<HashMap><database>biostudies-literature</database><scores/><additional><submitter>He H</submitter><funding>the Program for Waterfowl Industry Technology System Innovation Team of Sichuan Province</funding><funding>the International Cooperation Project of Sichuan Province</funding><funding>the National Key R&amp;amp;D Program of China</funding><funding>the Innovation and Demonstration of Industry and Education Integration in Feed Industrial Chain Transformation and Upgradation of Sichuan Province</funding><funding>the National Key R&amp;D Program of China</funding><funding>the National Natural Science Foundation of China</funding><pagination>284</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11761271</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(2)</volume><pubmed_abstract>&lt;i>PLIN1&lt;/i>, a member of the PAT family, is expressed in both adipocytes and steroidogenic cells. In this study, we used cell transfection technology combined with transcriptome sequencing to investigate the regulatory mechanism of &lt;i>PLIN1&lt;/i> in goose follicular GCs. Gene Ontology (GO) analysis revealed that in the four groups (phGC: over_vs_over-NC; hGC: over_vs_over-NC; phGC: si_vs_si-NC; hGC: si_vs_si-NC), most differentially expressed genes (DEGs) were significantly enriched (&lt;i>p&lt;/i> &lt; 0.05) in pathways related to biological processes (BPs), particularly those associated with the regulation of cellular lipid metabolism and oxidative stress. KEGG analysis further identified significant enrichment (&lt;i>p&lt;/i> &lt; 0.05) in pathways related to cell apoptosis and the cell cycle. A joint ana</pubmed_abstract><journal>Animals : an open access journal from MDPI</journal><pubmed_title>Transcriptome Analysis Reveals the Molecular Mechanism of PLIN1 in Goose Hierarchical and Pre-Hierarchical Follicle Granulosa Cells.</pubmed_title><pmcid>PMC11761271</pmcid><funding_grant_id>32202676</funding_grant_id><funding_grant_id>2023YFD1300304</funding_grant_id><funding_grant_id>SCCXTD-2024-25</funding_grant_id><funding_grant_id>2022YFH0035</funding_grant_id><funding_grant_id>2212129406</funding_grant_id><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Hu S</pubmed_authors><pubmed_authors>He H</pubmed_authors><pubmed_authors>Lin Y</pubmed_authors><pubmed_authors>Li L</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Liao L</pubmed_authors><pubmed_authors>Xie H</pubmed_authors><pubmed_authors>Xia L</pubmed_authors><pubmed_authors>Hu J</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Han C</pubmed_authors><pubmed_authors>Yuan X</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcriptome Analysis Reveals the Molecular Mechanism of PLIN1 in Goose Hierarchical and Pre-Hierarchical Follicle Granulosa Cells.</name><description>&lt;i>PLIN1&lt;/i>, a member of the PAT family, is expressed in both adipocytes and steroidogenic cells. In this study, we used cell transfection technology combined with transcriptome sequencing to investigate the regulatory mechanism of &lt;i>PLIN1&lt;/i> in goose follicular GCs. Gene Ontology (GO) analysis revealed that in the four groups (phGC: over_vs_over-NC; hGC: over_vs_over-NC; phGC: si_vs_si-NC; hGC: si_vs_si-NC), most differentially expressed genes (DEGs) were significantly enriched (&lt;i>p&lt;/i> &lt; 0.05) in pathways related to biological processes (BPs), particularly those associated with the regulation of cellular lipid metabolism and oxidative stress. KEGG analysis further identified significant enrichment (&lt;i>p&lt;/i> &lt; 0.05) in pathways related to cell apoptosis and the cell cycle. A joint ana</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2026-04-15T03:19:24.454Z</modification><creation>2025-04-05T19:20:04.468Z</creation></dates><accession>S-EPMC11761271</accession><cross_references><pubmed>39858284</pubmed><doi>10.3390/ani15020284</doi></cross_references></HashMap>