Neurodegeneration in frontotemporal lobar dementia with ubiquitinated inclusions (FTLD-U), amyotrophic lateral sclerosis (ALS), and other delayed-onset diseases associated with degeneration of aging neurons involves a deficit in the degradation of the TAR DNA binding protein (TDP-43). This deficit is apparent through the characteristic pathology of a cross-section of neurodegenerative diseases, i.e., accumulation and aggregation of protein inclusions positive for TDP-43 and ubiquitin (Ub) in ALS, FTLD-U, and a large fraction of Alzheimer's Disease (AD) and Parkinson's Disease (PD) cases. Ub is a small protein conjugated singly or in polymeric chains to substrate proteins like TDP-43 that has the capacity to alter substrate fate, e.g. degradation, (in) activation, or relocation out of specific cellular compartments or protein complexes. The proposed research identifies the determinants of TDP-43 degradation, and determines the role of K63-linked polyubiquitin in rerouting of TDP-43 from degradation pathways to disease-characteristic aggregates. Half-life studies in cortical neurons and glia and in human cell lines measure the contributions of cellular alternatives for protein degradation, the proteasome and lysosome, to the degradation kinetics of endogenously expressed TDP-43. In addition, K63-linked Ub chains on TDP-43 and their association with the cell's quality control and aggregation-control machinery are identified by experiments in a cell line engineered to express modified Ub. Components of cellular quality control machinery have been shown to engage TDP-43 in neurodegenerative tissue and in models of neurodegeneration, particularly those which test the effects of insufficient proteasome or lysosome activity on substrates such as TDP-43. This insufficiency may passively develop in neurons during the course of aging or may develop due to environmental factors that affect sporadic neurodegeneration. Significant quantitative differences in interactions between TDP-43 and the Ub-dependent proteasome, lysosome, and quality control systems of cells in disease tissue will be identified. Interactions relevant to disease progression (biomarkers) or etiology (therapeutic targets) are to be confirmed by immunohistochemical staining in postmortem tissue from FTLD-U and ALS neurodegenerative disease. Finally, biochemical assays will be employed to identify specific therapeutic target(s) that deposit K63-linked Ub chains onto TDP-43;K63 Ub linkages significantly increase in neurodegenerative disease and published models of TDP-43 proteinopathy. ALS-specific mutations of TDP-43 will be tested for changes in the propensity of the protein to interact with identified interaction partners, particularly the Ub ligase that deposits K63-linked Ub chains onto TDP-43. The proposed measurements of alternative Ub chains and identification of novel disease-related proteins will rely on mass spectrometry methods and software developed by the PI and his mentors at the Emory proteomics facility and Center for Neurodegenerative Disease, where the proposed research takes place.
Frontotemporal lobar dementia (FTLD) is the leading cause of adult-onset dementia in persons under the age of 60, affecting 250,000 Americans each year and accounting for about 20 percent of pre-senile dementia cases. In FTLD and amyotrophic lateral sclerosis (ALS) subtypes, the same proteins aggregate and accumulate by unknown mechanisms, instead of being degraded within certain neurons. The proposed research examines FTLD and ALS brain tissue and models in living cells relevant to disease via proteomic, and immunochemical methods to identify mechanisms of disease progression or initiation by identifying the mechanisms that affect insufficient degradation and accumulation of the disease-associated proteins thought to be an underlying cause of FTLD-U and ALS, and potentially a cross-section of other late-onset neurodegenerative diseases including Alzheimer and Parkinson diseases. Novel disease subtypes, markers, and specific protein interactions and enzyme activities relevant as drug targets will also be discovered.
|Hales, Chadwick M; Dammer, Eric B; Diner, Ian et al. (2014) Aggregates of small nuclear ribonucleic acids (snRNAs) in Alzheimer's disease. Brain Pathol 24:344-51|
|Willmund, Felix; del Alamo, Marta; Pechmann, Sebastian et al. (2013) The cotranslational function of ribosome-associated Hsp70 in eukaryotic protein homeostasis. Cell 152:196-209|
|Dammer, Eric B; Duong, Duc M; Diner, Ian et al. (2013) Neuron enriched nuclear proteome isolated from human brain. J Proteome Res 12:3193-206|
|Bai, Bing; Hales, Chadwick M; Chen, Ping-Chung et al. (2013) U1 small nuclear ribonucleoprotein complex and RNA splicing alterations in Alzheimer's disease. Proc Natl Acad Sci U S A 110:16562-7|
|Seyfried, Nicholas T; Gozal, Yair M; Donovan, Laura E et al. (2012) Quantitative analysis of the detergent-insoluble brain proteome in frontotemporal lobar degeneration using SILAC internal standards. J Proteome Res 11:2721-38|