
  • Molecular Motor Proteins
  • Multiprotein Complexes
  • RINT1 protein, human
  • RNA, Small Interfering
  • Rab6 protein
  • Vesicular Transport Proteins
  • ZW10 protein, human
  • vesicular transport factor p115
  • rab GTP-Binding Proteins