PROTEIN-KINASE-C (PKC)-INDUCED PKC DOWN-REGULATION - ASSOCIATION WITH UP-REGULATION OF VESICLE TRAFFIC

被引:49
作者
GOODE, NT
HAJIBAGHERI, MAN
PARKER, PJ
机构
[1] IMPERIAL CANC RES FUND, ELECTRON MICROSCOPY UNIT, LONDON WC2A 3PX, ENGLAND
[2] IMPERIAL CANC RES FUND, PROT PHOSPHORYLAT LAB, LONDON WC2A 3PX, ENGLAND
关键词
D O I
10.1074/jbc.270.6.2669
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
Phorbol esters cause long term activation of protein kinase C (PKC) and frequently the down-regulation of PKC protein levels in mammalian cells. Mammalian PKC-gamma, -delta, and -eta down-regulate in response to phorbol esters when expressed in Schizosaccharomyces pombe. However, PKC-epsilon does not down-regulate in S. pombe, in contrast to the behavior of this isotype in mammalian cells. Go-expression of PKC-gamma or -delta with PKC-epsilon in S. pombe renders PKC-epsilon susceptible to down-regulation. A protein kinase defective form of PKC-delta does not downregulate efficiently in S. pombe but, like PKC-epsilon, is susceptible when co-expressed with PKC-gamma or full-length PKC-delta. Thus, down-regulation is a consequence of the catalytic function of certain PKC isotypes with other isotypes being affected in trans, PKC down-regulation parallels a striking accumulation of Vesicles in S. pombe, suggesting a direct relationship between these events.
引用
收藏
页码:2669 / 2673
页数:5
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