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Updated: Jun 28, 2026

Enhanced Yeast One-hybrid Screens To Identify Transcription Factor Binding To Human DNA Sequences
Published on: February 11, 2019
DNA-binding properties of the yeast Rgt1 repressor
1Mississippi Functional Genomics Network, Department of Biological Sciences, The University of Southern Mississippi, Hattiesburg, 39406, USA. jeongho.kim@mfgn.usm.edu
Abstract:
The yeast HXT (glucose transporter gene) repressor Rgt1 lacks a dimerization domain and thus appears to bind as a monomer to its consensus binding site sequence (5'-CGGANNA-3'). The HXT1 promoter contains 8 Rgt1-binding sites, but its expression is not effectively repressed by Rgt1. In the present study, the Rgt1-binding sites in the HXT1 promoter were analyzed to examine how Rgt1 mediates transcriptional repression. It is seen that Rgt1 binds the HXT1 promoter, but does not significantly mediate repression. When engineered to be multimerized without the intervening sequences between the Rgt1-binding sites, however, 4 or more Rgt1-binding sites were required to provide sufficient Rgt1-dependent repression. These findings suggest that the intervening sequences between the Rgt1-binding sites are important for the regulation of Rgt1 function and that Rgt1 functions efficiently only through multiple binding sites.
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