Ghosh K, Ghosh H P
Nucleic Acids Res. 1984 Jun 25;12(12):4997-5003. doi: 10.1093/nar/12.12.4997.
The coding properties of tRNATrp from yeast and wheat germ were studied. Unlike E. coli tRNATrp or mitochondrial tRNATrp, eukaryotic tRNATrp did not recognize the UGA codon in vitro. The sequence of wheat germ tRNATrp as determined by [32P] post-labelling techniques is: [sequence in text] The interesting features are: (i) Presence of a C11:G24 base pair in contrast to the U11:G24 in E. coli Su- tRNATrp. (ii) The anticodon sequence is -CmCA- compared to -CCA- in E. coli tRNATrp. (iii) Lack of a hypermodified base i6A adjacent to the 3'-end of the anticodon. (iv) Presence of -T psi CG- sequence instead of -psi psi CG- sequence present in mammalian tRNATrp.
对来自酵母和小麦胚芽的色氨酸转运RNA(tRNATrp)的编码特性进行了研究。与大肠杆菌tRNATrp或线粒体tRNATrp不同,真核生物tRNATrp在体外不识别UGA密码子。通过[32P]后标记技术确定的小麦胚芽tRNATrp序列为:[文本中的序列]。有趣的特征有:(i)存在C11:G24碱基对,而大肠杆菌琥珀抑制tRNATrp中为U11:G24。(ii)反密码子序列为-CmCA-,而大肠杆菌tRNATrp中为-CCA-。(iii)在反密码子3'端相邻处缺乏超修饰碱基i6A。(iv)存在-TψCG-序列,而非哺乳动物tRNATrp中存在的-ψψCG-序列。