中国畜禽种业 ›› 2026, Vol. 22 ›› Issue (5): 52-60.doi: 10.19543/j.cnki.1673-4556.20260329.003
周宁1,2,3(
), 刘锦玉2, 卢立志2, 曾涛2, 郑嫩珠1, 张钰3, 李丽1(
), 顾天天1,2(
)
Ning Zhou1,2,3(
), Jinyu Liu2, Lizhi Lu2, Tao Zeng2, Nenzhu Zheng1, Yu Zhang3, Li Li1(
), Tiantian Gu1,2(
)
摘要:
目的 该试验旨在研究300日龄和900日龄蛋鸭卵巢组织转录本的差异,并筛选影响卵巢衰老的关键基因或信号通路。 方法 该试验采集300日龄青年蛋鸭和900日龄老年蛋鸭卵巢组织,通过Illumina HiSeq平台进行深度测序,并对差异表达基因(Differentially expressed genes, DEGs)进行基因本体(Gene ontology, GO)功能注释、京都基因与基因组百科全书(Kyoto encyclopedia of genes and genomes, KEGG)富集分析和实时荧光定量PCR(Quantitative Real-time PCR)验证。 结果 结果显示,900日龄和300日龄蛋鸭卵巢间共鉴定出403个基因表达存在显著差异,其中235个上调基因,168个下调基因。GO功能显著富集在代谢过程、免疫系统过程、生殖过程和转录调节活性等条目;KEGG通路显著富集在白细胞介素-17信号通路、ECM受体相互作用和花生四烯酸代谢等通路。qRT-PCR结果发现,10个基因(ADRA2B、TF、APOC3、RXRG、MMP9、GRIA4、OXTR、ATP6V1G3、TRPC5和STMN4)在900日龄和300日龄蛋鸭卵巢组织间表达变化模式与转录组测序结果一致,表明RNA-Seq结果可靠。 结论 转录组测序筛选出403个显著差异基因,其中TF、APOC3、TRPC5等基因可能与卵巢衰老相关。KEGG富集显示的白介素-17信号通路、ECM受体相互作用和花生四烯酸代谢等通路,可影响炎症反应和损伤,参与蛋鸭卵巢衰老。
中图分类号:
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