CYFIP2 p.Arg87Cys Causes Neurological Defects and Degradation of CYFIP2

Ann Neurol. 2023 Jan;93(1):155-163. doi: 10.1002/ana.26535. Epub 2022 Oct 26.

Abstract

Here, we report the generation and comprehensive characterization of a knockin mouse model for the hotspot p.Arg87Cys variant of the cytoplasmic FMR1-interacting protein 2 (CYFIP2) gene, which was recently identified in individuals diagnosed with West syndrome, a developmental and epileptic encephalopathy. The Cyfip2+/R87C mice recapitulated many neurological and neurobehavioral phenotypes of the patients, including spasmlike movements, microcephaly, and impaired social communication. Age-progressive cytoarchitectural disorganization and gliosis were also identified in the hippocampus of Cyfip2+/R87C mice. Beyond identifying a decrease in CYFIP2 protein levels in the Cyfip2+/R87C brains, we demonstrated that the p.Arg87Cys variant enhances ubiquitination and proteasomal degradation of CYFIP2. ANN NEUROL 2023;93:155-163.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing* / genetics
  • Animals
  • Brain / metabolism
  • Fragile X Mental Retardation Protein
  • Hippocampus / metabolism
  • Mice
  • Spasms, Infantile* / genetics

Substances

  • Adaptor Proteins, Signal Transducing
  • Fmr1 protein, mouse
  • Fragile X Mental Retardation Protein
  • Cyfip2 protein, mouse