<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/GSE336nnn/GSE336912/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Arabidopsis thaliana</species><gds_type>Genome binding/occupancy profiling by high throughput sequencing</gds_type><gds_type> Other</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE336912</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Arabidopsis NAC103 (AT5G64060) ChIP-seq and DAP-seq data</name><description>To elucidate the molecular landscape of NAC103-mediated transcriptional regulation in Arabidopsis, we combined chromatin immunoprecipitation sequencing (ChIP-seq) and DNA affinity purification sequencing (DAP-seq) to capture the comprehensive cistrome of NAC103. In this project, we employed the transgenic plants of 35S:NAC103-GFP as the material for ChIP. For DAP-seq, NAC103 protein tagged with Halo (NAC103-Halo) was expressed using Promega’s wheat germ system. These results indicate that NAC103 can directly target promoter regions of ANTHRANILATE SYNTHASE ALPHA SUBUNIT 1 (ASA1, AT5G05730) and Acetyl-coenzyme A Carboxylase 2 (ACC2, AT1G36180).</description><dates><publication>2026/08/04</publication></dates><accession>GSE336912</accession><cross_references><GSM>GSM9844420</GSM><GSM>GSM9844421</GSM><GSM>GSM9844422</GSM><GSM>GSM9844423</GSM><GSM>GSM9844424</GSM><GSM>GSM9844425</GSM><GSM>GSM9844426</GSM><GSM>GSM9844427</GSM><GSM>GSM9844428</GSM><GPL>26208</GPL><GSE>336912</GSE><taxon>Arabidopsis thaliana</taxon></cross_references></HashMap>