Mutant Huntingtin stalls ribosomes and represses protein synthesis in a cellular model of Huntington disease

The polyglutamine expansion of huntingtin (mHTT) causes Huntington disease (HD) and neurodegeneration, but the mechanisms remain unclear. Here, we found that mHtt promotes ribosome stalling and suppresses protein synthesis in mouse HD striatal neuronal cells. Depletion of mHtt enhances protein synth...

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Pubblicato in:Nat Commun
Autori principali: Eshraghi, Mehdi, Karunadharma, Pabalu P., Blin, Juliana, Shahani, Neelam, Ricci, Emiliano P., Michel, Audrey, Urban, Nicolai T., Galli, Nicole, Sharma, Manish, Ramírez-Jarquín, Uri Nimrod, Florescu, Katie, Hernandez, Jennifer, Subramaniam, Srinivasa
Natura: Artigo
Lingua:Inglês
Pubblicazione: Nature Publishing Group UK 2021
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7935949/
https://ncbi.nlm.nih.gov/pubmed/33674575
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-021-21637-y
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