Project Grant R21NS139090

THE MECHANISM AND ROLE OF ANDROGEN RECEPTOR SERINE 16 PHOSPHORYLATION IN SBMA - MANY NEURODEGENERATIVE DISEASES, INCLUDING ALZHEIMER'S DISEASE, PARKINSON'S DISEASE AND THE POLYGLUTAMINE DISEASES, RESULT FROM PROTEIN MISFOLDING AND ACCUMULATION DUE TO A VARIETY OF GENETIC AND/OR ENVIRONMENTAL CAUSES. SPINAL AND BULBAR MUSCULAR ATROPHY (SBMA) IS AN ADULT-ONSET, INHERITED NEUROMUSCULAR DISEASE THAT IS CAUSED BY POLYGLUTAMINE EXPANSION WITHIN THE ANDROGEN RECEPTOR (AR); IT IS RELATED TO OTHER NEURODEGENERATIVE DISEASES CAUSED BY POLYGLUTAMINE EXPANSION, INCLUDING HUNTINGTON'S DISEASE AND SEVERAL SPINOCEREBELLAR ATAXIAS. ALTHOUGH THE PRECISE PATHWAY LEADING TO NEURONAL DYSFUNCTION AND DEATH IS UNKNOWN, THE EVALUATION OF TRANSGENIC MOUSE AND CELL MODELS OF THESE DISEASES HAS YIELDED MECHANISTIC INSIGHTS TO DISEASE PATHOGENESIS. SBMA STANDS APART FROM OTHER POLYGLUTAMINE DISEASES IN THAT ITS ONSET AND PROGRESSION ARE DEPENDENT ON AR ANDROGENIC LIGANDS. MANY CELL AND MOUSE MODELS OF SBMA REPRODUCE THE ANDROGEN- AND POLYGLUTAMINE-DEPENDENT NUCLEAR AR AGGREGATION SEEN IN PATIENTS, AS WELL AS ITS CONSEQUENT TOXICITY, MAKING THESE MODELS HIGHLY USEFUL FOR THE ANALYSIS OF THE MECHANISTIC BASIS FOR UPSTREAM EVENTS INVOLVED IN AR TOXICITY. OUR LONG- TERM OBJECTIVES ARE TO USE THESE MODELS TO DEVELOP A MECHANISTIC UNDERSTANDING OF STEPS IN SBMA PATHOGENESIS THAT OCCUR IN RESPONSE TO HORMONE BINDING AND TO DEVELOP THERAPEUTIC APPROACHES BASED ON THAT UNDERSTANDING. SUCH STUDIES PREVIOUSLY REVEALED THAT A SPECIFIC CONFORMATIONAL STATE, THE INTERACTION BETWEEN THE AMINO (N)- AND CARBOXYL (C)- TERMINAL ENDS OF THE AR THAT OCCURS UPON HORMONE BINDING (N/C INTERACTION), IS REQUIRED FOR ITS AGGREGATION AND TOXICITY; INHIBITION OF THE N/C INTERACTION BY GENETIC OR PHARMACOLOGIC MEANS IS PROTECTIVE BOTH IN VITRO AND IN VIVO. MOREOVER, WE FOUND THAT NOT ONLY IS SER-16 HYPERPHOSPHORYLATED UPON PREVENTING THE AR N/C INTERACTION BUT THIS PHOSPHORYLATION IS REQUIRED FOR PROTECTION, AS MUTATION OF SER-16 TO THE UN-PHOSPHORYLATABLE AMINO ACID ALANINE ABROGATED THE NEUROPROTECTION. WE PROPOSE IN THIS APPLICATION TO FURTHER UNDERSTAND THE MECHANISM UNDERLYING THE ROLE OF SER-16 PHOSPHORYLATION IN DISEASE BY IDENTIFYING THE KINASE RESPONSIBLE FOR SER-16 PHOSPHORYLATION (AIM 1) AND USING THIS INFORMATION TO EXPLORE THE IMPACT OF SER-16 PHOSPHORYLATION ON AR METABOLISM AND SBMA-RELATED CELLULAR AND BIOCHEMICAL PHENOTYPES (AIM 2). WE ANTICIPATE THAT RESULTS FROM THESE STUDIES WILL LEAD US TO A NEW UNDERSTANDING OF THE MOLECULAR PATHOGENESIS OF SBMA AND ENHANCE OUR DEVELOPMENT OF NEW THERAPIES FOR SBMA.