Reporter assay systems for [URE3] detection and analysis

被引:21
作者
Brachmann, Andreas
Toombs, James A.
Ross, Eric D.
机构
[1] Univ Munich, Dept Biol 1, D-80638 Munich, Germany
[2] Colorado State Univ, Dept Biochem & Mol Biol, Ft Collins, CO 80523 USA
基金
美国国家卫生研究院;
关键词
Ure2p; prion; amyloid; URE3; yeast; reporters;
D O I
10.1016/j.ymeth.2006.04.008
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The Saccharomyces cerevisiae prion [URE3] is the infectious amyloid form of the Ure2p, protein. [URE3] provides a useful model system for studying amyloid formation and stability in vivo. When grown in the presence of a good nitrogen source, [URE3] cells are able to take up ureidosuccinate, an intermediate in uracil biosynthesis, while cells lacking the [URE3] prion can not. This ability to take up ureidosuccinate has been commonly used to assay for the presence of [URE3]. However, this assay has a number of practical limitations, affecting the range of experiments that can be performed with [URE3]. Here, we describe recently developed alternative selection methods for the presence or absence of [URE3]. They make use of the Ure2p-regulated DAL5 promoter in conjunction with ADE2, URA3, kanMX, and CAN1 reporter genes, and allow for higher stringency in selection both for and against [URE3], nonselective assay of prion variants, and direct transformation of prion filaments. We discuss advantages and limitations of each of these assays. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:35 / 42
页数:8
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