Hauber J, Nelböck P, Pilz U, Feldmann H
Biol Chem Hoppe Seyler. 1986 Nov;367(11):1141-6. doi: 10.1515/bchm3.1986.367.2.1141.
In the yeast Saccharomyces cerevisiae, the majority of the tRNA genes are found associated with transposable elements one of which is the Ty element. We noticed that the transcriptional activity of several of these genes was rather different depending on the type of the accompanying element(s) [Nelböck et al. (1985) Biol. Chem. Hoppe-Seyler 366, 1041-1051]. In order to study the influence of a Ty element on tRNA gene expression, we used the method of micro-injection into Xenopus oocytes taking advantage of a Ty+/Ty- allelic pair of a tRNALys1 gene recently isolated in our laboratory. A direct comparison showed that the expression of the plus allele was c. sixfold higher than that of the minus allele. In order to determine sequences of the Ty responsible for this effect, we constructed a number of variants in which distinct segments of the Ty were deleted or rearranged. The activating ability was localized to a 590-bp segment of the Ty containing the 'promoter delta', independent of its orientation or location towards the tRNA gene thus resembling the effects described for transcriptional enhancers. This is the first time that a long-range effect has been observed on the expression of a gene transcribed by RNA polymerase III.
在酿酒酵母中,大多数tRNA基因与转座元件相关联,其中之一是Ty元件。我们注意到,这些基因中的几个基因的转录活性因伴随元件的类型而异[内尔博克等人(1985年),《生物化学,霍佩 - 赛勒》366卷,第1041 - 1051页]。为了研究Ty元件对tRNA基因表达的影响,我们利用最近在我们实验室分离的tRNALys1基因的Ty + / Ty - 等位基因对,采用显微注射到非洲爪蟾卵母细胞中的方法。直接比较表明,正等位基因的表达比负等位基因高约六倍。为了确定Ty中负责这种效应的序列,我们构建了许多变体,其中Ty的不同片段被删除或重排。激活能力定位于Ty的一个590 bp片段,该片段包含“启动子δ”,与其相对于tRNA基因的方向或位置无关,因此类似于对转录增强子所描述的效应。这是首次观察到对由RNA聚合酶III转录的基因表达的远距离效应。