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Organization of multiple regulatory elements in the control region of the adenovirus type 2-specific VARNA1 gene: fine mapping with linker-scanning mutants.

机译:腺病毒2型特异性VARNA1基因控制区域中多个调控元件的组织:与接头扫描突变体的精细定位。

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摘要

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.
机译:腺病毒2型特异性病毒相关RNA 1(VARNA1)基因通过真核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基因具有较大的控制区域,该区域由几个调控元件组成。在该基因的控制区域中从-33到+77的25个精确的接头扫描突变被用于定义这些元素的数量和边界。这些突变对人类KB细胞提取物中的转录和转录因子竞争的影响揭示了五个积极的调控因素。转录和形成稳定复合物绝对需要与B嵌段相符的必需元素。转录和稳定复合物的形成也需要第二个元素,包括A嵌段。尽管此元素不像B块元素那么重要,但与B块元素一起,对于形成最基本形式的转录机制可能是必需的。因此,这两个元件是该基因中的启动子元件。另外,有效转录也需要在嵌段间区域中的一个可能的元件和在5'侧翼区域中的两个元件,但是对于形成稳定的复合物则适度地需要它们。正如预期的那样,使用293细胞提取物刺激这些突变体和野生型基因的转录至少是用KB细胞提取物刺激的三倍。但是,当将293细胞提取物用于这些突变体的转录时,发现了该基因的类似调控元件,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。

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