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A genome-wide transcriptional analysis identified genes upregulated in response to <I>GTS1</I> induction, most of which were found to be regulated by the Tup1-Cyc8 co-repressor. Among the upregulated genes, <I>FLO1</I> was indispensable for cell aggregation, one of the pleiotropic effects of <I>GTS1</I>. Deletion of genes encoding the chromatin remodeling complex SWI/SNF abolished <I>FLO1</I> upregulation and decreased cell aggregation, although the nuclear localization of Gts1p required for cell aggregation was not affected. <I>GTS1</I> induction caused chromatin remodeling at the <I>FLO1</I> promoter in a SWI/SNF-dependent manner on micrococcal nuclease accessibility assay. Cyc8p was detected in Gts1p-mediated protein aggregates by agarose gel electrophoresis, indicating that Gts1p inhibited Cyc8p function. These results suggest that inhibition of the Tup1-Cyc8 complex and subsequent SWI/SNF-dependent chromatin remodeling result in Gts1p-mediated gene derepression."}],"abstractLicenseFlag":"disallow"}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1410001206479774592","@type":"Researcher","personIdentifier":[{"@type":"NRID","@value":"9000018563678"}],"foaf:name":[{"@language":"en","@value":"SANADA Mitsuaki"}],"jpcoar:affiliationName":[{"@language":"en","@value":"Division of Applied Life Sciences, Graduate School of Agriculture, Kyoto 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