DeFranco D, Sharp S, Söll D
J Biol Chem. 1981 Dec 10;256(23):12424-9.
Transcription of Drosophila tRNA genes is controlled by signals within and outside the region coding for the mature tRNA. Deletion analysis has revealed an oligonucleotide sequence in the 5'-flanking region of a Drosophila tRNA2Lys gene to be responsible for the poor transcriptional activity of this and of other tRNA genes. The low template activity of this gene was maintained even after deletion of the 5'-flanking region up to nucleotide -23. Removal of nine additional nucleotides resulted in complete loss of transcriptional repression. The oligonucleotide responsible for transcriptional repression is GGCAGTTTTTG and is located 13 nucleotides upstream from the mature tRNA coding sequence. Since the sequence of the undecanucleotide is well conserved within the 5'-flanking region of all known Drosophila tRNA2Lys genes, we have investigated why the transcription of all these genes is not similarly repressed. Deletion or insertion of nucleotides between the mature tRNA coding region and this oligonucleotide resulted in tRNA genes with increased template activity. This observation suggests that the position of this oligonucleotide relative to some element downstream influences the extent of transcriptional repression.
果蝇tRNA基因的转录受成熟tRNA编码区域内外信号的控制。缺失分析揭示,果蝇tRNA2Lys基因5'侧翼区域的一个寡核苷酸序列导致该基因以及其他tRNA基因转录活性低下。即使删除5'侧翼区域直至核苷酸-23,该基因的低模板活性仍得以维持。再去除另外9个核苷酸会导致转录抑制完全丧失。负责转录抑制的寡核苷酸是GGCAGTTTTTG,位于成熟tRNA编码序列上游13个核苷酸处。由于该十一核苷酸序列在所有已知果蝇tRNA2Lys基因的5'侧翼区域内高度保守,我们研究了为何所有这些基因的转录没有受到类似的抑制。在成熟tRNA编码区域与该寡核苷酸之间缺失或插入核苷酸会导致tRNA基因的模板活性增加。这一观察结果表明,该寡核苷酸相对于下游某些元件的位置会影响转录抑制的程度。