Billadello J J, Kelly D P, Roman D G, Strauss A W
Biochem Biophys Res Commun. 1986 Jul 16;138(1):392-8. doi: 10.1016/0006-291x(86)90294-9.
To define the structure of canine B creatine kinase, clones were isolated from a library prepared from dog brain mRNA and constructed in the vector lambda gt11. The entire coding portion, the complete 3' nontranslated region, and 43 bp of the 5' noncoding region are reported. Comparison of the predicted amino acid sequence of canine B creatine kinase with the sequence of canine M creatine kinase shows 81% identity. When compared to cDNAS encoding B creatine kinase isolated form other species unusual and striking nucleotide sequence identity in the 3' noncoding region is present. Moreover, two B creatine kinase clones (BCK2 and BCK38) demonstrate microheterogeneity within the 3' nontranslated region indicating variable processing of B creatine kinase pre-mRNA or the existence of multiple genes encoding canine B creatine kinase.
为了确定犬B型肌酸激酶的结构,从以狗脑mRNA构建的文库中分离出克隆,并构建于λgt11载体中。报道了整个编码部分、完整的3'非翻译区以及5'非编码区的43个碱基对。犬B型肌酸激酶预测的氨基酸序列与犬M型肌酸激酶序列比较显示81%的同一性。与从其他物种分离的编码B型肌酸激酶的cDNA相比,在3'非编码区存在异常且显著的核苷酸序列同一性。此外,两个B型肌酸激酶克隆(BCK2和BCK38)在3'非翻译区内表现出微异质性,表明B型肌酸激酶前体mRNA的可变加工或存在多个编码犬B型肌酸激酶的基因。