Roy K L, Cooke H, Buckland R
Nucleic Acids Res. 1982 Nov 25;10(22):7313-22. doi: 10.1093/nar/10.22.7313.
A 1.65 kb segment of DNA from a human-lambda recombinant, selected for human tRNA genes, was subcloned in the plasmid pAT 153 for sequence determination. Three human tRNA genes were found; one, a tRNAlys gene which appears to specify a tRNA identical in sequence to the previously described tRNA3lys from rat liver (AAA,G); another a tRNAgln gene, the product of which would be expected to recognize only the codon CAG; and a third which would direct synthesis of a tRNAleu specific for CUA and G. Intervening sequences are not found in any of these genes. The three tRNA genes are separated by about 0.5 kb segments of DNA containing no apparent informational sequences. Examination of flanking sequences shows some similarities at the 5'-ends of the three genes, but less similarity to 5' flanking sequences of tRNA genes in other eucaryotes. All three tRNA genes direct synthesis of appropriate sized products in a HeLa cell lysate in vitro transcription system.
从一个经人λ重组体筛选出的含有人tRNA基因的1.65 kb DNA片段,被亚克隆到质粒pAT 153中用于序列测定。发现了三个人类tRNA基因;一个是tRNAlys基因,其编码的tRNA序列似乎与先前描述的大鼠肝脏tRNA3lys(AAA,G)相同;另一个是tRNAgln基因,预期其产物仅识别密码子CAG;第三个基因指导合成对CUA和G特异的tRNAleu。在这些基因中均未发现间隔序列。这三个tRNA基因被约0.5 kb不含明显信息序列的DNA片段隔开。对侧翼序列的检查显示,这三个基因的5'端有一些相似性,但与其他真核生物中tRNA基因的5'侧翼序列的相似性较低。在HeLa细胞裂解物体外转录系统中,所有这三个tRNA基因都指导合成了大小合适的产物。