Wetzel R, Kohli J, Altruda F, Söll D
Mol Gen Genet. 1979 May 4;172(2):221-8. doi: 10.1007/BF00268286.
Using the translation of rabbit globin mRNA in wheat germ extracts as an assay for ochre and opal suppression, a UGA suppressor tRNA from Schizosaccharomyces pombre strain sup8-e was purified by column chromatography and two-dimensional gel electrophoresis. The purified tRNA can be aminoacylated with leucine by a crude aminoacyl-tRNA synthetase preparation from a wild type S. pombe strain, and has high activity in the suppressor assay. By a combination of post-labeling fingerprinting and rapid gel sequencing methods the nucleotide sequence of this suppressor tRNA was determined to be: pG-C-G-G-C-U-A-U-G-C-C-ac4C-G-A-G-D-G-G-D-G-D-A-A-G-G-G-m22G-G-C-A-G-A-psi-U-U*-C-A-m1G-C-C-C-U-G-C-U-G-U-U-G-U-A-A-A-A-C-G-m5C-G-A-G-A-G-T-psi-C-G-m1A-A-C-C-U-C-U-C-U-G-G-C-C-G-C-A-C-C-AOH. The anticodon sequence U*CA is complementary to the UGA codon. An interesting feature of the suppressor tRNA is an expanded anticodon loop of nine nucleotides owing to an A-C nonpair at the first anticodon stem position.
利用兔珠蛋白mRNA在小麦胚提取物中的翻译作为赭石型和乳白型抑制的检测方法,通过柱色谱和二维凝胶电泳从粟酒裂殖酵母菌株sup8-e中纯化出一种UGA抑制性tRNA。纯化后的tRNA可被来自野生型粟酒裂殖酵母菌株的粗氨酰-tRNA合成酶制剂用亮氨酸进行氨酰化,并且在抑制检测中具有高活性。通过后标记指纹图谱和快速凝胶测序方法相结合,确定了这种抑制性tRNA的核苷酸序列为:pG-C-G-G-C-U-A-U-G-C-C-ac4C-G-A-G-D-G-G-D-G-D-A-A-G-G-G-m22G-G-C-A-G-A-psi-U-U*-C-A-m1G-C-C-C-U-G-C-U-G-U-U-G-U-A-A-A-A-C-G-m5C-G-A-G-A-G-T-psi-C-G-m1A-A-C-C-U-C-U-C-U-G-G-C-C-G-C-A-C-C-AOH。反密码子序列U*CA与UGA密码子互补。这种抑制性tRNA的一个有趣特征是,由于第一个反密码子茎位置的A-C非配对,其反密码子环扩展为九个核苷酸。