<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/GSE324nnn/GSE324158/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Other</omics_type><species>Macaca fascicularis</species><gds_type> Genome binding/occupancy profiling by high throughput sequencing</gds_type><gds_type> Expression 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=GSE324158</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Single-cell multi-omic and spatial landscape of primate pineal gland reveals circadian and melatonin regulatory architecture</name><description>The mammalian pineal gland maintains circadian rhythms and homeostasis by secreting melatonin. However, the lack of a cell-resolved regulatory map limits our understanding of how these neuroendocrine functions are orchestrated in primates. Here, we constructed a multi-omics atlas of the Macaca fascicularis pineal gland by integrating snRNA-seq, snATAC-seq, and spatial transcriptomics. We identified pinealocytes as the predominant cell type, alongside six glial and vascular lineages. Chromatin accessibility analysis delineated cell-type-specific regions enriched for melatonin synthesis and phototransduction genes. Notably, we resolved a dual-layer regulatory architecture: while melatonin synthesis programs are robustly organized, circadian clock regulators exhibit a distinct, sparse spatial pattern. Co-expression networks further identified core modules and regulatory hubs—including CRX/OTX2, LHX4, and RORA—that integrate these circadian and light-responsive signals. Cell-cell communication analysis identified signaling axes, such as PTN-ALK/SDC2, RA-RORB, and NRG1-ERBB4, that potentially coordinate this spatial functional organization. Integrating genetic traits showed that sleep and neuropsychiatric risk variants preferentially map to these pineal regulatory modules. Specifically, sleep-associated loci converged on MEIS1-linked elements, while bipolar disorder-associated loci highlighted candidate genes RDH12 and SDK2. Overall, this study reveals the cellular diversity and spatial regulatory logic of the primate pineal gland, providing a foundation for investigating circadian and neuroendocrine regulation in health and disease.</description><dates><publication>2026/04/23</publication></dates><accession>GSE324158</accession><cross_references><GSM>GSM9570177</GSM><GSM>GSM9570178</GSM><GSM>GSM9570179</GSM><GSM>GSM9570180</GSM><GPL>34842</GPL><GPL>28212</GPL><GSE>324158</GSE><taxon>Macaca fascicularis</taxon></cross_references></HashMap>