A PHORBOL ESTER-RESPONSIVE PKC-ZETA GENERATED BY FUSION WITH THE REGULATORY DOMAIN OF PKC-DELTA

被引:15
|
作者
GOODE, NT
PARKER, PJ
机构
[1] UNIV LONDON ROYAL VET COLL, DEPT VET BASIC SCI, LONDON NW1 0TU, ENGLAND
[2] IMPERIAL CANC RES FUND, PROT PHOSPHORYLAT LAB, LONDON WC2A 3PX, ENGLAND
来源
FEBS LETTERS | 1994年 / 340卷 / 1-2期
关键词
ISOTYPE REGULATION; PHOSPHORYLATION; PROTEIN KINASE ZETA; PROTEIN KINASE CG; SUBSTRATE SPECIFICITY; SCHIZOSACCHAROMYCES POMBE;
D O I
10.1016/0014-5793(94)80190-8
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
A hybrid molecule generated by fusing the regulatory domain of PKC-delta with the catalytic domain of PKC-delta is, like PKC-delta but unlike PKC-zeta, a phorbol ester-dependent enzyme. However, the substrate specificity of this hybrid resembles that of PKC-zeta. Expression of mammalian PKC-delta, but not PKC-zeta, in the fission yeast Schizosaccharomyces pombe causes growth retardation and phorbol esters amplify the PKC-delta phenotype without affecting that of PKC-zeta (Goode et al., submitted). The chimaeric molecule also inhibited growth and this effect was phorbol-ester dependent. Both the hybrid and PKC-delta holoenzyme, in contrast to PKC-zeta, down-regulate upon prolonged exposure to phorbol esters in vivo. Thus, this hybrid retains the regulatory properties conferred by PKC-delta but the catalytic properties of PKC-zeta. This regulatable chimaeric molecule will be useful in assessing the function of PKC-zeta.
引用
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页码:145 / 150
页数:6
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