Bacher N, Zisman Y, Berent E, Livneh E
Department of Chemical Immunology, Weizmann Institute of Science, Rehovot, Israel.
Mol Cell Biol. 1991 Jan;11(1):126-33. doi: 10.1128/mcb.11.1.126-133.1991.
We have isolated and characterized a new human cDNA, coding for a protein kinase, related to the protein kinase C (PKC) gene family. Although this protein kinase shares some homologous sequences and structural features with the four members of the PKC family initially isolated (alpha, beta I, beta II, and gamma), it shows more homology with the recently described PKC-related subfamily, encoded by the cDNAs delta, epsilon, and zeta. The transcript for this gene product, termed PKC-L, is most abundant in lung tissue, less expressed in heart and skin tissue, and exhibited very low expression in brain tissue. Thus, its tissue distribution is different from that described for other mammalian members of the PKC gene family, their expression being enriched in brain tissues. PKC-L is also expressed in several human cell lines, including the human epidermoid carcinoma line A431. The ability of phorbol esters to bind to and stimulate the kinase activity of PKC-L was revealed by introducing the cDNA into COS cells.
我们已分离并鉴定出一种新的人类cDNA,它编码一种与蛋白激酶C(PKC)基因家族相关的蛋白激酶。尽管这种蛋白激酶与最初分离出的PKC家族的四个成员(α、βI、βII和γ)具有一些同源序列和结构特征,但它与最近描述的由cDNA δ、ε和ζ编码的PKC相关亚家族具有更高的同源性。这种基因产物的转录本称为PKC-L,在肺组织中最为丰富,在心脏和皮肤组织中表达较少,而在脑组织中表达极低。因此,其组织分布与PKC基因家族的其他哺乳动物成员不同,它们在脑组织中的表达更为丰富。PKC-L也在几种人类细胞系中表达,包括人表皮样癌细胞系A431。通过将cDNA导入COS细胞,发现佛波酯能够结合并刺激PKC-L的激酶活性。