<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/GSE269nnn/GSE269263/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE269263</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Profile of mineralocorticoid receptor-dependent transcriptome from the mouse aldosterone-sensitive distal nephron</name><description>The mineralocorticoid receptor (MR, Nr3c2) is responsible for aldosterone-regulation of Na+ and K+ balance and blood pressure. We apply RNA-Seq and bioinformatic approaches in isolated tubule segments of MR KO vs. Control mice to understand how aldosterone activates electrogenic Na+- K+ exchange in the aldosterone sensitive distal nephron (ASDN), including connecting tubule and cortical collecting duct tubule. MR-flox/Pax8‐rtTA/LC1 mice were used as a doxycycline (DOX)-inducible Nr3c2 gene KO model. After DOX treatment, four groups were prepared to distinguish between K+ and MR effects: 1) control mice on normal K+ diet (CT-NK) or 2) high K+ diet (CT-HK) and 3) MR knockout mice on normal K+ diet (KO-NK) or 4) low K+ diet (KO-LK). RNA-Seq analysis was carried out in the microdissected connecting tubule and cortical collecting duct tubule segments (5-6 mice per group and ~10 fresh ASDN tubules per mouse). Differential expression (DE) genes were identified (FDR&lt; 0.05) and used for further bioinformatic analyses. DE genes were identified from comparisons of MR KO-NK vs. CT-NK and MR KO-LK vs. CT-HK, respectively. Absence of transcripts on the third exon of Nr3c2 gene confirmed complete disruption of Nr3c2 gene in the MR KO. All known aldosterone-response genes were significantly decreased in MR KO-LK compared to CT-HK. Our data provide a comprehensive MR-dependent transcriptomic profile of the ASDN isolated from the kidney.</description><dates><publication>2026/06/30</publication></dates><accession>GSE269263</accession><cross_references><GSM>GSM8311145</GSM><GSM>GSM8311134</GSM><GSM>GSM8311146</GSM><GSM>GSM8311135</GSM><GSM>GSM8311132</GSM><GSM>GSM8311143</GSM><GSM>GSM8311144</GSM><GSM>GSM8311133</GSM><GSM>GSM8311141</GSM><GSM>GSM8311130</GSM><GSM>GSM8311142</GSM><GSM>GSM8311131</GSM><GSM>GSM8311140</GSM><GSM>GSM8311129</GSM><GSM>GSM8311127</GSM><GSM>GSM8311138</GSM><GSM>GSM8311139</GSM><GSM>GSM8311128</GSM><GSM>GSM8311147</GSM><GSM>GSM8311136</GSM><GSM>GSM8311125</GSM><GSM>GSM8311137</GSM><GSM>GSM8311126</GSM><GPL>21103</GPL><GSE>269263</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>