Molecular and General Genetics MGG

, Volume 220, Issue 2, pp 213–221

Ty RNA levels determine the spectrum of retrotransposition events that activate gene expression in Saccharomyces cerevisiae

  • M. Joan Curcio
  • Anne-Marie Hedge
  • Jef D. Boeke
  • David J. Garfinkel
Article

DOI: 10.1007/BF00260484

Cite this article as:
Curcio, M.J., Hedge, A., Boeke, J.D. et al. Molec. Gen. Genet. (1990) 220: 213. doi:10.1007/BF00260484

Summary

To learn more about the variety of Ty elements capable of activating gene expression, we characterized 206 spontaneous Ty transpositions that activate the promoterless gene his3Δ4. Most of the Ty elements appear to be full-length, although a few deleted elements were recovered. Over 95% of the insertions belong to the Ty1 family, and the rest are Ty2 elements. The excessive number of Ty1 transpositions was unexpected because there are only 2-fold more Ty1 than Ty2 elements in the yeast strains used in the selection. However, there is 20-fold more Ty1 than Ty2 RNA present in these yeast strains. This difference in RNA level explains the greater number of Ty1 verses Ty2 transpositions at his3Δ4, because Ty elements transpose through an RNA intermediate. A similar association between the Ty transcript level and transpositional activation of his3Δ4 is obtained in cells expressing GAL1-promoted Ty2-H556 or Ty2-917 elements, but only if the element does not contain a marker. Genetically marked Ty2-H556NEO and-917NEO elements transpose into and activate his3Δ4 with the same efficiency as the previously characterized Ty1H3NEO element, but are underrepresented relative to the levels of TyNEO transcript. We also found that chromosomal Ty transcripts are even more abundant than previously estimated and comprise about 1% of total cellular RNA.

Key words

Ty elementsSaccharomyces cerevisiaeRetrotransposon

Copyright information

© Springer-Verlag 1990

Authors and Affiliations

  • M. Joan Curcio
    • 1
  • Anne-Marie Hedge
    • 1
  • Jef D. Boeke
    • 2
  • David J. Garfinkel
    • 1
  1. 1.BRI-Basic Research ProgramNCI-Frederick Cancer Research FacilityFrederickUSA
  2. 2.Department of Molecular Biology and GeneticsJohns Hopkins School of MedicineBaltimoreUSA