One function of ubiquitin, a highly conserved 76-residue protein, is to serve as a signal for degradation of conjugated acceptor proteins. More recent work [1] has identified another,""""""""chaperone"""""""" function of ubiquitin, in which its covalent association with other proteins promotes formation of specific cellular structures [1]. Studies of the last several years, and in particular studies supported by the present grant, have demonstrated the involvement of ubiquitin-dependent processes in a remarkably broad range of cellular functions, from protein degradation and maturation to cell cycle control, stress response and DNA repair. The objective of the research described in this renewal application is to advance the understanding of the ubiquitin system.
Specific Aims : 1) Molecular genetic analysis of the yeast (S. cerevisiae) Ub-activating enzyme (E1, encoded by the UBA1 gene), and the use of conditional ubal mutants to test Ub involvement in the degradation of specific short-lived proteins. 2) Molecular genetic analysis of the yeast Ub-conjugating enzymies (E2's, encoded by the UBC1-UBC8 genes), and identification of E2's that function in the N-end rule pathway of protein degradation. 3) Studies on Ub-related aspects of the yeast N-end-recognizing protein (E3) encoded by the UBR1 gene. 4) Molecular genetic analysis of the yeast Ub-specific proteases (encoded by UBP genes) that cleave Ub off its linear or branched conjugates with itself or other proteins. 5) Using non-deubiquitinatable Ub fusions (Ub-Pro-Betagal or (Ub-Val76)-Met-Betagal) to dissect a proteolytic pathway that recognizes a single Ub moiety as degradation signal and is distinct from the N-end rule pathway. 6) Construction of Ub bearing a peptide tag, and its use to detect and identify specific constitutive and stress-inducible Ub conjugates in S. cerevisiae. 7) Further biochemical and genetic analyses of the in vivo ubiquitination and degradation of the yeast MATAlpha2 repressor. 8) Cloning and functional analysis of mammalian (mouse) genes that encode Ub-related components of the N-end rule pathway.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM031530-13
Application #
2176163
Study Section
Biochemistry Study Section (BIO)
Project Start
1992-07-01
Project End
1995-03-31
Budget Start
1994-04-01
Budget End
1995-03-31
Support Year
13
Fiscal Year
1994
Total Cost
Indirect Cost
Name
California Institute of Technology
Department
Type
Schools of Arts and Sciences
DUNS #
078731668
City
Pasadena
State
CA
Country
United States
Zip Code
91125
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Chen, Shun-Jia; Wu, Xia; Wadas, Brandon et al. (2017) An N-end rule pathway that recognizes proline and destroys gluconeogenic enzymes. Science 355:
Oh, Jang-Hyun; Chen, Shun-Jia; Varshavsky, Alexander (2017) A reference-based protein degradation assay without global translation inhibitors. J Biol Chem 292:21457-21465
Oh, Jang-Hyun; Hyun, Ju-Yeon; Varshavsky, Alexander (2017) Control of Hsp90 chaperone and its clients by N-terminal acetylation and the N-end rule pathway. Proc Natl Acad Sci U S A 114:E4370-E4379
Wadas, Brandon; Piatkov, Konstantin I; Brower, Christopher S et al. (2016) Analyzing N-terminal Arginylation through the Use of Peptide Arrays and Degradation Assays. J Biol Chem 291:20976-20992
Liu, Yu-Jiao; Liu, Chao; Chang, ZeNan et al. (2016) Degradation of the Separase-cleaved Rec8, a Meiotic Cohesin Subunit, by the N-end Rule Pathway. J Biol Chem 291:7426-38
Wadas, Brandon; Borjigin, Jimo; Huang, Zheping et al. (2016) Degradation of Serotonin N-Acetyltransferase, a Circadian Regulator, by the N-end Rule Pathway. J Biol Chem 291:17178-96
Piatkov, Konstantin I; Vu, Tri T M; Hwang, Cheol-Sang et al. (2015) Formyl-methionine as a degradation signal at the N-termini of bacterial proteins. Microb Cell 2:376-393
Park, Sang-Eun; Kim, Jeong-Mok; Seok, Ok-Hee et al. (2015) Control of mammalian G protein signaling by N-terminal acetylation and the N-end rule pathway. Science 347:1249-1252
Varshavsky, Alexander (2014) Discovery of the biology of the ubiquitin system. JAMA 311:1969-70

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