Roles of the multivalent dynein adaptors BicD2 and RILP in neurons

Neurosci Lett. 2021 May 1:752:135796. doi: 10.1016/j.neulet.2021.135796. Epub 2021 Mar 2.

Abstract

Cytoplasmic dynein is responsible for all forms of retrograde transport in neurons and other cells. Work over several years has led to the identification of a class of coiled-coil domain containing "adaptor" proteins that are responsible for expanding dynein's range of cargo interactions, as well as regulating dynein motor behavior. This brief review focuses first on the BicD family of adaptor proteins, which clearly serve to expand the number of dynein cargo interactions. RILP, another adaptor protein, also interacts with multiple proteins. Surprisingly, this is to mediate a series of steps within a common pathway, higher eukaryotic autophagy. These distinct features have important implications for understanding the full range of dynein adaptor functions.

Keywords: Adaptor proteins; Autophagy; BicD2; Brain development; Dynein; RILP.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism*
  • Animals
  • Autophagy*
  • Humans
  • Microfilament Proteins / metabolism
  • Microtubule-Associated Proteins / metabolism*
  • Molecular Chaperones / metabolism
  • Nerve Tissue Proteins / metabolism
  • Neurons / metabolism*
  • Nuclear Pore Complex Proteins / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • BICD2 protein, human
  • Microfilament Proteins
  • Microtubule-Associated Proteins
  • Molecular Chaperones
  • Nerve Tissue Proteins
  • Nuclear Pore Complex Proteins
  • RILP protein, human
  • SYNE2 protein, human
  • ran-binding protein 2