- Title Information
- Title
- The role of plastin in motor neuron diseases and identifying genetic modifiers of spinal muscular atrophy
- Name:
Personal
- Name Part
- Walsh, Melissa Brietta
- Role
- Role Term:
Text
- creator
- Origin Information
- Copyright Date
- 2015
- Physical Description
- Extent
- 13, 181 p.
- digitalOrigin
- born digital
- Note
- Thesis (Ph.D. -- Brown University (2015)
- Name:
Personal
- Name Part
- Hart, Anne
- Role
- Role Term:
Text
- Director
- Name:
Personal
- Name Part
- Sahin, Mustafa
- Role
- Role Term:
Text
- Reader
- Name:
Personal
- Name Part
- Reenan, Robert
- Role
- Role Term:
Text
- Reader
- Name:
Personal
- Name Part
- Mowry, Kimberly
- Role
- Role Term:
Text
- Reader
- Name:
Personal
- Name Part
- Morrow, Eric
- Role
- Role Term:
Text
- Reader
- Name:
Corporate
- Name Part
- Brown University. BIOMED: Molecular Biology, Cell Biology, and Biochemistry
- Role
- Role Term:
Text
- sponsor
- Genre (aat)
- theses
- Abstract
- Abstract of The role of plastin in motor neuron disease and identifying genetic modifiers of spinal muscular atrophy, by Melissa B. Walsh, Ph. D., Brown University, May 2015.
Neurodegenerative diseases are becoming increasingly prevalent. This growth in incidence correlates with a high demand for treatment, which is not readily available for most of these diseases. Identification of common genetic modifiers that affect multiple diseases would enable a better understanding of the mechanism of pathogenesis of these diseases and provide possible therapeutic targets. Using the model system Caenorhabditis elegans (C. elegans) we assessed whether plastin, a previously identified genetic modifier in patients of Spinal Muscular Atrophy (SMA), was able to ameliorate the behavioral defects found in nematode models of SMA, Amyotrophic Lateral Sclerosis (ALS) and polyglutamine toxicity disease. Further genetic and biochemical screening was done in order to understand how plastin acts to ameliorate SMA defects. This study showed that plastin, an actin bundling protein is able to suppress various behavioral defects across the three disease models tested. It also identified the ortholog to heterogeneous nuclear ribonucleoprotein F and H (hnRNP F and hnRNP H) as a genetic modifier in C. elegans models of SMA and ALS. Analysis using a vertebrate neuronal system showed that SMN co-immunoprecipitates with PLS3, hnRNP F and hnRNP H. Staining in mouse primary motor neurons also shows a co-localization of SMN with PLS3, hnRNP F and hnRNP H in motor neuron processes. The genetic data in C. elegans combined with the vertebrate protein data suggest that SMN, PLS3 and hnRNP F/H could act in a complex together in motor neuron processes that is pertinent to SMA pathogenesis. Taken together, the identification of plastin and hnRNP F/H as cross disease modifiers suggests that they could be targeting a common mechanism perturbed in both diseases. Further validation in vertebrate disease models is required and if true would provide a novel therapeutic target for these diseases.
- Subject
- Topic
- C. elegans
- Subject
- Topic
- plastin
- Subject
- Topic
- ALS
- Subject
- Topic
- SMA
- Subject
- Topic
- motor neuron disease
- Subject (FAST)
(authorityURI="http://id.worldcat.org/fast", valueURI="http://id.worldcat.org/fast/843844")
- Topic
- Caenorhabditis elegans
- Subject (FAST)
(authorityURI="http://id.worldcat.org/fast", valueURI="http://id.worldcat.org/fast/1129903")
- Topic
- Spinal muscular atrophy
- Subject (FAST)
(authorityURI="http://id.worldcat.org/fast", valueURI="http://id.worldcat.org/fast/1027640")
- Topic
- Motor neurons--Diseases
- Record Information
- Record Content Source (marcorg)
- RPB
- Record Creation Date
(encoding="iso8601")
- 20150601
- Language
- Language Term:
Code (ISO639-2B)
- eng
- Language Term:
Text
- English
- Identifier:
DOI
- 10.7301/Z0GB22F8
- Access Condition:
rights statement
(href="http://rightsstatements.org/vocab/InC/1.0/")
- In Copyright
- Access Condition:
restriction on access
- Collection is open for research.
- Type of Resource (primo)
- dissertations