Fig. 6From: Molecular breeding of Saccharomyces cerevisiae with high RNA content by harnessing essential ribosomal RNA transcription regulatorTranscription level of NTS regions. Transcription level of seven sites within rDNA unit was determined by quantitative real-time PCR. Primer pairs used for detection of each site are listed in Additional file 1: Table S1. White bars; SH8836. Light grey bars Sup16[pRRN5], dark grey bars ∆fob1; Black bars ∆fob1Sup16[pRRN5]. The values are the means and standard deviations of results from three independent experiments. The figure below the graph represents the location of each site in this experimentBack to article page