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

Huntington disease (HD) is a neurodegenerative disorder caused by the expansion of a polyglutamine tract in the huntingtin (mHtt) protein. Here the authors suggest that mHtt promotes ribosome stalling and inhibits protein synthesis.

Guardado en:
Detalles Bibliográficos
Autores principales: Mehdi Eshraghi, Pabalu P. Karunadharma, Juliana Blin, Neelam Shahani, Emiliano P. Ricci, Audrey Michel, Nicolai T. Urban, Nicole Galli, Manish Sharma, Uri Nimrod Ramírez-Jarquín, Katie Florescu, Jennifer Hernandez, Srinivasa Subramaniam
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
Materias:
Q
Acceso en línea:https://doaj.org/article/a00d7181daf04071b4b42dae11f057fa
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:a00d7181daf04071b4b42dae11f057fa
record_format dspace
spelling oai:doaj.org-article:a00d7181daf04071b4b42dae11f057fa2021-12-02T13:33:01ZMutant Huntingtin stalls ribosomes and represses protein synthesis in a cellular model of Huntington disease10.1038/s41467-021-21637-y2041-1723https://doaj.org/article/a00d7181daf04071b4b42dae11f057fa2021-03-01T00:00:00Zhttps://doi.org/10.1038/s41467-021-21637-yhttps://doaj.org/toc/2041-1723Huntington disease (HD) is a neurodegenerative disorder caused by the expansion of a polyglutamine tract in the huntingtin (mHtt) protein. Here the authors suggest that mHtt promotes ribosome stalling and inhibits protein synthesis.Mehdi EshraghiPabalu P. KarunadharmaJuliana BlinNeelam ShahaniEmiliano P. RicciAudrey MichelNicolai T. UrbanNicole GalliManish SharmaUri Nimrod Ramírez-JarquínKatie FlorescuJennifer HernandezSrinivasa SubramaniamNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-20 (2021)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Mehdi Eshraghi
Pabalu P. Karunadharma
Juliana Blin
Neelam Shahani
Emiliano P. Ricci
Audrey Michel
Nicolai T. Urban
Nicole Galli
Manish Sharma
Uri Nimrod Ramírez-Jarquín
Katie Florescu
Jennifer Hernandez
Srinivasa Subramaniam
Mutant Huntingtin stalls ribosomes and represses protein synthesis in a cellular model of Huntington disease
description Huntington disease (HD) is a neurodegenerative disorder caused by the expansion of a polyglutamine tract in the huntingtin (mHtt) protein. Here the authors suggest that mHtt promotes ribosome stalling and inhibits protein synthesis.
format article
author Mehdi Eshraghi
Pabalu P. Karunadharma
Juliana Blin
Neelam Shahani
Emiliano P. Ricci
Audrey Michel
Nicolai T. Urban
Nicole Galli
Manish Sharma
Uri Nimrod Ramírez-Jarquín
Katie Florescu
Jennifer Hernandez
Srinivasa Subramaniam
author_facet Mehdi Eshraghi
Pabalu P. Karunadharma
Juliana Blin
Neelam Shahani
Emiliano P. Ricci
Audrey Michel
Nicolai T. Urban
Nicole Galli
Manish Sharma
Uri Nimrod Ramírez-Jarquín
Katie Florescu
Jennifer Hernandez
Srinivasa Subramaniam
author_sort Mehdi Eshraghi
title Mutant Huntingtin stalls ribosomes and represses protein synthesis in a cellular model of Huntington disease
title_short Mutant Huntingtin stalls ribosomes and represses protein synthesis in a cellular model of Huntington disease
title_full Mutant Huntingtin stalls ribosomes and represses protein synthesis in a cellular model of Huntington disease
title_fullStr Mutant Huntingtin stalls ribosomes and represses protein synthesis in a cellular model of Huntington disease
title_full_unstemmed Mutant Huntingtin stalls ribosomes and represses protein synthesis in a cellular model of Huntington disease
title_sort mutant huntingtin stalls ribosomes and represses protein synthesis in a cellular model of huntington disease
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/a00d7181daf04071b4b42dae11f057fa
work_keys_str_mv AT mehdieshraghi mutanthuntingtinstallsribosomesandrepressesproteinsynthesisinacellularmodelofhuntingtondisease
AT pabalupkarunadharma mutanthuntingtinstallsribosomesandrepressesproteinsynthesisinacellularmodelofhuntingtondisease
AT julianablin mutanthuntingtinstallsribosomesandrepressesproteinsynthesisinacellularmodelofhuntingtondisease
AT neelamshahani mutanthuntingtinstallsribosomesandrepressesproteinsynthesisinacellularmodelofhuntingtondisease
AT emilianopricci mutanthuntingtinstallsribosomesandrepressesproteinsynthesisinacellularmodelofhuntingtondisease
AT audreymichel mutanthuntingtinstallsribosomesandrepressesproteinsynthesisinacellularmodelofhuntingtondisease
AT nicolaiturban mutanthuntingtinstallsribosomesandrepressesproteinsynthesisinacellularmodelofhuntingtondisease
AT nicolegalli mutanthuntingtinstallsribosomesandrepressesproteinsynthesisinacellularmodelofhuntingtondisease
AT manishsharma mutanthuntingtinstallsribosomesandrepressesproteinsynthesisinacellularmodelofhuntingtondisease
AT urinimrodramirezjarquin mutanthuntingtinstallsribosomesandrepressesproteinsynthesisinacellularmodelofhuntingtondisease
AT katieflorescu mutanthuntingtinstallsribosomesandrepressesproteinsynthesisinacellularmodelofhuntingtondisease
AT jenniferhernandez mutanthuntingtinstallsribosomesandrepressesproteinsynthesisinacellularmodelofhuntingtondisease
AT srinivasasubramaniam mutanthuntingtinstallsribosomesandrepressesproteinsynthesisinacellularmodelofhuntingtondisease
_version_ 1718392870969278464