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使用RNA聚合酶III启动子的酵母表达载体。

Yeast expression vectors using RNA polymerase III promoters.

作者信息

Good P D, Engelke D R

机构信息

Department of Biological Chemistry, University of Michigan, Ann Arbor 48109-0606.

出版信息

Gene. 1994 Dec 30;151(1-2):209-14. doi: 10.1016/0378-1119(94)90658-0.

Abstract

A series of Saccharomyces cerevisiae--Escherichia coli shuttle vectors is described in which small RNAs can be stably expressed in yeast from two different promoters for RNA polymerase III transcription. The vectors are available in either high- or low-copy-number forms with either URA3, HIS3, or TRP1 selection markers, and are based on a previously described set of plasmid vectors [Sikorski and Hieter, Genetics 122 (1989) 19-27]. Transcripts have structured pre-tRNA or RPR1 leaders fused to RNA corresponding to inserted sequences. Levels of RNA accumulation are dependent on plasmid copy number and the type of transcript.

摘要

本文描述了一系列酿酒酵母-大肠杆菌穿梭载体,其中小RNA可在酵母中从两个不同的RNA聚合酶III转录启动子稳定表达。这些载体有高拷贝数或低拷贝数形式,带有URA3、HIS3或TRP1选择标记,并且基于先前描述的一组质粒载体[Sikorski和Hieter,遗传学122(1989)19-27]。转录本具有与插入序列对应的RNA融合的结构化前体tRNA或RPR1前导序列。RNA积累水平取决于质粒拷贝数和转录本类型。

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