Takeuchi M, Fujisawa H
Department of Biochemistry, Asahikawa Medical College, Hokkaido, Japan.
Gene. 1998 Oct 9;221(1):107-15. doi: 10.1016/s0378-1119(98)00422-3.
Polymerase chain reaction analysis revealed four alternatively spliced variants of each of the gamma and delta isoforms of calmodulin-dependent protein kinase II (CaM-kinase II) in rabbit liver. Among the four variants of the gamma isoform, two were novel ones, designated as CaM-kinase II gamma-H and gamma-I. The gamma-I variant possessed both of the two deletable exons; D2a and D2b, which had never been found together in any variant. Sequence analysis of the gamma-I indicated that the D2a was upstream of the D2b and that they were contiguous with each other in the gamma-I. Among the four variants of the delta isoform, two were also novel ones, designated as CaM-kinase II delta-11 and delta-12, and the other two were the already-reported ones, delta-2 and delta-6. The delta-11 and delta-12 were identical to the delta-2 and delta-6, respectively, except that three bases (CAG) located at a splicing junction was deleted in the delta-11 and delta-12, suggesting two splicing sites of a single intron. Thus, the diverse splicing patterns may produce many more variants than those so far considered.
聚合酶链反应分析显示,兔肝脏中钙调蛋白依赖性蛋白激酶II(CaM激酶II)的γ和δ亚型各有四种可变剪接变体。在γ亚型的四种变体中,有两种是新的,分别命名为CaM激酶IIγ-H和γ-I。γ-I变体同时拥有两个可缺失外显子;D2a和D2b,在任何变体中从未同时发现过。γ-I的序列分析表明,D2a在D2b的上游,并且它们在γ-I中彼此相邻。在δ亚型的四种变体中,也有两种是新的,分别命名为CaM激酶IIδ-11和δ-12,另外两种是已报道的δ-2和δ-6。δ-11和δ-12分别与δ-2和δ-6相同,只是δ-11和δ-12在剪接连接处缺失了三个碱基(CAG),提示单个内含子的两个剪接位点。因此,多样的剪接模式可能产生比目前所认为的更多的变体。