Perreault J P, Pon R T, Jiang M Y, Usman N, Pika J, Ogilvie K K, Cedergren R
Département de Biochimie, Université de Montréal, Canada.
Eur J Biochem. 1989 Dec 8;186(1-2):87-93. doi: 10.1111/j.1432-1033.1989.tb15181.x.
Stepwise, solid-phase chemical synthesis has provided long RNA and DNA polymers related to the sequence of Escherichia coli tRNA(fMet). The 34-ribonucleotide oligomer corresponding to the sequence of the 5'-half tRNA molecule has been synthesized and then characterized by gel purification, terminal nucleotide determinations and sequence analysis. This 34-nucleotide oligomer serves as an acceptor in the RNA-ligase-catalyzed reaction with a phosphorylated 43-ribonucleotide oligomer corresponding to the sequence of the 3'-half molecule of tRNA(fMet). The DNA molecule having the sequence of tRNA(fMet) is a 76-deoxyribonucleotide oligomer with a 3'-terminal riboadenosine residue and all U residues replaced by T. These polymers have been compared with an oligodeoxyribonucleotide lacking all 2'-hydroxyl groups except for the 3'-terminal 2'-OH, an oligoribonucleotide lacking modified nucleosides and E. coli tRNA(fMet). The all-RNA 77-nucleotide oligomer can be aminoacylated by E. coli methionyl-tRNA synthetase preparation from E. coli with methionine and threonylated in the A37 position using a yeast extract. In agreement with work by Khan and Roe using tDNA(Phe) and tDNA(Lys), the rA77-DNA(fMet) can be aminoacylated, and preliminary evidence suggests that it can be threonylated to a small extent. Kinetic data support the notion that aminoacylation of tRNA(fMet) does not depend on the presence of 2'-hydroxyl groups with the exception of that in the 3'-terminal nucleotide.
逐步的固相化学合成已提供了与大肠杆菌甲硫氨酸转运RNA(tRNA(fMet))序列相关的长RNA和DNA聚合物。已合成了与tRNA分子5'-半序列相对应的34个核糖核苷酸的寡聚物,然后通过凝胶纯化、末端核苷酸测定和序列分析对其进行了表征。该34核苷酸寡聚物在RNA连接酶催化的反应中作为受体,与对应于tRNA(fMet) 3'-半分子序列的磷酸化43核糖核苷酸寡聚物反应。具有tRNA(fMet)序列的DNA分子是一个76脱氧核糖核苷酸寡聚物,其3'-末端有一个核糖腺苷残基,所有的U残基都被T取代。这些聚合物已与一种除3'-末端2'-OH外缺少所有2'-羟基的寡脱氧核糖核苷酸、一种缺少修饰核苷的寡核糖核苷酸以及大肠杆菌tRNA(fMet)进行了比较。全RNA的77核苷酸寡聚物可以被来自大肠杆菌的甲硫氨酸-tRNA合成酶制剂用甲硫氨酸进行氨酰化,并使用酵母提取物在A37位置进行苏氨酰化。与Khan和Roe使用tDNA(Phe)和tDNA(Lys)的工作一致,rA77-DNA(fMet)可以被氨酰化,初步证据表明它可以在一定程度上被苏氨酰化。动力学数据支持这样一种观点,即tRNA(fMet)的氨酰化除了3'-末端核苷酸中的2'-羟基外,不依赖于2'-羟基的存在。