Literature DB >> 10028180

A positive selection for plasmid loss in Saccharomyces cerevisiae using galactose-inducible growth inhibitory sequences.

M Kawahata1, S Amari, Y Nishizawa, R Akada.   

Abstract

Counter-selections for the loss of introduced plasmid sequences are useful for gene manipulations in yeast. We have used GAL10 promoter-mediated overexpression of GIN sequences, which inhibit the growth of cells, to develop a novel counter-selection system. Yeast cells carrying a GIN sequence grow normally on glucose medium but are unable to grow on galactose medium, whereas derivatives that have lost the GIN sequence are able to grow in the presence of galactose. We constructed autonomously replicating, integrating, and disruption plasmids carrying GIN sequences and tested their use to select for loss of the plasmid. The results showed that the GIN sequences provide a selection for efficient loss of plasmids or integrated constructs from yeast during growth on galactose medium, indicating that this system can be used for plasmid shuffling, gene replacements and marker gene recycling. This counter-selection system has wide application, because any Gal+ strain and a wide variety of marker genes can be used. In addition, counter-selection systems using growth-inhibitory sequences should be applicable to other yeasts and possibly to other organisms.

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Year:  1999        PMID: 10028180     DOI: 10.1002/(SICI)1097-0061(19990115)15:1<1::AID-YEA335>3.0.CO;2-9

Source DB:  PubMed          Journal:  Yeast        ISSN: 0749-503X            Impact factor:   3.239


  4 in total

1.  Isolation of auxotrophic mutants of diploid industrial yeast strains after UV mutagenesis.

Authors:  Shinji Hashimoto; Mayumi Ogura; Kazuo Aritomi; Hisashi Hoshida; Yoshinori Nishizawa; Rinji Akada
Journal:  Appl Environ Microbiol       Date:  2005-01       Impact factor: 4.792

2.  Identification of novel mutations in ACT1 and SLA2 that suppress the actin-cable-overproducing phenotype caused by overexpression of a dominant active form of Bni1p in Saccharomyces cerevisiae.

Authors:  Shiro Yoshiuchi; Takaharu Yamamoto; Hiroshi Sakane; Jun Kadota; Junko Mochida; Masahiro Asaka; Kazuma Tanaka
Journal:  Genetics       Date:  2006-03-17       Impact factor: 4.562

3.  Precise genome-wide base editing by the CRISPR Nickase system in yeast.

Authors:  Atsushi Satomura; Ryosuke Nishioka; Hitoshi Mori; Kosuke Sato; Kouichi Kuroda; Mitsuyoshi Ueda
Journal:  Sci Rep       Date:  2017-05-18       Impact factor: 4.379

4.  A new strategy for seamless gene editing and marker recycling in Saccharomyces cerevisiae using lethal effect of Cwp1.

Authors:  Yuxiao Hu; Yanrong Jia; Xiangdong Zhao; Zihao Yang; Zhimin Hao; Jingao Dong; Fanli Zeng
Journal:  Microbiologyopen       Date:  2018-10-11       Impact factor: 3.139

  4 in total

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