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MECHANICS AND FUNCTIONS OF THE N-END RULE PATHWAY

MECHANICS AND FUNCTIONS OF THE N-END RULE PATHWAY
N 端规则路径的机制和功能
批准号:
6350653
负责人:
ALEXANDER J VARSHAVSKY
金额:
$43.3万
依托单位国家:
美国
项目类别:
财政年份:
1988
资助国家:
美国
项目状态:
已结题
起止时间:
1988-02-01 至 2003-01-31

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DESCRIPTION: Ubiquitin is a 76-residue protein that exists in cells either free or conjugated to many other proteins. Selective degradation of proteins by the ubiquitin/proteasome-dependent pathways plays a role in a multitude of biological processes, including cell growth and differentiation, signal transduction and responses to stress. One ubiquitin/proteasome-dependent proteolytic system is the N-end rule pathway, identified by the laboratory in 1986. The N-end rule relates the in vivo half-life of a protein to the identity of its N-terminal residue. The N-end rule pathway is present in all organisms examined, from mammals to bacteria. Studies supported by the present grant ("Mechanics and Functions of the N-end Rule Pathway", DK39520), currently in its 11th year, have yielded significant insights into the N-end rule's functions and mechanisms, as described in the Progress Report. The objective of the research described in this renewal application is to advance the understanding of the N-end rule pathway and related aspects of the ubiquitin system. Specific aims are: 1) Regulation of peptide import by the N-end rule pathway: biochemical and genetic studies; 2) A fusion-based screen for physiological substrates of the N-end rule pathway in S. cerevisiae; 3) Isolation and analysis of regulators of the N-end rule pathway; 4) Screens for mutants whose viability requires the presence of the N-end r; 5) The use of suppression subtractive hybridization to identify new functions of the N-end rule pathway; 6) Analysis of a mitochondrial function of the Ntalp N-terminal amidase in S. cerevisiae; 7) A biochemico-genetic approach to identification of physiological N-end rule substrates; 8) A "double-headed" inhibitor of the N-end rule pathway; 9) The "two-ubiquitin" technique and its application to the problem of cotranslational proteolysis; and 10) Biochemical and genetic dissection of the UBRI-encoded Nrecognin and Ubr2p, a recently identified homolog of Ubrlp in S. cerevisiae.
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Ubiquitin Ligases, Mechanisms and Functions of the N-End Rule Pathway
  • 批准号:
    7996378
  • 项目类别:
  • 资助金额:
    $2.8万
  • 财政年份:
    2009
  • 负责人:
    ALEXANDER J VARSHAVSKY
  • 依托单位:
Split Proteins As Boolean Circuits and Drugs of a New Kind
  • 批准号:
    7513269
  • 项目类别:
  • 资助金额:
    $32.1万
  • 财政年份:
    2008
  • 负责人:
    ALEXANDER J VARSHAVSKY
  • 依托单位:
Split Proteins As Boolean Circuits and Drugs of a New Kind
  • 批准号:
    8118431
  • 项目类别:
  • 资助金额:
    $31.46万
  • 财政年份:
    2008
  • 负责人:
    ALEXANDER J VARSHAVSKY
  • 依托单位:
Split Proteins As Boolean Circuits and Drugs of a New Kind
  • 批准号:
    7661504
  • 项目类别:
  • 资助金额:
    $32.1万
  • 财政年份:
    2008
  • 负责人:
    ALEXANDER J VARSHAVSKY
  • 依托单位:
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