Rooney R J, Harding J D
Department of Biological Sciences, Columbia University, New York, NY 10027.
Nucleic Acids Res. 1988 Mar 25;16(6):2509-21. doi: 10.1093/nar/16.6.2509.
The transcriptional properties of two cloned mouse tRNAAsp genes were examined in vitro. The tRNA(2Asp) gene displays a five fold greater transcriptional activity than the tRNA(1Asp) gene and a greater ability to form stable complexes with transcription factors. Transcription of a hybrid gene with swapped 5' flanking sequences and of 5' flanking region deletion mutants demonstrates that the differential transcription of the genes results from stimulatory sequences in the 5' flanking region of the tRNA(2Asp) gene. Distal sequences including those between positions -53 and -31 stimulate transcription but do not affect factor binding. Proximal sequences between positions -9 and -1 enhance factor binding. Thus, binding of transcription factors and later steps required for transcription can be modulated by separate and distinct 5' flanking sequence motifs in eukaryotic tRNA genes.
在体外研究了两个克隆的小鼠天冬氨酸tRNA基因的转录特性。tRNA(2Asp)基因的转录活性比tRNA(1Asp)基因高五倍,并且与转录因子形成稳定复合物的能力更强。对具有交换的5'侧翼序列的杂交基因和5'侧翼区域缺失突变体的转录表明,基因的差异转录源于tRNA(2Asp)基因5'侧翼区域中的刺激序列。包括-53至-31位之间的序列在内的远端序列刺激转录,但不影响因子结合。-9至-1位之间的近端序列增强因子结合。因此,转录因子的结合以及转录所需的后续步骤可由真核tRNA基因中单独且不同的5'侧翼序列基序调节。