{"title":"Morphological and transcriptional insights into the role of histone phosphorylation-related genes in early development of the chicken duodenum.","authors":"Xiaofeng Li, Bing Yang","doi":"10.5713/ab.25.0108","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To investigate the morphological transitions and the role of histone phosphorylation-related genes during the first week of duodenal development in broilers.</p><p><strong>Methods: </strong>At hatch (D0) and 7 days post-hatch (D7), five broiler chickens were humanely euthanized and duodenal samples were collected to assess the histomorphology, specifically the duodenal villus height (VH), crypt depth (CD), and the VH/CD ratio. The gene expression data of duodenum of broilers at D0 and D7 obtained from the GEO database. Differentially expressed genes (DEG) analyses were conducted using GEO2R. In addition, histone phosphorylation-related genes were obtained from the GeneCards database. Function enrichment for DEGs was conducted using the DAVID and PANTHER databases. Hub genes were identified using the CytoHubba plugin in Cytoscape, employing four different methods: MCON, DNMC, EPC, and MNC. Statistical analyses were conducted using IBM SPSS Statistics.</p><p><strong>Results: </strong>We identified striking developmental transformations: VH surged by 63.02% (P<0.05) and VH/CD ratio doubled (100.68% increase, P<0.05), accompanied by 17.81% CD reduction (P<0.05). Transcriptomic profiling revealed 449 histone phosphorylation-related DEGs, comprising 163 up-regulated and 286 down-regulated candidates. Functional enrichment analysis suggested that these genes participated in phosphorylation, intracellular protein phosphorylation, protein dephosphorylation, immune response, as well as MAPK, PPAR, ErbB, and adipocytokine pathways. Importantly, we identified eight hub genes orchestrating duodenal maturation, including LGALS3, ITGB2, IRF7, SOCS3, and CSF1R, KIF23, SMC2, and DLGAP5.</p><p><strong>Conclusion: </strong>These findings establish a novel paradigm wherein histone phosphorylation coordinates intestinal morphogenesis, providing mechanistic insights for optimizing poultry intestinal health and nutritional strategies.</p>","PeriodicalId":7825,"journal":{"name":"Animal Bioscience","volume":" ","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2025-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Animal Bioscience","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.5713/ab.25.0108","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURE, DAIRY & ANIMAL SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: To investigate the morphological transitions and the role of histone phosphorylation-related genes during the first week of duodenal development in broilers.
Methods: At hatch (D0) and 7 days post-hatch (D7), five broiler chickens were humanely euthanized and duodenal samples were collected to assess the histomorphology, specifically the duodenal villus height (VH), crypt depth (CD), and the VH/CD ratio. The gene expression data of duodenum of broilers at D0 and D7 obtained from the GEO database. Differentially expressed genes (DEG) analyses were conducted using GEO2R. In addition, histone phosphorylation-related genes were obtained from the GeneCards database. Function enrichment for DEGs was conducted using the DAVID and PANTHER databases. Hub genes were identified using the CytoHubba plugin in Cytoscape, employing four different methods: MCON, DNMC, EPC, and MNC. Statistical analyses were conducted using IBM SPSS Statistics.
Results: We identified striking developmental transformations: VH surged by 63.02% (P<0.05) and VH/CD ratio doubled (100.68% increase, P<0.05), accompanied by 17.81% CD reduction (P<0.05). Transcriptomic profiling revealed 449 histone phosphorylation-related DEGs, comprising 163 up-regulated and 286 down-regulated candidates. Functional enrichment analysis suggested that these genes participated in phosphorylation, intracellular protein phosphorylation, protein dephosphorylation, immune response, as well as MAPK, PPAR, ErbB, and adipocytokine pathways. Importantly, we identified eight hub genes orchestrating duodenal maturation, including LGALS3, ITGB2, IRF7, SOCS3, and CSF1R, KIF23, SMC2, and DLGAP5.
Conclusion: These findings establish a novel paradigm wherein histone phosphorylation coordinates intestinal morphogenesis, providing mechanistic insights for optimizing poultry intestinal health and nutritional strategies.
目的:探讨组蛋白磷酸化相关基因在肉仔鸡十二指肠发育第1周的形态转变及其作用。方法:分别于孵化(D0)和孵化后7 d (D7)对5只肉鸡进行人道安乐死,取十二指肠标本,观察十二指肠绒毛高度(VH)、隐窝深度(CD)和VH/CD比值。肉鸡D0和D7时十二指肠基因表达数据来源于GEO数据库。采用GEO2R进行差异表达基因(DEG)分析。此外,从GeneCards数据库中获得组蛋白磷酸化相关基因。使用DAVID和PANTHER数据库对deg进行功能富集。使用Cytoscape中的CytoHubba插件,采用四种不同的方法:MCON、DNMC、EPC和MNC来鉴定枢纽基因。采用IBM SPSS Statistics进行统计分析。结论:这些发现建立了组蛋白磷酸化协调肠道形态发生的新范式,为优化家禽肠道健康和营养策略提供了机制见解。