Huntingtin-mediated axonal transport requires arginine methylation by PRMT6-Reference-Cited by-同舟云学术

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Huntingtin-mediated axonal transport requires arginine methylation by PRMT6

Published:2021-04 Issue:2 Volume:35 Page:108980
ISSN:2211-1247
Container-title:Cell Reports
language:en
Short-container-title:Cell Reports

Author:

Migazzi Alice,Scaramuzzino Chiara^ORCID,Anderson Eric N.^ORCID,Tripathy Debasmita,Hernández Ivó H.,Grant Rogan A.^ORCID,Roccuzzo Michela^ORCID,Tosatto Laura^ORCID,Virlogeux Amandine,Zuccato Chiara,Caricasole Andrea,Ratovitski Tamara,Ross Christopher A.,Pandey Udai B.,Lucas José J.,Saudou Frédéric,Pennuto Maria^ORCID,Basso Manuela^ORCID

Funder

MIUR

University of Trento

INSERM U873

Telethon Italy

National Institutes of Health

Fondazione Italiana per la Ricerca sul Cancro Airc

Association Francaise contre les Myopathies

Agence nationale de la recherche

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference76 articles.

1. Arginine methylation is required for canonical Wnt signaling and endolysosomal trafficking;Albrecht;Proc. Natl. Acad. Sci. USA,2018

2. Traumatic injury induces stress granule formation and enhances motor dysfunctions in ALS/FTD models;Anderson;Hum. Mol. Genet.,2018

3. The non-amyloidal component region of α-synuclein is important for α-synuclein transport within axons;Anderson;Front. Cell. Neurosci.,2020

4. Post-translational modifications clustering within proteolytic domains decrease mutant huntingtin toxicity;Arbez;J. Biol. Chem.,2017

5. S-adenosylhomocysteine hydrolase deficiency in a human: a genetic disorder of methionine metabolism;Baric;Proc. Natl. Acad. Sci. USA,2004

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1. Protective Proteolysis in Huntington’s Disease: Unraveling the Role of Post-Translational Myristoylation of Huntingtin in Autophagy;Journal of Huntington's Disease;2024-09-10

2. Peripheral sequestration of huntingtin delays neuronal death and depends on N-terminal ubiquitination;Communications Biology;2024-08-18

3. Sequencing-guided design of genetically encoded small RNAs targeting CAG repeats for selective inhibition of mutant huntingtin;Molecular Therapy - Nucleic Acids;2024-06

4. Neuropathogenesis-on-chips for neurodegenerative diseases;Nature Communications;2024-03-12

5. Spliceosome-mediated RNA <i>trans</i>-splicing: a strategy for Huntington’s disease gene therapy;BIOCELL;2024

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