<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(1)</volume><submitter>Wang D</submitter><pubmed_abstract>Egg-laying performance is of great economic importance in poultry, but the underlying genetic mechanisms are still elusive. In this work, we conduct a multi-omics and multi-tissue integrative study in hens with distinct egg production, to detect the hub candidate genes and construct hub molecular networks contributing to egg-laying phenotypic differences. We identifiy three hub candidate genes as egg-laying facilitators: TFPI2, which promotes the GnRH secretion in hypothalamic neuron cells; CAMK2D, which promotes the FSHβ and LHβ secretion in pituitary cells; and OSTN, which promotes granulosa cell proliferation and the synthesis of sex steroid hormones. We reveal key endocrine factors involving egg production by inter-tissue crosstalk analysis, and demonstrate that both a hepatokine, APOA4, and an adipokine, ANGPTL2, could increase egg production by inter-tissue communication with hypothalamic-pituitary-ovarian axis. Together, These results reveal the molecular mechanisms of multi-tissue coordinative regulation of chicken egg-laying performance and provide key insights to avian reproductive regulation.</pubmed_abstract><journal>Nature communications</journal><pagination>7069</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11329784</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Genome-wide variation study and inter-tissue communication analysis unveil regulatory mechanisms of egg-laying performance in chickens.</pubmed_title><pmcid>PMC11329784</pmcid><pubmed_authors>Tan L</pubmed_authors><pubmed_authors>Bu L</pubmed_authors><pubmed_authors>Li G</pubmed_authors><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Kang X</pubmed_authors><pubmed_authors>Han R</pubmed_authors><pubmed_authors>Guo Y</pubmed_authors><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Dunn IC</pubmed_authors><pubmed_authors>Wang D</pubmed_authors><pubmed_authors>Hu X</pubmed_authors><pubmed_authors>Xu C</pubmed_authors><pubmed_authors>Jiang R</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Zhi Y</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Tian W</pubmed_authors><pubmed_authors>Tian Y</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Xia D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genome-wide variation study and inter-tissue communication analysis unveil regulatory mechanisms of egg-laying performance in chickens.</name><description>Egg-laying performance is of great economic importance in poultry, but the underlying genetic mechanisms are still elusive. In this work, we conduct a multi-omics and multi-tissue integrative study in hens with distinct egg production, to detect the hub candidate genes and construct hub molecular networks contributing to egg-laying phenotypic differences. We identifiy three hub candidate genes as egg-laying facilitators: TFPI2, which promotes the GnRH secretion in hypothalamic neuron cells; CAMK2D, which promotes the FSHβ and LHβ secretion in pituitary cells; and OSTN, which promotes granulosa cell proliferation and the synthesis of sex steroid hormones. We reveal key endocrine factors involving egg production by inter-tissue crosstalk analysis, and demonstrate that both a hepatokine, APOA4, and an adipokine, ANGPTL2, could increase egg production by inter-tissue communication with hypothalamic-pituitary-ovarian axis. Together, These results reveal the molecular mechanisms of multi-tissue coordinative regulation of chicken egg-laying performance and provide key insights to avian reproductive regulation.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2024-12-03T15:08:40.364Z</modification><creation>2024-12-03T15:08:40.364Z</creation></dates><accession>S-EPMC11329784</accession><cross_references><pubmed>39152103</pubmed><doi>10.1038/s41467-024-50809-9</doi></cross_references></HashMap>