The long-term objective of this research program is to provide a comprehensive understanding of the biochemical mechanisms and physiological regulation of intracellular protein degradation. This objective has broad significance for understanding numerous cellular processes that utilize protein degradation as a mechanism for their regulation, and for alleviating diseases characterize by tissue atrophy. The general goal of this project is to establish the physiological role of PA28, a protein activation of the proteasome. The proteasome is an intracellular protease required for all ubiquitin-dependent-and an unknown amount of ubiquitin-independent protein degradation in eukaryotic cells. Proteasome function both in vitro and in vivo is mediated by multiple regulatory proteins whose relative cellular roles are poorly defined. PA28 is one of the least understood of these proteins. The cellular role of PA28 will be defined by over-expressing the protein in mammalian cells. These studies will test the hypothesis that PA28 increases overall rates of intracellular protein degradation. The cellular function of PA28 will be examined further by closely related biochemical experiments. These experiments will establish the role of reversible phosphorylation of PA28 as a mechanism for control of its activity by testing the hypothesis that phosphorylation of the PA28 inhibits its proteasome-stimulatory activity. The effect of PA28 on the degradation of model proteins will be studied in vitro by analyzing the kinetics of protein degradation by PA28-proteasome complexes alone and in combination with other proteasome-regulatory protein complexes. These experiments will test the hypothesis that PA28's cellular function is to promote degradation both of large peptides directly and of large peptides generated by the action of other proteasome complexes Finally, cellular substrates for the PA28 proteasome complex will be identified with a screening strategy using expression cloning. These highly integrated studies will define cellular role of PA28 and the possible biochemical bases for them. Therefore, this project will greatly increase the understanding of the mechanisms and regulation of intracellular protein degradation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK046181-05
Application #
2690694
Study Section
Biochemistry Study Section (BIO)
Program Officer
Haft, Carol R
Project Start
1994-07-01
Project End
2002-06-30
Budget Start
1998-09-10
Budget End
1999-06-30
Support Year
5
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Physiology
Type
Schools of Medicine
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
Li, Xiaohua; Thompson, David; Kumar, Brajesh et al. (2014) Molecular and cellular roles of PI31 (PSMF1) protein in regulation of proteasome function. J Biol Chem 289:17392-405
Demartino, George N (2012) Reconstitution of PA700, the 19S regulatory particle, from purified precursor complexes. Methods Mol Biol 832:443-52
Kim, Young-Chan; DeMartino, George N (2011) C termini of proteasomal ATPases play nonequivalent roles in cellular assembly of mammalian 26 S proteasome. J Biol Chem 286:26652-66
Agarwal, Anil K; Xing, Chao; DeMartino, George N et al. (2010) PSMB8 encoding the ýý5i proteasome subunit is mutated in joint contractures, muscle atrophy, microcytic anemia, and panniculitis-induced lipodystrophy syndrome. Am J Hum Genet 87:866-72
Kumar, Brajesh; Kim, Young-Chan; DeMartino, George N (2010) The C terminus of Rpt3, an ATPase subunit of PA700 (19 S) regulatory complex, is essential for 26 S proteasome assembly but not for activation. J Biol Chem 285:39523-35
Lewis, Karen A; Yaeger, Arynn; DeMartino, George N et al. (2010) Accelerated formation of alpha-synuclein oligomers by concerted action of the 20S proteasome and familial Parkinson mutations. J Bioenerg Biomembr 42:85-95
Djakovic, Stevan N; Schwarz, Lindsay A; Barylko, Barbara et al. (2009) Regulation of the proteasome by neuronal activity and calcium/calmodulin-dependent protein kinase II. J Biol Chem 284:26655-65
DeMartino, George N (2009) PUPylation: something old, something new, something borrowed, something Glu. Trends Biochem Sci 34:155-8
Thompson, David; Hakala, Kevin; DeMartino, George N (2009) Subcomplexes of PA700, the 19 S regulator of the 26 S proteasome, reveal relative roles of AAA subunits in 26 S proteasome assembly and activation and ATPase activity. J Biol Chem 284:24891-903
Ikeda, Yukio; Demartino, George N; Brown, Michael S et al. (2009) Regulated endoplasmic reticulum-associated degradation of a polytopic protein: p97 recruits proteasomes to Insig-1 before extraction from membranes. J Biol Chem 284:34889-900

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