GCR1 Dependent Transcriptional Activation of Yeast Retrotransposon Ty2-917

Sezai Türkel, Xiao-bei Liao and Philip J. Farabaugh, Yeast, 13:917-930, 1997

Abstract

Transcription of Saccharomyces cerevisiae Ty2-917 retrotransposon depends on regulatory elements both upstream and downstream of the trancription initiation site. An upstream activation sequence (UAS) and a downstream enhancer stimulate transcription synergistically. Here we show that activation by both of these sites depends on the GCR1 product, a transcription factor which also regulates the genes encoding yeast glycolytic enzymes. Eliminating GCR1 causes a 100-fold decrease in transcription of Ty2-917. Activation by the isolated Ty-917 UAS also strongly depends on GCR1. Unexpectedly, GCR1-dependent activation by the Ty2-917 enhancer is strongly position-dependent. Activation by the enhancer in its normal position within the transcription unit depended strongly on GCR1, but eliminating GCR1 reduced activation only 3-fold when the enhancer was moved upstream of the transcribed region. Gel mobility shift and DNase I protection assays indicated that GCR1 binds specifically to multiple sites within the Ty2-917 UAS and enhancer regions. The unexpected position dependence of GCR1 activation suggests that its role may be to overcome the disruptive effect of transcription through the enhancer-bound transcription activation complex.