<HashMap><database>GEO</database><scores/><additional><omics_type>Transcriptomics</omics_type><species>Danio rerio</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=GSE310772</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Integrating AI in characterization receptor and construction signaling network for beta-glucan-engaged trained immunity in zebrafish</name><description>Trained immunity, a form of innate immune memory, involves the functional reprogramming of innate immune cells, enabling an enhanced nonspecific response to subsequent challenges. While beta-glucan, a fungal cell wall component, is a known inducer of this process in zebrafish, the specific receptor responsible remains unidentified. Here, we identify C-type lectin domain-containing 1 (CLDC1), designated DrDectin-1, as the pivotal beta-glucan receptor in zebrafish through AI-driven bioinformatic screening based on mammalian Dectin-1. Structural analysis suggests key beta-glucan binding residues (D182, Y183, H184). Using cldc1 knockout zebrafish in beta-glucan training and secondary infection models, combined with RNA-seq, H3K4me3 ChIP-seq, and virtual cell modeling, we demonstrate that CLDC1 mediates trained immunity via the Syk-Raf signaling pathways. Our findings identify the long-sought beta-glucan receptor in zebrafish and provide a comprehensive mechanistic framework for innate immune memory in teleosts, with implications for evolutionary immunology and disease management.</description><dates><publication>2026/06/01</publication></dates><accession>GSE310772</accession><cross_references><GSM>GSM9308641</GSM><GSM>GSM9308637</GSM><GSM>GSM9308636</GSM><GSM>GSM9308639</GSM><GSM>GSM9308638</GSM><GSM>GSM9308640</GSM><GPL>18413</GPL><GSE>310772</GSE><taxon>Danio rerio</taxon></cross_references></HashMap>