Venegas A, Quiroga M, Zaldivar J, Rutter W J, Valenzuela P
J Biol Chem. 1979 Dec 25;254(24):12306-9.
A library of cloned yeast DNA fragments generated by digestion of yeast DNA with the restriction endonuclease Bam HI has been screened by colony hybridization to total yeast [32P]tRNA. Four hundred colonies carrying yeast tRNA genes were isolated. By hybridization to 125I-tRNALeu3, we have isolated from this collection 14 colonies carrying fragments containing yeast tRNALeu genes. The size of the yeast Bam HI inserts ranged from 2.45 x 10(6) to 14 x 10(6) daltons. One of these fragments was mapped in detail by restriction endonuclease digestion and hybridization to 125I-tRNALeu3. The presence of a tRNALeu3 gene was confirmed by DNA sequence. The results indicate that the tRNALeu3 coding region is not co-linear with the tRNALeu3. An intervening tract of 33 base pairs interrupts the coding sequences 1 base pair past the anticodon coding region. The putative structure of a tRNALeu3 precursor is deduced in which the anticodon base pairs with residues from the intervening sequence.
用限制性内切酶Bam HI消化酵母DNA产生的克隆酵母DNA片段文库,通过与总酵母[32P]tRNA进行菌落杂交筛选。分离出了400个携带酵母tRNA基因的菌落。通过与125I-tRNALeu3杂交,我们从该文库中分离出了14个携带含有酵母tRNALeu基因片段的菌落。酵母Bam HI插入片段的大小范围为2.45×10(6)至14×10(6)道尔顿。其中一个片段通过限制性内切酶消化和与125I-tRNALeu3杂交进行了详细定位。通过DNA序列证实了tRNALeu3基因的存在。结果表明,tRNALeu3编码区与tRNALeu3不共线。一段33个碱基对的间隔序列在反密码子编码区之后1个碱基对处中断编码序列。推导了tRNALeu3前体的假定结构,其中反密码子与间隔序列的残基形成碱基对。