Literature DB >> 18637946

Huntington's disease: degradation of mutant huntingtin by autophagy.

Sovan Sarkar1, David C Rubinsztein.   

Abstract

Autophagy is a nonspecific bulk degradation pathway for long-lived cytoplasmic proteins, protein complexes, or damaged organelles. This process is also a major degradation pathway for many aggregate-prone, disease-causing proteins associated with neurodegenerative disorders, such as mutant huntingtin in Huntington's disease. In this review, we discuss factors regulating the degradation of mutant huntingtin by autophagy. We also report the growing list of new drugs/pathways that upregulate autophagy to enhance the clearance of this mutant protein, as autophagy upregulation may be a tractable strategy for the treatment of Huntington's disease.

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Year:  2008        PMID: 18637946     DOI: 10.1111/j.1742-4658.2008.06562.x

Source DB:  PubMed          Journal:  FEBS J        ISSN: 1742-464X            Impact factor:   5.542


  90 in total

Review 1.  Engineered antibody therapies to counteract mutant huntingtin and related toxic intracellular proteins.

Authors:  David C Butler; Julie A McLear; Anne Messer
Journal:  Prog Neurobiol       Date:  2011-11-18       Impact factor: 11.685

2.  Early autophagic response in a novel knock-in model of Huntington disease.

Authors:  Mary Y Heng; Duy K Duong; Roger L Albin; Sara J Tallaksen-Greene; Jesse M Hunter; Mathieu J Lesort; Alex Osmand; Henry L Paulson; Peter J Detloff
Journal:  Hum Mol Genet       Date:  2010-07-08       Impact factor: 6.150

3.  The vacuole import and degradation pathway utilizes early steps of endocytosis and actin polymerization to deliver cargo proteins to the vacuole for degradation.

Authors:  C Randell Brown; Danielle Dunton; Hui-Ling Chiang
Journal:  J Biol Chem       Date:  2009-11-05       Impact factor: 5.157

4.  Identification of a post-translationally myristoylated autophagy-inducing domain released by caspase cleavage of huntingtin.

Authors:  Dale D O Martin; Ryan J Heit; Megan C Yap; Michael W Davidson; Michael R Hayden; Luc G Berthiaume
Journal:  Hum Mol Genet       Date:  2014-01-23       Impact factor: 6.150

5.  Rhes, a striatal-selective protein implicated in Huntington disease, binds beclin-1 and activates autophagy.

Authors:  Robert G Mealer; Alexandra J Murray; Neelam Shahani; Srinivasa Subramaniam; Solomon H Snyder
Journal:  J Biol Chem       Date:  2013-12-09       Impact factor: 5.157

6.  mTOR regulates tau phosphorylation and degradation: implications for Alzheimer's disease and other tauopathies.

Authors:  Antonella Caccamo; Andrea Magrì; David X Medina; Elena V Wisely; Manuel F López-Aranda; Alcino J Silva; Salvatore Oddo
Journal:  Aging Cell       Date:  2013-03-24       Impact factor: 9.304

Review 7.  Mitochondrial quality control and neurological disease: an emerging connection.

Authors:  Inês Pimenta de Castro; L Miguel Martins; Roberta Tufi
Journal:  Expert Rev Mol Med       Date:  2010-04-19       Impact factor: 5.600

8.  Deletion of the huntingtin polyglutamine stretch enhances neuronal autophagy and longevity in mice.

Authors:  Shuqiu Zheng; Erin B D Clabough; Sovan Sarkar; Marie Futter; David C Rubinsztein; Scott O Zeitlin
Journal:  PLoS Genet       Date:  2010-02-05       Impact factor: 5.917

9.  Cargo recognition failure is responsible for inefficient autophagy in Huntington's disease.

Authors:  Marta Martinez-Vicente; Zsolt Talloczy; Esther Wong; Guomei Tang; Hiroshi Koga; Susmita Kaushik; Rosa de Vries; Esperanza Arias; Spike Harris; David Sulzer; Ana Maria Cuervo
Journal:  Nat Neurosci       Date:  2010-04-11       Impact factor: 24.884

10.  Laforin, the most common protein mutated in Lafora disease, regulates autophagy.

Authors:  Carmen Aguado; Sovan Sarkar; Viktor I Korolchuk; Olga Criado; Santiago Vernia; Patricia Boya; Pascual Sanz; Santiago Rodríguez de Córdoba; Erwin Knecht; David C Rubinsztein
Journal:  Hum Mol Genet       Date:  2010-05-07       Impact factor: 6.150

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