Minth C D, Taylor W L, Magazin M, Tavianini M A, Collier K, Weith H L, Dixon J E
J Biol Chem. 1982 Sep 10;257(17):10372-7.
Pancreatic poly(A) RNA isolated from the channel catfish (Ictalurus punctatus) was enriched for sequences corresponding to somatostatin mRNA on isokinetic sucrose gradients. Double-stranded cDNA was synthesized and inserted into the Pst I site pBR322 via the poly(dG) . poly(dC) tailing method. Escherichia coli was transformed with this DNA, and colonies containing somatostatin cDNA sequences were identified by hybridization using a primer-extended somatostatin cDNA. The somatostatin cDNA was obtained by extending a 5'-labeled undecanucleotide primer complementary to somatostatin mRNA with reverse transcriptase using catfish poly(A) RNA as a template. The synthetic primer d(T-T-C-C-A-G-A-A-G-A-A) was deduced from the amino acid sequence Phe-Phe-Trp-Lys present in somatostatin-14. Twenty positive colonies were obtained upon screening 2000 transformants. The restriction maps of the plasmid DNA obtained from the positive colonies were examined. Nineteen of these plasmids contained sequences corresponding to somatostatin-14, while one contained a sequence corresponding to somatostatin-22. The nucleotide sequence of pancreatic somatostatin-14 is reported here. The cDNA contains 350 nucleotides in the 3' noncoding region, 345 nucleotides in the coding region, and 104 nucleotides in the 5'-untranslated region. The mRNA codes for a precursor to somatostatin which is 114 amino acids in length. The preprosomatostatin has a sequence of hydrophobic amino acids at the NH2 terminus, followed by a connecting peptide of approximately 75 amino acids. The sequence Arg-Lys precedes somatostatin-14. Analysis of genomic DNA from the channel catfish reveals that somatostatin-14 and somatostatin-22 are present on different restriction fragments.
从斑点叉尾鮰(Ictalurus punctatus)分离出的胰腺多聚腺苷酸RNA在等密度蔗糖梯度上富集了与生长抑素mRNA相对应的序列。通过聚(dG)·聚(dC)加尾法合成双链cDNA,并将其插入pBR322的Pst I位点。用该DNA转化大肠杆菌,使用引物延伸的生长抑素cDNA通过杂交鉴定含有生长抑素cDNA序列的菌落。生长抑素cDNA是通过以斑点叉尾鮰多聚腺苷酸RNA为模板,用逆转录酶延伸与生长抑素mRNA互补的5'-标记的十一核苷酸引物获得的。合成引物d(T-T-C-C-A-G-A-A-G-A-A)是根据生长抑素-14中存在的氨基酸序列苯丙氨酸-苯丙氨酸-色氨酸-赖氨酸推导出来的。筛选2000个转化体后获得了20个阳性菌落。检查了从阳性菌落获得的质粒DNA的限制性图谱。这些质粒中有19个含有与生长抑素-14相对应的序列,而1个含有与生长抑素-22相对应的序列。这里报道了胰腺生长抑素-14的核苷酸序列。该cDNA在3'非编码区含有350个核苷酸,在编码区含有345个核苷酸,在5'-非翻译区含有104个核苷酸。该mRNA编码一种长度为114个氨基酸的生长抑素前体。前生长抑素原在NH2末端有一段疏水氨基酸序列,后面跟着一段约75个氨基酸的连接肽。精氨酸-赖氨酸序列在生长抑素-14之前。对斑点叉尾鮰基因组DNA的分析表明,生长抑素-14和生长抑素-22存在于不同的限制性片段上。