Transposon tagging using Ty elements in yeast.
Author(s) -
David Garfinkel,
M F Mastrangelo,
N J Sanders,
B K Shafer,
Jeffrey N. Strathern
Publication year - 1988
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1093/genetics/120.1.95
Subject(s) - transposable element , biology , selectable marker , genetics , gene , mutagenesis , transposon mutagenesis , plasmid , sleeping beauty transposon system , saccharomyces cerevisiae , transposition (logic) , cloning (programming) , yeast , mutation , mutant , linguistics , philosophy , computer science , programming language
We have used the ability to induce high levels of Ty transposition to develop a method for transposon mutagenesis in Saccharomyces cerevisiae. To facilitate genetic and molecular analysis, we have constructed GAL1-promoted TyH3 or Ty917 elements that contain unique cloning sites, and marked these elements with selectable genes. These genes include the yeast HIS3 gene, and the plasmid PiAN7 containing the Tn903 NEO gene. The marked Ty elements retain their ability to transpose, to mutate the LYS2, LYS5, or STE2 genes, and to activate the promoterless his3 delta 4 target gene. Ty elements containing selectable genes are also useful in strain construction, in chromosomal mapping, and in gene cloning strategies.
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