Sequential SNARE disassembly and GATE-16-GOS-28 complex assembly mediated by distinct NSF activities drives Golgi membrane fusion

J Cell Biol. 2002 Jun 24;157(7):1161-73. doi: 10.1083/jcb.200202082. Epub 2002 Jun 17.

Abstract

Characterization of mammalian NSF (G274E) and Drosophila NSF (comatose) mutants revealed an evolutionarily conserved NSF activity distinct from ATPase-dependent SNARE disassembly that was essential for Golgi membrane fusion. Analysis of mammalian NSF function during cell-free assembly of Golgi cisternae from mitotic Golgi fragments revealed that NSF disassembles Golgi SNAREs during mitotic Golgi fragmentation. A subsequent ATPase-independent NSF activity restricted to the reassembly phase is essential for membrane fusion. NSF/alpha-SNAP catalyze the binding of GATE-16 to GOS-28, a Golgi v-SNARE, in a manner that requires ATP but not ATP hydrolysis. GATE-16 is essential for NSF-driven Golgi reassembly and precludes GOS-28 from binding to its cognate t-SNARE, syntaxin-5. We suggest that this occurs at the inception of Golgi reassembly to protect the v-SNARE and regulate SNARE function.

Publication types

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

MeSH terms

  • Adenosine Triphosphatases / metabolism
  • Adenosine Triphosphatases / physiology*
  • Animals
  • Biological Transport, Active
  • CHO Cells
  • Carrier Proteins / physiology*
  • Cells, Cultured
  • Cricetinae
  • Drosophila
  • Evolution, Molecular
  • Golgi Apparatus / metabolism
  • Golgi Apparatus / physiology*
  • Intracellular Membranes / physiology*
  • Membrane Fusion / physiology*
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mitosis
  • Mutation
  • N-Ethylmaleimide-Sensitive Proteins
  • Recombinant Fusion Proteins / metabolism
  • SNARE Proteins
  • Vesicular Transport Proteins*

Substances

  • Carrier Proteins
  • Membrane Proteins
  • Recombinant Fusion Proteins
  • SNARE Proteins
  • Vesicular Transport Proteins
  • comt protein, Drosophila
  • Adenosine Triphosphatases
  • N-Ethylmaleimide-Sensitive Proteins