Fragile X mental retardation protein controls gating of the sodium-activated potassium channel Slack

Nat Neurosci. 2010 Jul;13(7):819-21. doi: 10.1038/nn.2563. Epub 2010 May 30.

Abstract

In humans, the absence of Fragile X mental retardation protein (FMRP), an RNA-binding protein, results in Fragile X syndrome, the most common inherited form of intellectual disability. Using biochemical and electrophysiological studies, we found that FMRP binds to the C terminus of the Slack sodium-activated potassium channel to activate the channel in mice. Our findings suggest that Slack activity provides a link between patterns of neuronal firing and changes in protein translation.

Publication types

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

MeSH terms

  • Animals
  • Disease Models, Animal
  • Fragile X Mental Retardation Protein / physiology*
  • Ion Channel Gating / physiology*
  • Mice
  • Nerve Tissue Proteins
  • Potassium Channels / metabolism*
  • Potassium Channels, Sodium-Activated

Substances

  • Nerve Tissue Proteins
  • Potassium Channels
  • Potassium Channels, Sodium-Activated
  • Slo2 protein, mouse
  • Fragile X Mental Retardation Protein