Guthrie C, McClain W H
Biochemistry. 1979 Aug 21;18(17):3786-95. doi: 10.1021/bi00584a023.
One of the eight tRNA species coded by bacteriophage T4 is unique in that (1) it is found in a yield lower by three- to fourfold than that of any other tRNA and (2) while dispensable for growth in standard laboratory hosts, it is essential for phage propagation in a natural isolate of Escherichia coli (strain CT439). We report here the nucleotide sequence of this tRNA and of several mutationally altered forms. The molecule is 77 nucleotides in length and has the anticodon N-A-U. Depending on the pairing properties of the "wobble" nucleotide N, this sequence could correspond to one or more of the isoleucine-specific codons (formula: see text) or to the methionine-specific codon A-U-G. Since a T4-specific acceptor activity for isoleucine which is stimulated in ribosome binding by A-U-A but not A-U-U has been reported previously, we infer that we have sequenced a tRNA Ile species which preferentially recognizes A-U-A. Mutant HA1 is unable to grow in CT439; it produces no tRNA Ile. The primary mutational alteration is a transition four residues from the 5'terminus which converts a C.G to a U.G base pair. The consequences of this lesion can be partially reversed by second-site mutations nearby in the acceptor stem. Unexpectedly, the tRNA Ile synthesized in these revertants still retains two unusual structural features found in the wild-type molecule: the opposition of two Up residues in the amino acid acceptor stem and the opposition of an Ap and a Gp residue in the anticodon stem. Implications of these structual anomalies for a possibly unique physiological role of this minor tRNA species are discussed.
由噬菌体T4编码的八种tRNA种类之一具有独特之处,即:(1)它的产量比其他任何tRNA低三到四倍;(2)虽然在标准实验室宿主中生长时它是可有可无的,但对于噬菌体在大肠杆菌的自然分离株(CT439菌株)中的繁殖却是必不可少的。我们在此报告这种tRNA及其几种突变形式的核苷酸序列。该分子长度为77个核苷酸,反密码子为N-A-U。根据“摆动”核苷酸N的配对特性,该序列可能对应于一个或多个异亮氨酸特异性密码子(公式:见正文)或甲硫氨酸特异性密码子A-U-G。由于先前已报道了一种T4特异性异亮氨酸受体活性,其在核糖体结合中被A-U-A而非A-U-U刺激,我们推断我们已对优先识别A-U-A的异亮氨酸tRNA种类进行了测序。突变体HA1在CT439中无法生长;它不产生异亮氨酸tRNA。主要的突变改变是在5'末端起四个残基处的一个转换,将一个C.G碱基对转换为U.G碱基对。该损伤的后果可被受体茎附近的第二位点突变部分逆转。出乎意料的是,在这些回复突变体中合成的异亮氨酸tRNA仍然保留了野生型分子中发现的两个不寻常的结构特征:氨基酸受体茎中两个Up残基的相对以及反密码子茎中一个Ap和一个Gp残基的相对。讨论了这些结构异常对于这种次要tRNA种类可能独特的生理作用的影响。