C. elegans dynamin-related protein DRP-1 controls severing of the mitochondrial outer membrane

Mol Cell. 1999 Nov;4(5):815-26. doi: 10.1016/s1097-2765(00)80391-3.

Abstract

Little is known about the mechanism of mitochondrial division. We show here that mitochondria are disrupted by mutations in a C. elegans dynamin-related protein (DRP-1). Mutant DRP-1 causes the mitochondrial matrix to retract into large blebs that are both surrounded and connected by tubules of outer membrane. This indicates that scission of the mitochondrial outer membrane is inhibited, while scission of the inner membrane still occurs. Overexpressed wild-type DRP-1 causes mitochondria to become excessively fragmented, consistent with an active role in mitochondrial scission. DRP-1 fused to GFP is observed in spots on mitochondria where scission eventually occurs. These data indicate that wild-type DRP-1 contributes to the final stages of mitochondrial division by controlling scission of the mitochondrial outer membrane.

Publication types

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

MeSH terms

  • Animals
  • Caenorhabditis elegans / cytology*
  • Caenorhabditis elegans / drug effects
  • Caenorhabditis elegans / embryology
  • Caenorhabditis elegans / genetics*
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / metabolism*
  • Cell Division
  • Cell Lineage
  • Consensus Sequence
  • Drosophila Proteins*
  • Dynamins / genetics
  • Dynamins / metabolism*
  • Female
  • Gene Expression / genetics
  • Gene Expression Profiling
  • Genes, Lethal / genetics
  • Humans
  • Intracellular Membranes / drug effects
  • Intracellular Membranes / metabolism*
  • Intracellular Membranes / ultrastructure
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mitochondria / drug effects
  • Mitochondria / metabolism*
  • Mitochondria / ultrastructure
  • Molecular Sequence Data
  • Muscles / cytology
  • Mutation / genetics
  • Neuropeptides / genetics
  • Neuropeptides / metabolism*
  • Oogenesis
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Sequence Homology, Amino Acid
  • Tetradecanoylphorbol Acetate / pharmacology
  • Vesicular Transport Proteins

Substances

  • Caenorhabditis elegans Proteins
  • Dap160 protein, Drosophila
  • Drosophila Proteins
  • Membrane Proteins
  • Neuropeptides
  • RNA, Messenger
  • Recombinant Fusion Proteins
  • Vesicular Transport Proteins
  • Dynamins
  • dynamin-related protein 1, C elegans
  • Tetradecanoylphorbol Acetate

Associated data

  • GENBANK/AF166274