Koski R A, Clarkson S G
J Biol Chem. 1982 Apr 25;257(8):4514-21.
A cloned initiator methionine tRNA gene from Xenopus laevis has been transcribed in cell-free extracts (S-100) prepared from cultured X. laevis kidney cells. RNA polymerase III produces two primary transcripts of this gene which initiate with a pppG and a pppA located seven and four nucleotides, respectively, in front of the mature tRNAMet1 5' end. Both terminate with a dT5 tract just beyond the nucleotides encoding the mature tRNA. The tRNA precursors are readily processed in vitro to mature length tRNA which contains six of the seven modified nucleotides found in the in vivo tRNAMet1. Many of these ribonucleotide modifications (m1G, m2G, m7G, D, and m1A) are introduced into the primary transcripts. The single exception is t6A which is found in the tRNAMet1 anticodon loop only after maturation of the 5' and 3' termini.
从非洲爪蟾克隆的起始甲硫氨酸tRNA基因已在由培养的非洲爪蟾肾细胞制备的无细胞提取物(S-100)中进行转录。RNA聚合酶III产生该基因的两种初级转录本,它们分别以位于成熟tRNAMet1 5'端前七个和四个核苷酸处的pppG和pppA起始。两者均在编码成熟tRNA的核苷酸之后以dT5序列终止。tRNA前体在体外很容易加工成成熟长度的tRNA,其包含体内tRNAMet1中发现的七个修饰核苷酸中的六个。许多这些核糖核苷酸修饰(m1G、m2G、m7G、D和m1A)被引入初级转录本中。唯一的例外是t6A,它仅在5'和3'末端成熟后才出现在tRNAMet1反密码子环中。