Regulated proteolysis is used to drive many biological processes, including the cell cycle, cell death, and embryonic patterning. It is also thought to mediate complex brain functions such as learning and memory. Not surprisingly, then, defects in regulated proteolysis lead to human pathologies such as cancer and neurodegenerative disease. The overall goal of this grant is to understand the mechanisms of regulated proteolysis involving the coordinated action of serine proteases and their inhibitors called serpins.
Three specific aims are proposed: 1) To test the hypothesis that a serpin is an inhibitor of proconvertases, serine proteases that activate a wide range of cellular and pathogenic proteins, including hormones, growth factors, and virulence determinants. 2) To identity serine proteases involved in the melanization reaction, an insect analogue of the mammalian blood clotting reaction and a critical determinant of malarial resistance in the mosquito. 3) To perform an RNAi-based screen for serpin function that ultimately will lead to the identification of new biological processes involving serine proteases and serpins. These studies will exploit Drosophila, which utilizes many of the same molecular and cellular mechanisms as mammals, to learn general principles of how regulated proteolysis involving serine proteases and serpins is used for diverse biological purposes.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM049370-15
Application #
7324774
Study Section
Cell Development and Function Integrated Review Group (CDF)
Program Officer
Ikeda, Richard A
Project Start
1992-08-01
Project End
2010-11-30
Budget Start
2007-12-01
Budget End
2010-11-30
Support Year
15
Fiscal Year
2008
Total Cost
$348,812
Indirect Cost
Name
Yale University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
Hyun, Joogyung; Hashimoto, Carl (2011) Physiological effects of manipulating the level of insulin-degrading enzyme in insulin-producing cells of Drosophila. Fly (Austin) 5:53-7
Tang, Huaping (2009) Regulation and function of the melanization reaction in Drosophila. Fly (Austin) 3:105-11
Scherfer, Christoph; Tang, Huaping; Kambris, Zakaria et al. (2008) Drosophila Serpin-28D regulates hemolymph phenoloxidase activity and adult pigmentation. Dev Biol 323:189-96
Tang, Huaping; Kambris, Zakaria; Lemaitre, Bruno et al. (2008) A serpin that regulates immune melanization in the respiratory system of Drosophila. Dev Cell 15:617-26
Jang, In-Hwan; Chosa, Naoyuki; Kim, Sung-Hee et al. (2006) A Spatzle-processing enzyme required for toll signaling activation in Drosophila innate immunity. Dev Cell 10:45-55
Tang, Huaping; Kambris, Zakaria; Lemaitre, Bruno et al. (2006) Two proteases defining a melanization cascade in the immune system of Drosophila. J Biol Chem 281:28097-104
Richer, Martin J; Juliano, Luiz; Hashimoto, Carl et al. (2004) Serpin mechanism of hepatitis C virus nonstructural 3 (NS3) protease inhibition: induced fit as a mechanism for narrow specificity. J Biol Chem 279:10222-7
Richer, Martin J; Keays, Clairessa A; Waterhouse, Jennifer et al. (2004) The Spn4 gene of Drosophila encodes a potent furin-directed secretory pathway serpin. Proc Natl Acad Sci U S A 101:10560-5
Hashimoto, Carl; Kim, Dong Ryoung; Weiss, Linnea A et al. (2003) Spatial regulation of developmental signaling by a serpin. Dev Cell 5:945-50
Turcotte, Cynthia L; Hashimoto, Carl (2002) Evidence for a glycosaminoglycan on the nudel protein important for dorsoventral patterning of the drosophila embryo. Dev Dyn 224:51-7

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