Harris T J, Lowe P A, Lyons A, Thomas P G, Eaton M A, Millican T A, Patel T P, Bose C C, Carey N H, Doel M T
Nucleic Acids Res. 1982 Apr 10;10(7):2177-87. doi: 10.1093/nar/10.7.2177.
DNA complementary to calf stomach mRNA has been synthesised and inserted into the Pst1 site of pAT153 by G-C tailing. Clones containing sequences coding for prochymosin were recognised by colony hybridisation with cDNA extended from a chemically synthesised oligodeoxynucleotide primer, the sequence of which was predicted from the published amino acid sequence of calf prochymosin. Two clones were identified which together contained a complete copy of prochymosin mRNA. The nucleotide sequence is in substantial agreement with the reported amino acid sequence of prochymosin and shows that this protein has a mol.wt. of 40431 and chymosin a mol.wt. of 35612. The sequence also indicates that prochymosin is synthesised as a precursor molecule, preprochymosin, having a 16 amino acid hydrophobic leader sequence analogous to that reported for other secreted proteins.
已通过G-C加尾法合成了与小牛胃mRNA互补的DNA,并将其插入到pAT153的Pst1位点。通过与从化学合成的寡脱氧核苷酸引物延伸而来的cDNA进行菌落杂交,识别出含有编码前凝乳酶序列的克隆,该引物的序列是根据已发表的小牛前凝乳酶氨基酸序列预测的。鉴定出两个克隆,它们共同包含前凝乳酶mRNA的完整拷贝。核苷酸序列与报道的前凝乳酶氨基酸序列基本一致,表明该蛋白质的分子量为40431,凝乳酶的分子量为35612。该序列还表明,前凝乳酶作为前体分子前原凝乳酶被合成,具有16个氨基酸的疏水前导序列,类似于其他分泌蛋白报道的序列。