The X-Linked Intellectual Disability Gene Zdhhc9 Is Essential for Dendrite Outgrowth and Inhibitory Synapse Formation

• DOI: 10.1016/j.celrep.2019.10.065
• Publication Date: 2019-11-19T15:45:46Z
• Authors: Jordan J. Shimell; Bhavin S. Shah; Stuart M. Cain; Samrat Thouta; Naila Kuhlmann; Igor Tatarnikov; D. Blair Jovellar; G. Stefano Brigidi; Jennifer Kass; Austen J. Milnerwood; Terrance P. Snutch; Shernaz X. Bamji
• Keywords: Mice, Knockout; rho GTP-Binding Proteins; 0301 basic medicine; 0303 health sciences; Epilepsy; QH301-705.5; Lipoylation; Dendrites; Hippocampus; Mice; 03 medical and health sciences; Genes, X-Linked; Intellectual Disability; Synapses; ras Proteins; Animals; Humans; Biology (General); Acyltransferases; Cells, Cultured

Palmitoylation is a reversible post-translational lipid modification that facilitates vesicular transport and subcellular localization of modified proteins. This process is catalyzed by ZDHHC enzymes that are implicated in several neurological and neurodevelopmental disorders. Loss-of-function mutations in ZDHHC9 have been identified in patients with X-linked intellectual disability (XLID) and associated with increased epilepsy risk. Loss of Zdhhc9 function in hippocampal cultures leads to shorter dendritic arbors and fewer inhibitory synapses, altering the ratio of excitatory-to-inhibitory inputs formed onto Zdhhc9-deficient cells. While Zdhhc9 promotes dendrite outgrowth through the palmitoylation of the GTPase Ras, it promotes inhibitory synapse formation through the palmitoylation of another GTPase, TC10. Zdhhc9 knockout mice exhibit seizure-like activity together with increased frequency and amplitude of both spontaneous and miniature excitatory and inhibitory postsynaptic currents. These findings present a plausible mechanism for how the loss of ZDHHC9 function may contribute to XLID and epilepsy.