Wirz T, Brändle U, Soldati T, Hossle J P, Perriard J C
Institute for Cell Biology, Swiss Federal Institute of Technology, Zurich.
J Biol Chem. 1990 Jul 15;265(20):11656-66.
In the chicken, a high degree of heterogeneity at the protein level has been reported for the creatine kinase-type B (B-CK). Here we show that the two B-CK isoproteins, Ba- and Bb-CK, are encoded by two mRNAs, which are derived from a single copy gene by a stochastic alternative splicing mechanism. The transcription of the single hnRNA is directed by a complex promoter region containing a stretch of sequences which is highly conserved among all the B-CK genes known to date. This stretch encompasses a putative binding site for the TA-rich DNA-binding protein (Hobson, G. M., Mitchell, M. T., Molloy, G. R., and Pearson, M. L. (1988) Nucleic Acids Res. 16, 8925-8944) which is located in the distal part of the promoter region, while the proximal portion containing the TATA-box used in vivo is not conserved between chicken and mammals. The two isoproteins arising from this gene contain distinct N-terminal portions. According to comparative analysis, Bb-CK is the form which is homologous to the mammalian B-CKs, whereas Ba-CK shows some sequence features unique among all other vertebrate cytosolic creatine kinases characterized so far.
在鸡中,已报道肌酸激酶B型(B-CK)在蛋白质水平上具有高度异质性。在此我们表明,两种B-CK同工酶,即Ba-CK和Bb-CK,由两种mRNA编码,这两种mRNA通过随机可变剪接机制源自单个拷贝基因。单个核不均一RNA(hnRNA)的转录由一个复杂的启动子区域指导,该区域包含一段在迄今为止已知的所有B-CK基因中高度保守的序列。这段序列包含一个富含TA的DNA结合蛋白的假定结合位点(霍布森,G.M.,米切尔,M.T.,莫洛伊,G.R.,和皮尔逊,M.L.(1988年)核酸研究16,8925 - 8944),其位于启动子区域的远端部分,而鸡和哺乳动物之间在体内使用的含TATA框的近端部分并不保守。由该基因产生的两种同工酶含有不同的N末端部分。根据比较分析,Bb-CK是与哺乳动物B-CK同源的形式,而Ba-CK在迄今为止所表征的所有其他脊椎动物胞质肌酸激酶中显示出一些独特的序列特征。