Shimizu M
Institute of Space & Astronautical Science, Kanagawa.
J Biochem. 1995 Jan;117(1):23-6. doi: 10.1093/oxfordjournals.jbchem.a124715.
A series of C4N hairpin RNAs bearing anticodon nucleotides at the 5' ends and a discriminator base and the sequence CCA at the 3' ends was constructed by an in vitro transcription system using T7 RNA polymerase. These RNAs were aminoacylated specifically with their cognate amino acids by reaction with aminoacyl-adenylates in the presence of a dipeptide, valyl-aspartic acid, suggesting that such hairpin RNAs are able to play the role of the present-day tRNA and that valyl-aspartic acid can perform the function of the present-day aminoacyl-tRNA synthetase as a catalyst in the aminoacylation reaction. These results should provide a useful clue to elucidating the origin of the genetic code.
利用T7 RNA聚合酶的体外转录系统构建了一系列在5'端带有反密码子核苷酸、3'端带有鉴别碱基和CCA序列的C4N发夹RNA。通过在二肽缬氨酰天冬氨酸存在下与氨酰腺苷酸反应,这些RNA被其同源氨基酸特异性氨酰化,这表明此类发夹RNA能够发挥当今tRNA的作用,并且缬氨酰天冬氨酸能够作为氨酰化反应中的催化剂发挥当今氨酰tRNA合成酶的功能。这些结果应为阐明遗传密码的起源提供有用线索。