Trivedi A, Young L S, Ouyang C, Johnson D L, Sprague K U
Departments of Molecular Pharmacology and Biochemistry, Schools of Pharmacy and Medicine, University of Southern California, Los Angeles, California 90033, USA.
J Biol Chem. 1999 Apr 16;274(16):11369-75. doi: 10.1074/jbc.274.16.11369.
In contrast to yeast and mammalian systems, which depend principally on internal promoter elements for tRNA gene transcription, insect systems require additional upstream sequences. To understand the function of the upstream sequences, we have asked whether the Bombyx mori tRNACAla and tRNASGAla genes, which are absolutely dependent on these sequences in vitro, also require them for transcription in vivo. We introduced wild-type and mutant versions of the Bombyx tRNAAla genes into Drosophila Schneider-2 cells and found that the tRNACAla gene is efficiently transcribed and that its transcription depends strongly on the distal segment of its upstream promoter. In contrast, the tRNASGAla gene is inefficiently transcribed, and this inefficiency results from lack of a specific sequence within the distal tRNACAla upstream promoter. This sequence, 5'-TTTATAT-3', is sufficient to increase the activity of the tRNASGAla promoter to that of the tRNACAla promoter. Moreover, promoters containing the 5'-TTTATAT-3' element are stimulated by increased levels of cellular TATA-binding protein. Together these results indicate that, in insect cells, a TATA-like element is specifically required to form functional TATA-binding protein-containing complexes that promote efficient transcription of tRNA genes.
与主要依赖内部启动子元件进行tRNA基因转录的酵母和哺乳动物系统不同,昆虫系统需要额外的上游序列。为了了解上游序列的功能,我们研究了家蚕tRNACAla和tRNASGAla基因,它们在体外绝对依赖于这些序列,在体内转录时是否也需要它们。我们将家蚕tRNAAla基因的野生型和突变型导入果蝇Schneider-2细胞,发现tRNACAla基因能高效转录,其转录强烈依赖于上游启动子的远端片段。相比之下,tRNASGAla基因转录效率低下,这种低效率是由于tRNACAla上游启动子远端缺乏特定序列所致。该序列5'-TTTATAT-3'足以将tRNASGAla启动子的活性提高到tRNACAla启动子的水平。此外,含有5'-TTTATAT-3'元件的启动子受到细胞TATA结合蛋白水平升高的刺激。这些结果共同表明,在昆虫细胞中,特异性需要一个类似TATA的元件来形成促进tRNA基因高效转录的含功能性TATA结合蛋白的复合物。