Literature DB >> 30452420

Longitudinal Biochemical Assay Analysis of Mutant Huntingtin Exon 1 Protein in R6/2 Mice.

Eva L Morozko1, Joseph Ochaba1,2, Sarah J Hernandez1, Alice Lau2, Isabella Sanchez1, Iliana Orellana3, Lexi Kopan1, Joshua Crapser1, Janet H Duong1, Julia Overman1, Silvia Yeung3, Joan S Steffan2,3, Jack Reidling3, Leslie M Thompson1,2,3.   

Abstract

BACKGROUND: Biochemical analysis of mutant huntingtin (mHTT) aggregation species in HD mice is a common measure to track disease. A longitudinal and systematic study of how tissue processing affects detection of conformers has not yet been reported. Understanding the homeostatic flux of mHTT over time and under different processing conditions would aid in interpretation of pre-clinical assessments of disease interventions.
OBJECTIVE: Provide a systematic evaluation of tissue lysis methods and molecular and biochemical assays in parallel with behavioral readouts in R6/2 mice to establish a baseline for HTT exon1 protein accumulation.
METHODS: Established biochemical methods were used to process tissue from R6/2 mice of specific ages following behavior tasks. Aggregation states and accumulation of mHTT exon 1 protein were evaluated using multiple break and assay methods to determine potential conformational flux assay specificity in detection of mHTT species, and tissue specificity of conformers.
RESULTS: Detection of mHTT exon 1 protein species varied based on biochemical processing and analysis providing a baseline for subsequent studies in R6/2 mice. Insoluble, high molecular weight species of mHTT exon 1 protein increased and tracked with onset of behavioral impairments in R6/2 mice using multiple assay methods.
CONCLUSIONS: Conformational flux from soluble monomer to high molecular weight, insoluble species of mHTT exon 1 protein was generally consistent for multiple assay methods throughout R6/2 disease progression; however, the results support the use of multiple biochemical techniques to detect mHTT exon 1 protein species for preclinical assessments in HD mouse models expressing mHTT exon 1 protein.

Entities:  

Keywords:  Huntingtin; Huntington’s disease; aggregation; conformer; protein aggregates; protein homeostasis

Mesh:

Substances:

Year:  2018        PMID: 30452420      PMCID: PMC6294605          DOI: 10.3233/JHD-180329

Source DB:  PubMed          Journal:  J Huntingtons Dis        ISSN: 1879-6397


  42 in total

1.  Nuclear and neuropil aggregates in Huntington's disease: relationship to neuropathology.

Authors:  C A Gutekunst; S H Li; H Yi; J S Mulroy; S Kuemmerle; R Jones; D Rye; R J Ferrante; S M Hersch; X J Li
Journal:  J Neurosci       Date:  1999-04-01       Impact factor: 6.167

2.  New anti-huntingtin monoclonal antibodies: implications for huntingtin conformation and its binding proteins.

Authors:  J Ko; S Ou; P H Patterson
Journal:  Brain Res Bull       Date:  2001 Oct-Nov 1       Impact factor: 4.077

Review 3.  Mechanisms underlying neurodegeneration in Huntington disease: applications to novel disease-modifying therapies.

Authors:  Christopher A Ross; Martin Kronenbuerger; Wenzhen Duan; Russell L Margolis
Journal:  Handb Clin Neurol       Date:  2017

4.  Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice.

Authors:  L Mangiarini; K Sathasivam; M Seller; B Cozens; A Harper; C Hetherington; M Lawton; Y Trottier; H Lehrach; S W Davies; G P Bates
Journal:  Cell       Date:  1996-11-01       Impact factor: 41.582

5.  Potential function for the Huntingtin protein as a scaffold for selective autophagy.

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Journal:  Proc Natl Acad Sci U S A       Date:  2014-11-10       Impact factor: 11.205

6.  Mutant huntingtin fragments form oligomers in a polyglutamine length-dependent manner in vitro and in vivo.

Authors:  Justin Legleiter; Emily Mitchell; Gregor P Lotz; Ellen Sapp; Cheping Ng; Marian DiFiglia; Leslie M Thompson; Paul J Muchowski
Journal:  J Biol Chem       Date:  2010-03-10       Impact factor: 5.157

7.  Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation.

Authors:  S W Davies; M Turmaine; B A Cozens; M DiFiglia; A H Sharp; C A Ross; E Scherzinger; E E Wanker; L Mangiarini; G P Bates
Journal:  Cell       Date:  1997-08-08       Impact factor: 41.582

8.  Sensitive biochemical aggregate detection reveals aggregation onset before symptom development in cellular and murine models of Huntington's disease.

Authors:  Andreas Weiss; Corinna Klein; Ben Woodman; Kirupa Sathasivam; Miriam Bibel; Etienne Régulier; Gillian P Bates; Paolo Paganetti
Journal:  J Neurochem       Date:  2007-11-06       Impact factor: 5.372

9.  Identifying polyglutamine protein species in situ that best predict neurodegeneration.

Authors:  Jason Miller; Montserrat Arrasate; Elizabeth Brooks; Clare Peters Libeu; Justin Legleiter; Danny Hatters; Jessica Curtis; Kenneth Cheung; Preethi Krishnan; Siddhartha Mitra; Kartika Widjaja; Benjamin A Shaby; Gregor P Lotz; Yvonne Newhouse; Emily J Mitchell; Alex Osmand; Michelle Gray; Vanitha Thulasiramin; Frédéric Saudou; Mark Segal; X William Yang; Eliezer Masliah; Leslie M Thompson; Paul J Muchowski; Karl H Weisgraber; Steven Finkbeiner
Journal:  Nat Chem Biol       Date:  2011-10-30       Impact factor: 15.040

10.  SUMO-2 and PIAS1 modulate insoluble mutant huntingtin protein accumulation.

Authors:  Jacqueline Gire O'Rourke; Jaclyn R Gareau; Joseph Ochaba; Wan Song; Tamás Raskó; David Reverter; John Lee; Alex Mas Monteys; Judit Pallos; Lisa Mee; Malini Vashishtha; Barbara L Apostol; Thomas Peter Nicholson; Katalin Illes; Ya-Zhen Zhu; Mary Dasso; Gillian P Bates; Marian Difiglia; Beverly Davidson; Erich E Wanker; J Lawrence Marsh; Christopher D Lima; Joan S Steffan; Leslie M Thompson
Journal:  Cell Rep       Date:  2013-07-18       Impact factor: 9.423

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  2 in total

1.  Microglial depletion prevents extracellular matrix changes and striatal volume reduction in a model of Huntington's disease.

Authors:  Joshua D Crapser; Joseph Ochaba; Neelakshi Soni; Jack C Reidling; Leslie M Thompson; Kim N Green
Journal:  Brain       Date:  2020-01-01       Impact factor: 13.501

2.  IKKβ slows Huntington's disease progression in R6/1 mice.

Authors:  Joseph Ochaba; Gianna Fote; Marketta Kachemov; Soe Thein; Sylvia Y Yeung; Alice L Lau; Sarah Hernandez; Ryan G Lim; Malcolm Casale; Michael J Neel; Edwin S Monuki; Jack Reidling; David E Housman; Leslie M Thompson; Joan S Steffan
Journal:  Proc Natl Acad Sci U S A       Date:  2019-05-14       Impact factor: 11.205

  2 in total

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