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Title[redir]:
Palmitoylation of huntingtin by HIP14is essential for its trafficking and function | Nature Neuroscience
Description:
Post-translational modification by the lipid palmitate is crucial for the correct targeting and function of many proteins. Here we show that huntingtin (htt) is normally palmitoylated at cysteine 214, which is essential for its trafficking and function. The palmitoylation and distribution of htt are regulated by the palmitoyl transferase huntingtin interacting protein 14 (HIP14). Expansion of the polyglutamine tract of htt, which causes Huntington disease, results in reduced interaction between mutant htt and HIP14 and consequently in a marked reduction in palmitoylation. Mutation of the palmitoylation site of htt, making it palmitoylation resistant, accelerates inclusion formation and increases neuronal toxicity. Downregulation of HIP14 in mouse neurons expressing wild-type and mutant htt increases inclusion formation, whereas overexpression of HIP14 substantially reduces inclusions. These results suggest that the expansion of the polyglutamine tract in htt results in decreased palmitoylation, which contributes to the formation of inclusion bodies and enhanced neuronal toxicity.
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Keywords {π}
article, pubmed, cas, google, scholar, huntingtin, nature, palmitoylation, htt, disease, protein, research, hip, access, biol, cell, function, trafficking, neuronal, huntingtons, mutant, central, content, data, elhusseini, toxicity, mol, performed, cookies, huang, michael, hayden, polyglutamine, huntington, inclusion, hum, genet, supported, canada, british, columbia, privacy, mouse, neurons, pdf, open, model, neurosci, chem, mrh,
Topics {βοΈ}
n-methyl-d-aspartate receptor-mediated excitotoxicity nature portfolio permissions reprints privacy policy advertising neuronal development nature 431 nature social media palmitoylation-mediated synaptic regulation specific ubiquitin-conjugating enzyme research infrastructure unit alaa el-husseini canada research chair family research institute full-length mutant htt btn-bmcc palmitoylation assays springerlink instant access polyglutamine expansion-specific interaction lysosomal palmitoyl-protein thioesterase permissions huntingtin-interacting protein hip14 full-length htt palmitoylation rat brain neurons el-husseini health research medical research pharmacal research htt-transfected cos cells mutant huntingtin fragments increases neuronal toxicity synaptic strength regulated privacy [3h]palmitoylation assays personal data yac128 mouse model competing financial interests palmitoyl-protein thioesterase 2 palmitoyl-protein thioesterase full-length htt article yanai ampa receptor trafficking enhanced neuronal toxicity accelerates inclusion formation palmitoyl transferase involved wellcome/mrc building explore content subscription content function anat yanai characterized hip14 sirna
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headline:Palmitoylation of huntingtin by HIP14is essential for its trafficking and function
description:Post-translational modification by the lipid palmitate is crucial for the correct targeting and function of many proteins. Here we show that huntingtin (htt) is normally palmitoylated at cysteine 214, which is essential for its trafficking and function. The palmitoylation and distribution of htt are regulated by the palmitoyl transferase huntingtin interacting protein 14 (HIP14). Expansion of the polyglutamine tract of htt, which causes Huntington disease, results in reduced interaction between mutant htt and HIP14 and consequently in a marked reduction in palmitoylation. Mutation of the palmitoylation site of htt, making it palmitoylation resistant, accelerates inclusion formation and increases neuronal toxicity. Downregulation of HIP14 in mouse neurons expressing wild-type and mutant htt increases inclusion formation, whereas overexpression of HIP14 substantially reduces inclusions. These results suggest that the expansion of the polyglutamine tract in htt results in decreased palmitoylation, which contributes to the formation of inclusion bodies and enhanced neuronal toxicity.
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headline:Palmitoylation of huntingtin by HIP14is essential for its trafficking and function
description:Post-translational modification by the lipid palmitate is crucial for the correct targeting and function of many proteins. Here we show that huntingtin (htt) is normally palmitoylated at cysteine 214, which is essential for its trafficking and function. The palmitoylation and distribution of htt are regulated by the palmitoyl transferase huntingtin interacting protein 14 (HIP14). Expansion of the polyglutamine tract of htt, which causes Huntington disease, results in reduced interaction between mutant htt and HIP14 and consequently in a marked reduction in palmitoylation. Mutation of the palmitoylation site of htt, making it palmitoylation resistant, accelerates inclusion formation and increases neuronal toxicity. Downregulation of HIP14 in mouse neurons expressing wild-type and mutant htt increases inclusion formation, whereas overexpression of HIP14 substantially reduces inclusions. These results suggest that the expansion of the polyglutamine tract in htt results in decreased palmitoylation, which contributes to the formation of inclusion bodies and enhanced neuronal toxicity.
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