Exploring redundancy in the yeast genome:: an improved strategy for use of the cre-loxP system

被引:105
作者
Delneri, D
Tomlin, GC
Wixon, JL
Hutter, A
Sefton, M
Louis, EJ
Oliver, SG
机构
[1] Univ Manchester, Sch Biol Sci, Manchester M13 9PT, Lancs, England
[2] UMIST, Dept Biomol Sci, Manchester M60 1QD, Lancs, England
[3] Univ Oxford, Dept Biochem, Oxford OX1 3QU, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
counter-selectable markers; cycloheximide resistance gene; gene families; multiple deletions;
D O I
10.1016/S0378-1119(00)00217-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Gene families having more than three members are a common phenomenon in the Saccharomyces cerevisiae genome. As yeast research enters the post-genome era, the development of existing deletion strategies is crucial for tackling this apparent redundancy, hence a method for performing rapid multiple gene disruptions in this organism has been developed. We constructed three replacement cassettes in which different selectable markers were placed between two loxP loci. Multiple deletions (of members of a gene family) were generated, in one strain, using sequential integration of different replacement markers (kanMX, LYS2, KlURA3 and SpHIS5). Their excision from the genome was performed simultaneously, as the final step, using a new cre recombinase vector, which carries the cycloheximide-resistance gene from Candida maltosa as a selectable marker. Our multiple gene deletion system significantly accelerates and facilitates the functional analysis process and is particularly useful for studying gene families in either laboratory or industrial yeast strains. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:127 / 135
页数:9
相关论文
共 35 条
[1]   A METHOD FOR GENE DISRUPTION THAT ALLOWS REPEATED USE OF URA3 SELECTION IN THE CONSTRUCTION OF MULTIPLY DISRUPTED YEAST STRAINS [J].
ALANI, E ;
CAO, L ;
KLECKNER, N .
GENETICS, 1987, 116 (04) :541-545
[2]   An overview of membrane transport proteins in Saccharomyces cerevisiae [J].
Andre, B .
YEAST, 1995, 11 (16) :1575-1611
[3]  
[Anonymous], 1994, METHODS YEAST GENETI
[4]  
Baganz F, 1997, YEAST, V13, P1563, DOI 10.1002/(SICI)1097-0061(199712)13:16<1563::AID-YEA240>3.0.CO
[5]  
2-6
[6]   A SIMPLE AND EFFICIENT METHOD FOR DIRECT GENE DELETION IN SACCHAROMYCES-CEREVISIAE [J].
BAUDIN, A ;
OZIERKALOGEROPOULOS, O ;
DENOUEL, A ;
LACROUTE, F ;
CULLIN, C .
NUCLEIC ACIDS RESEARCH, 1993, 21 (14) :3329-3330
[7]  
CHATTOO BB, 1979, GENETICS, V93, P51
[8]  
Delneri D, 1999, YEAST, V15, P1681, DOI 10.1002/(SICI)1097-0061(199911)15:15<1681::AID-YEA486>3.0.CO
[9]  
2-A
[10]  
Delneri D, 1999, GENETICS, V153, P1591