Krause J E, Chirgwin J M, Carter M S, Xu Z S, Hershey A D
Proc Natl Acad Sci U S A. 1987 Feb;84(3):881-5. doi: 10.1073/pnas.84.3.881.
Synthetic oligonucleotides were used to screen a rat striatal cDNA library for sequences corresponding to the tachykinin peptides substance P and neurokinin A. The cDNA library was constructed from RNA isolated from the rostral portion of the rat corpus striatum, the site of striatonigral cell bodies. Two types of cDNAs were isolated and defined by restriction enzyme analysis and DNA sequencing to encode both substance P and neurokinin A. The two predicted preprotachykinin protein precursors (130 and 115 amino acids in length) differ from each other by a pentadecapeptide sequence between the two tachykinin sequences, and both precursors possess appropriate processing signals for substance P and neurokinin A production. The presence of a third preprotachykinin mRNA of minor abundance in rat striatum was established by S1 nuclease protection experiments. This mRNA encodes a preprotachykinin of 112 amino acids containing substance P but not neurokinin A. These three mRNAs are derived from one rat gene as a result of differential RNA processing; thus, this RNA processing pattern further increases the diversity of products that can be generated from the preprotachykinin gene.
合成寡核苷酸用于筛选大鼠纹状体cDNA文库,以寻找与速激肽肽P物质和神经激肽A相对应的序列。该cDNA文库由从大鼠纹状体前部(即纹状体黑质细胞体所在部位)分离的RNA构建而成。通过限制性内切酶分析和DNA测序分离并鉴定了两种类型的cDNA,它们编码P物质和神经激肽A。两种预测的前速激肽原蛋白前体(长度分别为130和115个氨基酸)在两个速激肽序列之间因一个十五肽序列而彼此不同,并且两种前体都具有用于产生P物质和神经激肽A的适当加工信号。通过S1核酸酶保护实验确定了大鼠纹状体中存在第三种低丰度的前速激肽原mRNA。该mRNA编码一个含有P物质但不含神经激肽A的112个氨基酸的前速激肽原。这三种mRNA是由于RNA的差异加工而从一个大鼠基因衍生而来;因此,这种RNA加工模式进一步增加了从前速激肽原基因产生的产物的多样性。