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用于基因功能系统分析的新型酵母载体家族及源自S288C的菌株

A new family of yeast vectors and S288C-derived strains for the systematic analysis of gene function.

作者信息

Tomlin G C, Wixon J L, Bolotin-Fukuhara M, Oliver S G

机构信息

School of Biological Sciences, 2.205 Stopford Building, University of Manchester, Oxford Road, Manchester M13 9PT, UK.

出版信息

Yeast. 2001 Apr;18(6):563-75. doi: 10.1002/yea.703.

Abstract

The yeast genome has been shown to contain a significant number of gene families with more than three members. In order to study these families it is often necessary to generate strains carrying deletions of all members of the family, which can require a wide range of auxotrophic markers. To facilitate such studies, we have generated yeast strains containing deletions of a selection of nutritional marker genes (ade2, ade4, ade8, met3 and met14). We have also cloned the corresponding cognate genes, allowing their use in PCR-based gene disruptions. Two new pRS family Saccharomyces cerevisiae-Escherichia coli shuttle vectors containing ADE8 (one low-copy, pRS4110, and one high-copy, pRS4210) have been produced for use in conjunction with the new strains. A system for easier synthetic lethal screening using one of these new markers is also presented. The ADE8 and HIS3 genes have been cloned together on a high-copy vector (pRS4213), providing a plasmid for red-white colour screening in the ade2 Delta 0 ade8 Delta 0 strains we have generated. In contrast to some conventional systems, this plasmid allows for screening using gene libraries constructed in URA3 plasmids.

摘要

酵母基因组已被证明含有大量成员超过三个的基因家族。为了研究这些家族,通常需要构建携带该家族所有成员缺失的菌株,这可能需要多种营养缺陷型标记。为便于此类研究,我们构建了一系列酵母菌株,这些菌株缺失了部分营养标记基因(ade2、ade4、ade8、met3和met14)。我们还克隆了相应的同源基因,以便用于基于PCR的基因敲除。我们构建了两个新的pRS家族酿酒酵母-大肠杆菌穿梭载体,其中包含ADE8基因(一个低拷贝载体pRS4110和一个高拷贝载体pRS4210),用于与新构建的菌株配合使用。我们还提出了一种利用这些新标记之一进行更简便的合成致死筛选的系统。ADE8和HIS3基因已被克隆到一个高拷贝载体(pRS4213)上,为我们构建的ade2Δ0 ade8Δ0菌株提供了一种用于红白颜色筛选的质粒。与一些传统系统不同,该质粒允许使用在URA3质粒中构建的基因文库进行筛选。

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