UBIQUITIN-MEDIATED DEGRADATIVE PATHWAY DEGRADES THE EXTRACELLULAR BUT NOT THE INTRACELLULAR FORM OF AMYLOID BETA-PROTEIN PRECURSOR

被引:15
作者
GREGORI, L [1 ]
BHASIN, R [1 ]
GOLDGABER, D [1 ]
机构
[1] SUNY STONY BROOK,DEPT PSYCHIAT & BEHAV SCI,STONY BROOK,NY 11794
关键词
D O I
10.1006/bbrc.1994.2386
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The presence of ubiquitin and ubiquitin conjugates has been detected in patients affected by neurodegenerative diseases such as Alzheimer's disease. We investigated the role of ubiquitin in the degradation of amyloid beta-protein precursor (APP) and its process of amyloid beta-protein formation. APP was tested as a substrate for degradation, using both the extracellular and the intracellular forms of APP(770), APP(751) and APP(695). The intracellular APP forms did not show appreciable ubiquitin-mediated degradation. In contrast, the three extracellular forms of APP were degraded in vitro by this proteolytic pathway, with similar degradation rates. Our results suggest a potential regulatory role for the ubiquitin-dependent degradation mechanism in the in vivo APP metabolic pathway. (C) 1994 Academic Press, Inc.
引用
收藏
页码:1731 / 1738
页数:8
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