A Mouse Model of X-linked Intellectual Disability Associated with Impaired Removal of Histone Methylation

Cell Rep. 2016 Feb 9;14(5):1000-1009. doi: 10.1016/j.celrep.2015.12.091. Epub 2016 Jan 21.

Abstract

Mutations in a number of chromatin modifiers are associated with human neurological disorders. KDM5C, a histone H3 lysine 4 di- and tri-methyl (H3K4me2/3)-specific demethylase, is frequently mutated in X-linked intellectual disability (XLID) patients. Here, we report that disruption of the mouse Kdm5c gene recapitulates adaptive and cognitive abnormalities observed in XLID, including impaired social behavior, memory deficits, and aggression. Kdm5c-knockout brains exhibit abnormal dendritic arborization, spine anomalies, and altered transcriptomes. In neurons, Kdm5c is recruited to promoters that harbor CpG islands decorated with high levels of H3K4me3, where it fine-tunes H3K4me3 levels. Kdm5c predominantly represses these genes, which include members of key pathways that regulate the development and function of neuronal circuitries. In summary, our mouse behavioral data strongly suggest that KDM5C mutations are causal to XLID. Furthermore, our findings suggest that loss of KDM5C function may impact gene expression in multiple regulatory pathways relevant to the clinical phenotypes.

Publication types

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

MeSH terms

  • Aggression
  • Animals
  • Brain / pathology
  • CpG Islands
  • Dendritic Spines / pathology
  • Disease Models, Animal
  • Gene Expression Regulation
  • Genes, X-Linked*
  • Histone Demethylases
  • Histones / metabolism*
  • Intellectual Disability / genetics*
  • Lysine / metabolism
  • Memory
  • Methylation
  • Mice, Knockout
  • Oxidoreductases, N-Demethylating / deficiency
  • Oxidoreductases, N-Demethylating / metabolism
  • Promoter Regions, Genetic
  • Social Behavior
  • Transcription, Genetic

Substances

  • Histones
  • Histone Demethylases
  • Kdm5c protein, mouse
  • Oxidoreductases, N-Demethylating
  • Lysine