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串联重复的147 bp元件导致酿酒酵母不同MAL启动子的结构和功能变异。

Tandemly repeated 147 bp elements cause structural and functional variation in divergent MAL promoters of Saccharomyces cerevisiae.

作者信息

Bell P J, Higgins V J, Dawes I W, Bissinger P H

机构信息

Burns Philp Research and Development, New South Wales, Australia.

出版信息

Yeast. 1997 Sep 30;13(12):1135-44. doi: 10.1002/(SICI)1097-0061(19970930)13:12<1135::AID-YEA162>3.0.CO;2-1.

Abstract

We have studied four novel MAL promoters isolated from a single strain of bakers' yeast. Within these promoters we have identified up to five tandem 147 bp repeats located between the MAL UAS region and the MALT TATA box. These repeats strongly reduce MALT (maltose permease) gene expression but only weakly reduce MALS (maltase) gene expression. Insertion of the 147 bp elements into the heterologous CYC1 promoter reduced expression when located between the CYC1 UAS and the TATA box, but not when located upstream of the UAS. We propose that these naturally occurring repeats have evolved as a mechanism to lower the level of MALT expression relative of MALS expression, thus avoiding possible toxic effects associated with over-expression from multiple copies of the permease gene.

摘要

我们研究了从单一面包酵母菌株中分离出的四种新型MAL启动子。在这些启动子中,我们在MAL上游激活序列(UAS)区域和MALT TATA框之间鉴定出多达五个串联的147 bp重复序列。这些重复序列强烈降低MALT(麦芽糖通透酶)基因的表达,但仅微弱降低MALS(麦芽糖酶)基因的表达。当147 bp元件插入异源CYC1启动子时,位于CYC1 UAS和TATA框之间时会降低表达,但位于UAS上游时则不会。我们提出,这些天然存在的重复序列已经进化成为一种机制,以相对于MALS表达降低MALT表达水平,从而避免与通透酶基因多个拷贝的过表达相关的可能毒性作用。

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