Robinson R R, Davidson N
Cell. 1981 Jan;23(1):251-9. doi: 10.1016/0092-8674(81)90289-0.
A recombinant DNA phage containing a cluster of Drosophila melanogaster tRNA genes has been isolated and analyzed. The insert of this phage has been mapped by in situ hybridization to chromosomal region 50AB, a known tRNA site. Nucleotide sequencing of the entire Drosophila tRNA coding region reveals seven tRNA genes spanning 2.5 kb of chromosomal DNA. This cluster is separated from other tRNA regions on the chromosome by at least 2.7 kb on one side, and 9.6 kb on the other. Two tRNA genes are nearly identical and contain intervening sequences of length 38 and 45 bases, respectively, in the anticodon loop. These two genes are assigned to be tRNALeu genes because of significant sequence homology with yeast tRNA3Leu, and secondary structure homology with yeast tRNA3Leu intervening sequence. In addition, an 8 base sequence (AAAAUCUU) is conserved in the same location in the intervening sequences of Drosophila tRNALeu genes and a yeast tRNA3Leu gene. Similar sequenes occur in all other tRNAs containing intervening sequences. The remaining five genes are identical tRNAIle genes, which are also identical to a tRNAIle gene from chromosomal region 42A. The 5' flanking regions are only weakly homologous, but each set of isoacceptors contains short regions of strong homology approximately 20 nucleotides preceding the tRNA coding sequences: GCNTTTTG preceding tRNAIle genes; and GANTTTGG preceding tRNALeu genes. The genes are irregularly distributed on both DNA strands; spacing regions are divergent in sequence and length.
一个含有果蝇tRNA基因簇的重组DNA噬菌体已被分离和分析。该噬菌体的插入片段已通过原位杂交定位到染色体区域50AB,这是一个已知的tRNA位点。对整个果蝇tRNA编码区的核苷酸测序揭示了七个tRNA基因,跨越2.5kb的染色体DNA。这个基因簇与染色体上的其他tRNA区域在一侧至少相隔2.7kb,在另一侧相隔9.6kb。两个tRNA基因几乎相同,在反密码子环中分别含有长度为38和45个碱基的间隔序列。由于与酵母tRNA3Leu有显著的序列同源性,以及与酵母tRNA3Leu间隔序列有二级结构同源性,这两个基因被确定为tRNALeu基因。此外,一个8碱基序列(AAAAUCUU)在果蝇tRNALeu基因和一个酵母tRNA3Leu基因的间隔序列的相同位置保守。在所有其他含有间隔序列的tRNA中也出现类似序列。其余五个基因是相同的tRNAIle基因,它们也与来自染色体区域42A的一个tRNAIle基因相同。5'侧翼区域只有微弱的同源性,但每组同功受体在tRNA编码序列之前大约20个核苷酸处都含有短的强同源区域:tRNAIle基因之前是GCNTTTTG;tRNALeu基因之前是GANTTTGG。这些基因在两条DNA链上分布不规则;间隔区域在序列和长度上是不同的。