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Conserved sequence elements upstream of the gene encoding yeast ribosomal protein L25 are involved in transcription activation.

机译:编码酵母核糖体蛋白L25的基因上游的保守序列元件参与转录激活。

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摘要

Previous studies have revealed the occurrence of two closely linked conserved sequence elements, designated as HOMOL 1 and RPG box, in front of most yeast ribosomal protein genes examined. To investigate whether these conserved nucleotide elements play a role in the regulation of ribosomal protein gene expression, we performed deletion analysis of the DNA region upstream of the gene encoding ribosomal protein L25. To that end we constructed a hybrid gene consisting of the pertinent 5'-flanking sequence and the Escherichia coli galK marker gene. The effects on the transcription of this fusion gene of Bal31-generated deletions were measured by Northern analysis of RNA isolated from the respective transformed yeast cells. The results demonstrate that removal of one box has a detrimental effect on the level of transcription, whereas after the deletion of both boxes hardly any transcription can be observed. Subsequently we inserted synthetic oligonucleotides in the upstream region of an L25 gene from which the original boxes had been removed. Expression of the inactivated hybrid gene turned out to be restored even by insertion of one RPG element. Moreover, the RPG box functions in both orientations, though not with equal efficiency.
机译:先前的研究表明,在检查的大多数酵母核糖体蛋白基因之前,存在着两个紧密相连的保守序列元件,分别称为HOMOL 1和RPG box。为了研究这些保守的核苷酸元件是否在核糖体蛋白基因表达的调节中起作用,我们对编码核糖体蛋白L25的基因上游的DNA区域进行了缺失分析。为此,我们构建了由相关的5'侧翼序列和大肠杆菌galK标记基因组成的杂种基因。 Bal31产生的缺失对该融合基因的转录的影响通过对从各自转化的酵母细胞中分离的RNA的RNA进行Northern分析来测量。结果表明,删除一个框对转录水平有不利影响,而删除两个框后,几乎看不到任何转录。随后,我们将合成的寡核苷酸插入已去除原始框的L25基因的上游区域。甚至通过插入一个RPG元件也证明了失活的杂交基因的表达得以恢复。而且,RPG盒在两个方向上都可以起作用,尽管效率不尽相同。

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