<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/GSE106nnn/GSE106278/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Candida albicans</species><gds_type> Genome binding/occupancy profiling by genome tiling array</gds_type><gds_type>Expression profiling by array</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE106278</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>The genomic landscape of the fungal specific SWI/SNF complex subunit, Snf6, in Candida albicans</name><description>We have focused our investigation on the characterization of the role of the fungal specific SWI/SNF subunit, Snf6. Our data show that, although the C. albicans subunit has only limited sequence similarity to other fungal orthologs, Snf6 was copurified with SWI/SNF complex subunits including the catalytic ATPase subunit, Snf2. We show that Snf6 plays a critical role in biological processes that are essential for fungal pathogenesis including carbon metabolic flexibility, stress response and morphogenesis. The Snf6 regulon was determined by combining both genome-wide location (ChIP-chip) and transcriptional profiling (microarrays) to identify targets of the SWI/SNF complex under both yeast- and hyphal-promoting conditions.</description><dates><publication>2017/10/28</publication></dates><accession>GSE106278</accession><cross_references><GSM>GSM2834529</GSM><GSM>GSM2834527</GSM><GSM>GSM2834528</GSM><GSM>GSM2834877</GSM><GSM>GSM2834526</GSM><GSM>GSM2834875</GSM><GSM>GSM2834876</GSM><GSM>GSM2834874</GSM><GSM>GSM2834530</GSM><GPL>10636</GPL><GPL>9818</GPL><GSE>106278</GSE><taxon>Candida albicans</taxon><PMID>[29152582]</PMID></cross_references></HashMap>