PRECURSOR OF CDK5 ACTIVATOR, THE 23-KDA SUBUNIT OF TAU-PROTEIN KINASE-II - ITS SEQUENCE AND DEVELOPMENTAL-CHANGE IN BRAIN

被引:71
作者
UCHIDA, T
ISHIGURO, K
OHNUMA, J
TAKAMATSU, M
YONEKURA, S
IMAHORI, K
机构
[1] Mitsubishi Kasei Institute of Life Sciences, Machida-shi, Tokyo, 194
关键词
CYCLIN-DEPENDENT KINASE 5; TAU PROTEIN; PAIRED HELICAL FILAMENT; ALZHEIMERS DISEASE;
D O I
10.1016/0014-5793(94)01163-X
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
Tau protein kinase II (TPKII) is shown by immunoprecipitation to be a complex composed of two subunits, a catalytic subunit, cdk5, and regulatory subunit, p23. By sequence analysis of p23 cDNA, p23 was found to occupy a region from the 99th amino acid residue to the C-terminus of a novel protein with a molecular weight of 34,000 Da, suggesting that this 34 kDa protein is a precursor of p23 (pre-p23). These findings suggest that p23 results from the processing of the precursor protein, pre-p23. The precursor mRNA was expressed most abundantly in rat brain just before and after birth. Expression of pre-p23, but not of cdk5, mRNA changed, coinciding with the developmental change of TPKII activity, suggesting that its expression controls the phosphorylation of tau by the TPKII/TPKI system in the neonatal brain, p23 appears to be a cdk5 activator in neuronal cells.
引用
收藏
页码:35 / 40
页数:6
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