Schaack J, Sharp S, Dingermann T, Burke D J, Cooley L, Söll D
J Biol Chem. 1984 Feb 10;259(3):1461-7.
We have examined the 5'-and 3'-flanking sequence requirements for the "wild type transcription properties" of a Drosophila tRNA Arg gene through the use of transcription assays in cell-free extracts. Thirty-three base pairs of the 5' flank immediately adjacent to the sequence encoding the mature tRNA are necessary for efficient transcription in Drosophila Kc cell extract. Sequences affecting factor binding to form stable transcription complexes extend more than 60 base pairs into the 5' flank, and approximately 35 base pairs into the 3' flank. HeLa cell extract exhibits dependence, albeit reduced, on the same 5'-flanking sequence; it also has 3'-flanking sequence requirements for maximal stable complex formation. This requirement of in vitro transcription for flanking sequence is not dependent on the use of a homologous system, but is dependent on the cellular source of the extract.
我们通过在无细胞提取物中进行转录分析,研究了果蝇tRNA Arg基因“野生型转录特性”对5'和3'侧翼序列的要求。与编码成熟tRNA的序列紧邻的5'侧翼的33个碱基对,对于在果蝇Kc细胞提取物中的高效转录是必需的。影响因子结合以形成稳定转录复合物的序列在5'侧翼延伸超过60个碱基对,在3'侧翼延伸约35个碱基对。HeLa细胞提取物对相同的5'侧翼序列也有依赖性,尽管有所降低;它对最大程度稳定复合物形成也有3'侧翼序列要求。体外转录对侧翼序列的这种要求不依赖于同源系统的使用,而是依赖于提取物的细胞来源。