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Integrated analysis of mRNA and miRNA in testis and cauda epididymidis reveals candidate molecular markers associated with reproduction in Dezhou donkey

机译:Testis和Cauda附睾mRNA和miRNA的综合分析显示与德州驴繁殖相关的候选分子标记

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In China, donkeys are raised for fur, meat, and milk. Reproduction and breeding are crucial to maintain the donkey industry, and conventional breeding is currently applied. This study explored functional factors related to spermatogenesis, maturation, and storage and to identify molecular markers associated with donkey reproduction by analyzing the regulatory elements and target genes in testis and epididymidis. This research is essential to extending donkey genetic information resources and will lay a foundation for molecular breeding. High-throughput sequencing techniques can analyze genetic variations and candidate genes related to different traits. In this study, we identified 6,097 significant differentially expressed genes (DEGs) between testis and cauda epididymidis, including 1,245 transcription factors (TFs). We also found putative SNPs located in coding regions. Alternative splicing events of expressed genes were identified, among which skipping exon and alternative 3' splice site events were the most ubiquitous. We obtained 169 miRNAs that were differentially expressed. 5,285 DE-targets were involved in 286 pathways according to KEGG functional annotations, including focal adhesion, ECM-receptor interaction, actin cytoskeleton regulation, rap1 signaling pathway, and PI3K-Akt signaling pathway possibly related to spermatogenesis. We have distinguished pivotal DEGs (Col6a2, ITGA4, ITGA6, ITGB1, PRKCA, and AKT1), three TFs (COL6A3, AKT1, and KIT), and some miRNAs (miR-141, let-7, miR-148, and miR-221). These high-quality transcriptome and microRNA data of donkey testis and epididymis will facilitate functional studies on the donkey genome. The identified DE-targets and DE-microRNAs are candidate factors for donkey reproduction traits and can be applied to molecular breeding programs.
机译:在中国,驴子饲养毛皮,肉和牛奶。繁殖和育种对于维持驴行业至关重要,目前应用常规育种。本研究探讨了与精子发生,成熟和储存相关的功能因素,并通过分析睾丸和附睾中的调节元素和靶基因来鉴定与驴生殖相关的分子标记。该研究对于扩展驴遗传信息资源至关重要,并将为分子育种奠定基础。高通量测序技术可以分析与不同性状有关的遗传变异和候选基因。在这项研究中,我们确定了睾丸和尾病虫病之间的6,097个显着的差异表达基因(DEG),包括1,245个转录因子(TFS)。我们还发现了位于编码区中的推定SNP。鉴定了表达基因的替代剪接事件,其中跳过外显子和替代的3'剪接部位事件是最无处不在的。我们获得了差异表达的169毫克。根据Kegg功能注释,包括局灶性粘附,ECM-受体相互作用,肌动蛋白细胞骨架调节,RAP1信号通路和PI3K-AKT信号传导途径,包括与精子发生有关的局灶性粘附,包括局灶性粘附,ECM-受体相互作用。我们具有卓越的枢轴(COL6A2,ITGA4,ITGA6,ITGB1,PRKCA和AKT1),三个TFS(COL6A3,AKT1和套件),以及一些MIRNA(MIR-141,Let-7,MIR-148和MIR- 221)。这些高质量的转录组和驴睾丸和附睾的MicroRNA数据将促进对驴基因组的功能研究。所确定的脱靶和DE-MICRRNA是驴再现性状的候选因子,可以应用于分子育种计划。

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