Railey J F, Wu G J
Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia 30322.
Mol Cell Biol. 1988 Mar;8(3):1147-59. doi: 10.1128/mcb.8.3.1147-1159.1988.
The adenovirus type 2-specific virus-associated RNA 1 (VARNA1) gene is transcribed by eucaryotic RNA polymerase III. Previous studies using deletion mutants for transcription have shown that the VARNA1 gene has a large control region which is composed of several regulatory elements. Twenty-five exact linker-scanning mutations in the control region, from -33 to +77, of this gene were used for definition of the number and boundaries of these elements. The effects of these mutations on transcription and competition for transcription factors in human KB cell extracts revealed five positive regulatory elements. The essential element, which coincided with the B block, was absolutely required for both transcription and formation of stable complexes. A second element, which included the A block, was also required for both transcription and formation of stable complexes. Although this element is not as essential as the B-block element, together with the B-block element it may be necessary for formation of the most basal form of transcription machinery. Therefore, these two elements are the promoter elements in this gene. In addition, one possible element in the interblock region and two elements in the 5' flanking region were also required for efficient transcription, but they were moderately required for formation of stable complexes. Transcription of these mutants and the wild-type gene using an extract of 293 cells was stimulated at least threefold over that with the KB cell extract, as expected. Similar regulatory elements of this gene were revealed, however, when the 293 cell extract was used for transcription of these mutants, suggesting that the E1A-mediated specific transcription factors act on the transcription machinery in a sequence-nonspecific manner.
2型腺病毒特异性病毒相关RNA 1(VARNA1)基因由真核RNA聚合酶III转录。先前使用缺失突变体进行转录的研究表明,VARNA1基因有一个由几个调控元件组成的大控制区。该基因控制区(从-33到+77)中的25个精确的接头扫描突变用于确定这些元件的数量和边界。这些突变对人KB细胞提取物中转录及转录因子竞争的影响揭示了五个正调控元件。与B区一致的必需元件对于转录和稳定复合物的形成都是绝对必需的。第二个元件包括A区,对于转录和稳定复合物的形成也同样必需。尽管该元件不像B区元件那样必需,但与B区元件一起,它可能是形成最基本形式的转录机制所必需的。因此,这两个元件是该基因中的启动子元件。此外,有效转录还需要间隔区中的一个可能元件和5'侧翼区中的两个元件,但它们对于稳定复合物的形成只是适度必需的。正如预期的那样,使用293细胞提取物对这些突变体和野生型基因进行转录,其刺激程度比使用KB细胞提取物至少高三倍。然而,当使用293细胞提取物对这些突变体进行转录时,也揭示了该基因类似的调控元件,这表明E1A介导的特异性转录因子以序列非特异性的方式作用于转录机制。