REPLICATION IN SACCHAROMYCES-CEREVISIAE OF PLASMID PBR313 CARRYING DNA FROM THE YEAST TRPL REGION

被引:124
作者
KINGSMAN, AJ
CLARKE, L
MORTIMER, RK
CARBON, J
机构
[1] Department of Biological Sciences, University of California, Santa Barbara
关键词
E. coli-yeast recombinant DNA; Southern hybridization; spheroplast fusion; Transformation; yeast cloning vector;
D O I
10.1016/0378-1119(79)90029-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Plasmid pBR313 carrying a 1.4 kb EcoRI fragment from the yeast TRP1 region (designated pLC544) is capable of transforming yeast trp1 mutants to Trp+ at high frequency (103-104 transformants/μg DNA). Transformation can be achieved either by using purified plasmid DNA or by fusion of yeast shperoplasts with partially lysed Escherihia coli [pLC544] photoplast preparations. The Trp+ yeast transformants are highly unstable, segregating Trp- cells at frequencies of 0.18 percell per generation (haploids) and 0.056 per cell per generation (diploids) in media containing tryptophan. Plasmid pLC544 replicates autonomously in the nucleus of yeast cells and segregation of Trp- cells is associated with the complete loss of plasmid sequences. In genetic crosses, pLC544 is randomly assorted during meiosis and is carried unchanged through the mating process into haploid recombinants. © 1979.
引用
收藏
页码:141 / 152
页数:12
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