Giraudat J, Devillers-Thiery A, Perriard J C, Changeux J P
Proc Natl Acad Sci U S A. 1984 Dec;81(23):7313-7. doi: 10.1073/pnas.81.23.7313.
DNA sequences coding for the muscle-specific subunit of creatine kinase have been isolated from cDNA libraries constructed from Torpedo marmorata electric organ. Clones were screened by differential in situ hybridization and hybrid-selected translation. The in vitro translation product of the selected mRNA was immunoprecipitated by anti-chicken creatine kinase antibodies and comigrated with Torpedo muscle creatine kinase on two-dimensional gels at the same position as the cytosolic 43,000-dalton protein referred to as nu 2. The cDNA inserts hybridized to a mRNA species present in adult Torpedo muscle but not in brain. The complete sequence of the mRNA was determined on one of the clones except for the 78 nucleotides of the mRNA 5' terminal sequence, which were identified by the primer extension method. The amino acid sequence of muscle-specific creatine kinase from T. marmorata was deduced and analyzed. It includes the known sequence of a peptide from the active site of rabbit muscle-specific creatine kinase.
编码肌酸激酶肌肉特异性亚基的DNA序列已从用斑电鳐电器官构建的cDNA文库中分离出来。通过差异原位杂交和杂交选择翻译筛选克隆。所选mRNA的体外翻译产物用抗鸡肌酸激酶抗体进行免疫沉淀,并在二维凝胶上与斑电鳐肌肉肌酸激酶共迁移,位于与称为nu 2的43000道尔顿胞质蛋白相同的位置。cDNA插入片段与成年斑电鳐肌肉中存在但脑中不存在的一种mRNA杂交。除了通过引物延伸法鉴定的mRNA 5'末端序列的78个核苷酸外,在其中一个克隆上确定了mRNA的完整序列。推导并分析了斑电鳐肌肉特异性肌酸激酶的氨基酸序列。它包括来自兔肌肉特异性肌酸激酶活性位点的一个肽段的已知序列。