Bayer K U, Löhler J, Harbers K
Heinrich-Pette-Institut für Experimentelle Virologie und Immunologie, Universität Hamburg, Germany.
Mol Cell Biol. 1996 Jan;16(1):29-36. doi: 10.1128/MCB.16.1.29.
The gene for the alpha isoform of Ca2+/calmodulin-dependent kinase II (alpha CaMKII) codes for a multifunctional protein kinase that is found exclusively in the brain. Here we show that in skeletal muscle, an alternative nonkinase product, hereafter referred to as alpha KAP (alpha CaMKII association protein), is expressed from the same gene. alpha KAP consists of a C-terminal region that is identical to the association domain of alpha CaMKII, with the exception of 11 amino acids inserted in the variable region. The N-terminal sequence of alpha KAP is highly hydrophobic and not present in any known CaMKII protein. The catalytic and regulatory domains of alpha CaMKII are missing in alpha KAP. Analysis of the exon-intron structure revealed that the alpha KAP transcript is derived from the alpha CaMKII gene by alternative promoter usage and RNA splicing. The transcriptional start site of alpha KAP mRNA is located within an intron of the alpha CaMKII gene. Therefore, the relationship between alpha KAP and alpha CaMKII is that of a gene within a gene. Immunostaining using anti-alpha KAP antibodies suggests that alpha KAP is associated with sarcomeres of skeletal muscle fibers. On the basis of its primary structure and specific location, the possible function of alpha KAP as an anchoring protein for CaMKII is discussed.
钙调蛋白依赖性蛋白激酶II(αCaMKII)α亚型的基因编码一种仅在大脑中发现的多功能蛋白激酶。在此我们表明,在骨骼肌中,一种替代性的非激酶产物,以下称为αKAP(αCaMKII结合蛋白),由同一基因表达。αKAP由一个C末端区域组成,该区域与αCaMKII的结合结构域相同,但可变区域插入了11个氨基酸。αKAP的N末端序列高度疏水,在任何已知的CaMKII蛋白中均不存在。αCaMKII的催化和调节结构域在αKAP中缺失。对外显子-内含子结构的分析表明,αKAP转录本是通过使用替代性启动子和RNA剪接从αCaMKII基因衍生而来。αKAP mRNA的转录起始位点位于αCaMKII基因的一个内含子内。因此,αKAP与αCaMKII的关系是基因内基因的关系。使用抗αKAP抗体的免疫染色表明,αKAP与骨骼肌纤维的肌节相关。基于其一级结构和特定位置,讨论了αKAP作为CaMKII锚定蛋白的可能功能。