Kronenberg H M, McDevitt B E, Majzoub J A, Nathans J, Sharp P A, Potts J T, Rich A
Proc Natl Acad Sci U S A. 1979 Oct;76(10):4981-5. doi: 10.1073/pnas.76.10.4981.
We have cloned in Escherichia coli a DNA copy of mRNA coding for bovine preproparathyroid hormone. Double-stranded DNA was inserted into the Pst I site in plasmid pBR322 by using the poly(dG)-poly(dC) homopolymer extension technique to join the DNA molecules. Recombinant plasmids coding for preproparathyroid hormone were identified by the plasmid's ability to arrest specifically the translation of preproparathyroid hormone mRNA. The nucleotide sequence of the largest recombinant was determined by using both chemical and enzymatic techniques. The parathyroid insert contains 470 nucleotides--102 nucleotides from the 5' noncoding region of the mRNA, 345 nucleotides representing the entire coding region, and 23 nucleotides from the 3' noncoding region. The coding sequence clarifies the hormone's amino acid sequence, which has been disputed. Codon usage is discussed.
我们已在大肠杆菌中克隆出编码牛甲状旁腺激素原前体的信使核糖核酸(mRNA)的DNA拷贝。利用聚(dG)-聚(dC)同聚物延伸技术将双链DNA插入质粒pBR322的Pst I位点,以连接DNA分子。通过质粒特异性阻止甲状旁腺激素原前体mRNA翻译的能力来鉴定编码甲状旁腺激素原前体的重组质粒。利用化学和酶促技术确定了最大重组体的核苷酸序列。甲状旁腺插入片段包含470个核苷酸——来自mRNA 5'非编码区的102个核苷酸、代表整个编码区的345个核苷酸以及来自3'非编码区的23个核苷酸。编码序列阐明了存在争议的该激素的氨基酸序列。文中还讨论了密码子的使用情况。