Yoshimura M, Inokuchi H, Ozeki H
J Mol Biol. 1984 Aug 25;177(4):627-44. doi: 10.1016/0022-2836(84)90041-x.
An Escherichia coli DNA fragment containing an Su+6 amber suppressor gene (supP) was cloned into a lambda gt lambda Ch vector by the shotgun method, selecting a Su+6 transducing phage lambda pSu+6. Through prophage integration followed by induction occurring at the transducing region of the lambda pSu+6 in Su- E. coli, a counterpart transducing phage carrying the wild-type allele (Su degrees 6) was isolated (lambda pSu degrees 6). The fingerprint of a tRNA encoded by lambda pSu degrees 6 was identical to that of an unidentified tRNAE previously reported (Ikemura & Ozeki, 1977). The cloverleaf structure of this tRNA was determined by combining the results of tRNA analysis and DNA sequencing of the gene. Judging from the anticodon of 5'-CAA-3', Su degrees 6 tRNA was identified as a new type of leucine isoacceptor in E. coli. Unlike other suppressors analyzed, Su+6 tRNA differed by two nucleotides from Su degrees 6 tRNA; one at the anticodon (CAA to CUA) and the other at the junction of D- and anticodon-stem (A27 to G27). DNA sequence analysis revealed that a single stretch of tRNA is flanked by the putative sequences of promoter and terminator. Thus a single copy of the Su degrees 6 tRNA gene constitutes a solitary tRNA transcription unit. Southern blotting showed only one copy of Su degrees 6 tRNA gene per haploid genome of E. coli. Since this single gene can mutate to the Su+6 suppressor, the Su degrees 6 leucine tRNA may be accounted as a dispensable species among the leucine isoacceptor tRNAs. Two possible open reading frames are found immediately following the Su degrees 6 tRNA gene.
通过鸟枪法将含有琥珀抑制基因(supP)的大肠杆菌DNA片段克隆到λgtλCh载体中,筛选出一个携带Su +6的转导噬菌体λpSu +6。通过原噬菌体整合,随后在Su -大肠杆菌中λpSu +6的转导区域发生诱导,分离出携带野生型等位基因(Su°6)的对应转导噬菌体(λpSu°6)。λpSu°6编码的一种tRNA的指纹图谱与先前报道的一种未鉴定的tRNAE相同(池村和小関,1977)。通过结合tRNA分析结果和该基因的DNA测序确定了这种tRNA的三叶草结构。从5'-CAA-3'的反密码子判断,Su°6 tRNA被鉴定为大肠杆菌中一种新型的亮氨酸同功受体。与其他分析的抑制子不同,Su +6 tRNA与Su°6 tRNA在两个核苷酸上存在差异;一个在反密码子处(CAA变为CUA),另一个在D环和反密码子茎的连接处(A27变为G27)。DNA序列分析表明,一段单一的tRNA侧翼是启动子和终止子的假定序列。因此,Su°6 tRNA基因的单拷贝构成了一个单独的tRNA转录单元。Southern杂交显示,大肠杆菌单倍体基因组中每个基因组只有一份Su°6 tRNA基因拷贝。由于这个单一基因可以突变为Su +6抑制子,Su°6亮氨酸tRNA可能被视为亮氨酸同功受体tRNA中的一种可有可无的类型。在Su°6 tRNA基因之后立即发现了两个可能的开放阅读框。