Lloyd J, McMillan S, Hopkinson D, Edwards Y H
Gene. 1986;41(2-3):233-9. doi: 10.1016/0378-1119(86)90103-4.
We report the nucleotide (nt) sequence of a full length cDNA clone, pCA15, which encodes the human muscle-specific carbonic anhydrase, CAIII. pCA15 identifies a 1.7-kb mRNA, which is present at high levels in skeletal muscle, at much lower levels in cardiac and smooth muscle and which appears to be developmentally regulated. The CAIII mRNA is distinguished by a 887-nt long 3'-untranslated region, containing two AAUAAA signal sequences and is longer than either of the mRNAs encoding the erythrocyte CAs, CAI and CAII, which each have relatively shorter 3'-untranslated regions, 360 and 670 nt long, respectively. The derived amino acid (aa) sequence for human CAIII shows 85% homology with ox CAIII, 62% homology with human CAII and 54% with human CAI when simple pairwise aa comparisons are made. We describe an allelic variation at a TaqI restriction site for CAIII which occurs at high frequency in the European population.
我们报道了一个全长cDNA克隆pCA15的核苷酸(nt)序列,它编码人类肌肉特异性碳酸酐酶CAIII。pCA15鉴定出一种1.7kb的mRNA,其在骨骼肌中高水平存在,在心肌和平滑肌中水平低得多,并且似乎受发育调控。CAIII mRNA的特征是其3'非翻译区长887nt,包含两个AAUAAA信号序列,并且比编码红细胞碳酸酐酶CAI和CAII的任何一种mRNA都长,后两者的3'非翻译区相对较短,分别为360nt和670nt长。当进行简单的氨基酸两两比较时,推导的人类CAIII氨基酸(aa)序列与牛CAIII显示85%的同源性,与人类CAII显示62%的同源性,与人类CAI显示54%的同源性。我们描述了CAIII在TaqI限制性位点的一个等位基因变异,该变异在欧洲人群中高频出现。