Rohan R M, Ketner G
J Biol Chem. 1983 Oct 10;258(19):11576-81.
The VA RNA genes of human adenoviruses are transcribed by RNA polymerase III and, like other RNA polymerase III transcriptional units, contain internal regulatory regions. By means of a scheme for directed mutagenesis which employs a deletion mutation to define the target, point mutations have been induced in the regulatory region of a cloned VAI gene. One mutant plasmid which fails to direct VAI transcription and several others which direct the synthesis of normal amounts of RNA of aberrant electrophoretic mobilities were identified using an in vitro transcription assay. The nucleotide sequences of the regulatory regions of three of these plasmids have been determined. All three contain mutations which fall in a block of nucleotides whose sequence (GGTTCGANNCC) is highly conserved in RNA polymerase III promoters (Galli, G., Hofstetter, H., and Birnstiel, M. L. (1981) Nature (Lond.) 294, 626-631). The VAI-negative mutant (pRR5028) contains a G leads to A transition mutation at the second position, which is invariant in functional RNA polymerase III promoters. One mobility variant carries three point mutations, including one G leads to A base change at the position adjacent on the 5' side to that altered in pRR5028. The third mutant contains a single C leads to T transition mutation, in the final position of the conserved block.
人类腺病毒的VA RNA基因由RNA聚合酶III转录,并且与其他RNA聚合酶III转录单位一样,含有内部调控区。通过一种采用缺失突变来确定靶点的定向诱变方案,已在克隆的VAI基因的调控区诱导了点突变。使用体外转录测定法鉴定出一个无法指导VAI转录的突变体质粒以及其他几个指导合成正常量的异常电泳迁移率RNA的质粒。已确定了其中三个质粒调控区的核苷酸序列。所有三个都含有落在一段核苷酸中的突变,该核苷酸序列(GGTTCGANNCC)在RNA聚合酶III启动子中高度保守(加利,G.,霍夫施泰特,H.,和伯恩施泰因,M. L.(1981年)《自然》(伦敦)294,626 - 631)。VAI阴性突变体(pRR5028)在第二个位置含有一个G到A的转换突变,这在功能性RNA聚合酶III启动子中是不变的。一个迁移率变体携带三个点突变,包括一个在5'侧与pRR5028中改变的位置相邻的位置上的G到A碱基变化。第三个突变体在保守区的最后一个位置含有一个单一的C到T转换突变。