<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE329nnn/GSE329250/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Solanum lycopersicum</species><gds_type>Genome binding/occupancy profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE329250</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>DNA hypomethylation enables the transcriptional repressor SlSPL-CNR to control fruit flavor ester biosynthesis</name><description>DNA hypomethylation is traditionally associated with gene activation. Here we show that DNA hypomethylation permits the binding of a transcriptional repressor SlSPL-CNR, leading to gene silencing in tomato. SlSPL-CNR exhibits methylation-sensitive DNA binding and preferentially occupies unmethylated GTACGG motifs. During fruit ripening, SlDML2-mediated DNA demethylation at the SlAAT1 promoter allows SlSPL-CNR binding, which represses SlAAT1 expression and modulates the biosynthesis of fruit flavor esters. Structural analysis reveals that cytosine methylation introduces a steric clash with Gln94 in the SBP domain. CRISPR knockout of SlSPL-CNR de-represses SlAAT1 and increases ester accumulation. This methylation-sensitive binding is conserved across SBP domain proteins from rice, maize, and tomato. Our findings reveal a mechanism where DNA hypomethylation facilitates repressor recruitment, linking epigenetic dynamics to metabolic control in plants.</description><dates><publication>2026/06/18</publication></dates><accession>GSE329250</accession><cross_references><GSE>329250</GSE><taxon>Solanum lycopersicum</taxon></cross_references></HashMap>