P53S DIRECT ROLE IN MITOCHONDRIAL CONTROL OF APOPTOSIS
P53S DIRECT ROLE IN MITOCHONDRIAL CONTROL OF APOPTOSIS
批准号:
6489260
负责人:
UTE Martha MOLL
金额:
$21.78万
依托单位国家:
美国
项目类别:
财政年份:
1993
资助国家:
美国
项目状态:
已结题
起止时间:
1993-09-15 至 2003-12-31
关键词:
Baculoviridae acetylation apoptosis cell line confocal scanning microscopy genetic regulation genetic transcription immunoelectron microscopy immunoprecipitation laboratory mouse mitochondria molecular site myelogenous leukemia neuroblastoma phosphorylation protein localization protein protein interaction stress proteins tissue /cell culture tumor suppressor proteins
中文摘要
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英文摘要
DESCRIPTION: (adapted from the investigator's abstract)
The mechanism of p53-mediated apoptosis remains poorly understood.
Current evidence suggests that p53 induces cell death by separate
transcription-dependent and -independent pathways. Mitochondrial
involvement is critical for most forms of cell death. Data from the
investigator's laboratory suggests that in cells with an intact p53-
mediated apoptotic pathway, p53 protein is physically present within the
mitochondria in a specific low-abundance protein complex with mt-hsp 70.
Mt-hsp70 likely mediates mitochondrial import and refolding of p53. This
apparent organellar location strongly argues for a direct transcription-
independent regulatory role of p53 in the mitochondrial phase of
apoptosis. In contrast, neuroblastoma cells which are resistant to
apoptosis under the conditions tested, appear to contain abnormally high
(deregulated) levels of mitochondrial p53/mt-hsp70 complexes, associated
with covalent modification of p53. This suggests an altered function of
p53 which may result in an anti-apoptotic phenotype at the mitochondrial
level in this tumor. Biochemical and genetic experiments addressing the
functional significance of p53's presence within mitochondria under
physiological conditions are the core of this proposal.
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