Zhu Ling, Brodie Chaya, Balasubramanian Sivaprakasam, Eckert Richard L
Department of Physiology, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
J Invest Dermatol. 2008 Apr;128(4):833-45. doi: 10.1038/sj.jid.5701103. Epub 2007 Oct 18.
Protein kinase C-delta (PKCdelta) is a key regulator of human involucrin (hINV) gene expression and is regulated by tyrosine phosphorylation. However, a comprehensive analysis of the requirement for individual PKCdelta tyrosine residues is lacking. We show that multiple tyrosine residues influence the ability of PKCdelta to increase hINV gene expression. Mutation of individual PKCdelta tyrosine residues 52, 64, 155, 187, or 565 does not reduce the ability of PKCdelta to increase hINV promoter activity; however, simultaneous mutation of these five tyrosines markedly reduces activity. Moreover, restoration of any one of these residues results in nearly full activity restoration. It is significant that phosphorylation of PKCdelta-Y(311) is reduced in the five-tyrosine mutant and that mutation of Y(311) results in reduced PKCdelta activity comparable to that observed in the five-tyrosine mutant. Restoration of any one of the tyrosine residues in the five-tyrosine mutant restores Y(311) phosphorylation and biological activity. In addition, reduced phosphorylation of endogenous PKCdelta-Y(311) is associated with reduced biological activity. These findings indicate that PKCdelta activity requires Y(311) and a second tyrosine residue; however, any one of the several tyrosine residues can serve in the secondary role.
蛋白激酶C-δ(PKCδ)是人类兜甲蛋白(hINV)基因表达的关键调节因子,且受酪氨酸磷酸化调控。然而,目前缺乏对PKCδ单个酪氨酸残基需求的全面分析。我们发现多个酪氨酸残基会影响PKCδ增加hINV基因表达的能力。PKCδ的单个酪氨酸残基52、64、155、187或565发生突变,并不会降低PKCδ增加hINV启动子活性的能力;然而,这五个酪氨酸同时发生突变则会显著降低活性。此外,恢复其中任何一个残基的功能都会使活性几乎完全恢复。值得注意的是,在五个酪氨酸突变体中PKCδ-Y(311)的磷酸化水平降低,并且Y(311)发生突变会导致PKCδ活性降低,这与在五个酪氨酸突变体中观察到的情况相当。恢复五个酪氨酸突变体中的任何一个酪氨酸残基都会恢复Y(311)的磷酸化和生物学活性。此外,内源性PKCδ-Y(311)的磷酸化水平降低与生物学活性降低相关。这些发现表明,PKCδ活性需要Y(311)和另一个酪氨酸残基;然而,几个酪氨酸残基中的任何一个都可以起到次要作用。