Ankyrin repeat-rich membrane spanning/Kidins220 protein interacts with mammalian Septin 5

Mol Cells. 2010 Aug;30(2):143-8. doi: 10.1007/s10059-010-0099-7. Epub 2010 Jul 23.

Abstract

Neurotrophin receptors utilize specific adaptor proteins to activate signaling pathways involved in various neuronal functions, such as neurite outgrowth and cytoskeletal remodeling. The Ankyrin-Repeat Rich Membrane Spanning (ARMS)/kinase D-interacting substrate-220 kDa (Kidins220) serves as a unique downstream adaptor protein of Trk receptor tyrosine kinases. To gain insight into the role of ARMS/Kidins220, a yeast two-hybrid screen of a rat dorsal root ganglion library was performed using the C-terminal region of ARMS/Kidins220 as bait. The screen identified a mammalian septin, Septin 5 (Sept5), as an interacting protein. Co-immunoprecipitation using lysates from transiently transfected HEK-293 cells revealed the specific interaction between ARMS/Kidins220 and Sept5. Endogenous ARMS/Kidins220 and Sept5 proteins were colocalized in primary hippocampal neurons and were also predominantly expressed at the plasma membrane and in the tips of growing neurites in nerve growth factor-treated PC12 cells. Mapping of Sept5 domains important for ARMS/Kidins220 binding revealed a highly conserved N-terminal region of Sept5. The direct interaction between ARMS/Kidins220 and Sept5 suggests a possible role of ARMS/Kidins220 as a functional link between neurotrophin receptors and septins to mediate neurotrophin-induced intracellular signaling events, such as neurite outgrowth and cytoskeletal remodeling.

Publication types

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

MeSH terms

  • Actins / metabolism
  • Amino Acid Sequence
  • Animals
  • Cell Cycle Proteins / chemistry
  • Cell Cycle Proteins / metabolism*
  • Gene Deletion
  • HEK293 Cells
  • Hippocampus / cytology
  • Humans
  • Immunoprecipitation
  • Membrane Proteins / chemistry
  • Membrane Proteins / metabolism*
  • Mice
  • Molecular Sequence Data
  • Nerve Growth Factor / pharmacology
  • Neurites / drug effects
  • Neurites / metabolism
  • Neurons / drug effects
  • Neurons / metabolism
  • PC12 Cells
  • Phosphoproteins / chemistry
  • Phosphoproteins / metabolism*
  • Protein Binding / drug effects
  • Protein Interaction Mapping
  • Protein Transport / drug effects
  • Rats
  • Rats, Sprague-Dawley
  • Septins / chemistry
  • Septins / metabolism*

Substances

  • Actins
  • Cell Cycle Proteins
  • Kidins220 protein, rat
  • Membrane Proteins
  • Phosphoproteins
  • Nerve Growth Factor
  • Septin5 protein, rat
  • Septins