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Altered palmitoylation and neuropathological deficits in mice lacking HIP14
Authors:Singaraja Roshni R  Huang Kun  Sanders Shaun S  Milnerwood Austen J  Hines Rochelle  Lerch Jason P  Franciosi Sonia  Drisdel Renaldo C  Vaid Kuljeet  Young Fiona B  Doty Crystal  Wan Junmei  Bissada Nagat  Henkelman R Mark  Green William N  Davis Nicholas G  Raymond Lynn A  Hayden Michael R
Institution:Centre for Molecular Medicine and Therapeutics and Child and Family Research Institute, Vancouver, BC, Canada.
Abstract:Huntingtin interacting protein 14 (HIP14, ZDHHC17) is a huntingtin (HTT) interacting protein with palmitoyl transferase activity. In order to interrogate the function of Hip14, we generated mice with disruption in their Hip14 gene. Hip14-/- mice displayed behavioral, biochemical and neuropathological defects that are reminiscent of Huntington disease (HD). Palmitoylation of other HIP14 substrates, but not Htt, was reduced in the Hip14-/- mice. Hip14 is dysfunctional in the presence of mutant htt in the YAC128 mouse model of HD, suggesting that altered palmitoylation mediated by HIP14 may contribute to HD.
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