Fraser P J, Curtis P J
J Mol Evol. 1986;23(4):294-9. doi: 10.1007/BF02100637.
A cDNA clone in pBR322 that cross-hybridizes with a mouse carbonic anhydrase form II (CAII) probe has been sequenced and identified as mouse carbonic anhydrase form I (CAI). The 1224-base-pair clone encodes the entire 260-amino-acid protein and appears to contain an Alu-like element in the 3' untranslated region. The deduced amino acid sequence exhibits 77% homology to human CAI and contains 17 of the 20 residues that are considered unique to and invariant for all mammalian CAI isozymes. The results of a detailed comparison of the nucleic acid sequences spanning the coding regions of mouse CAI and rabbit CAI have been used to calibrate an evolutionary clock for the carbonic anhydrases (CAs). These data have been applied to a comparison of the mouse CAI and CAII nucleic acid sequences to calculate the divergence time between the two genes. The divergence-time calculation provides the first estimation of the evolutionary relationship between CAs based entirely on nucleotide sequence comparison.
一个与小鼠碳酸酐酶II型(CAII)探针发生交叉杂交的pBR322 cDNA克隆已被测序,并鉴定为小鼠碳酸酐酶I型(CAI)。这个1224个碱基对的克隆编码了完整的260个氨基酸的蛋白质,并且在3'非翻译区似乎含有一个类似Alu的元件。推导的氨基酸序列与人类CAI具有77%的同源性,并且包含了所有哺乳动物CAI同工酶特有的20个残基中的17个。跨越小鼠CAI和兔CAI编码区的核酸序列的详细比较结果已被用于校准碳酸酐酶(CAs)的进化时钟。这些数据已被应用于小鼠CAI和CAII核酸序列的比较,以计算这两个基因之间的分歧时间。分歧时间的计算提供了完全基于核苷酸序列比较对CAs之间进化关系的首次估计。