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首页> 外文期刊>Biology of Reproduction: Offical Journal of the Society for the Study of Reproduction >Comparative Analysis of Testis Transcriptomes from Triploid and Fertile Diploid Cyprinid Fish
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Comparative Analysis of Testis Transcriptomes from Triploid and Fertile Diploid Cyprinid Fish

机译:三倍体和可育二倍体鲤类鱼类睾丸转录组的比较分析

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The fertility of fish is a key factor in fish breeding. RNA-seq is widely used in high-throughput sequencing and provides a rapid method to examine the molecular mechanisms underlying a biological process. To probe fertility-related molecular mechanisms, we obtained testis transcriptomes from diploid and triploid cyprinid fish and tested for differentially expressed genes (DEGs) in the testis. A total of 6730 transcripts were differentially expressed between the triploid and diploid fish. In these transcripts, 2428 transcripts showed reduced expression and 4302 transcripts were overexpressed in triploid fish compared to the diploid fish. Functional analyses revealed that partial genes related to reproductive, developmental, and locomotion processes, and the axoneme, were differentially expressed in triploid fish relative to diploid fish. Pathway analysis indicated that variations in the gene expression levels of the "ubiquinone and other terpenoid-quinone biosynthesis pathway'' and the "apoptotic pathway'' played a central role in the sterility of triploid male fish. A series of genes (DNAHs, DNAL1, IFTs, and DNAAF1) associated with sperm flagellar assembly and motility, and testis-specific candidate markers (Tcte1, Tekt1, Tekt4, Spag17, Spag5, Spag9a, Spag1b, and Spef2), had low expression levels in the testis of triploid fish. We validated these DEGs in triploid fish using quantitative PCR to quantify expression of eight representative genes. Furthermore, 276 putative transcription factors, 6 chromatin remodeling factors, and 35 transcription cofactors exhibited differential expression in triploid compared to diploid fish. This study provides insight into the regulatory mechanisms causing sterility in male triploid fish.
机译:鱼的繁殖力是鱼育种的关键因素。 RNA-seq被广泛用于高通量测序,并提供了一种快速的方法来检查生物学过程的分子机制。为了探究与生育力有关的分子机制,我们从二倍体和三倍体鲤科鱼类中获得了睾丸转录组,并测试了睾丸中的差异表达基因(DEG)。三倍体和二倍体鱼之间共有6730个转录物差异表达。在这些转录物中,与二倍体鱼类相比,在三倍体鱼类中表达减少了2428个转录物,而4302个转录物则过表达。功能分析表明,与生殖,发育和运动过程以及轴突相关的部分基因在三倍体鱼类中相对于二倍体鱼类差异表达。途径分析表明,“泛醌和其他萜类醌生物合成途径”和“凋亡途径”的基因表达水平的变化在三倍体雄性鱼类的不育中起着核心作用。与精子鞭毛组装和运动相关的一系列基因(DNAHs,DNAL1,IFT和DNAAF1)和睾丸特异的候选标记(Tcte1,Tekt1,Tekt4,Spag17,Spag5,Spag9a,Spag1b和Spef2)具有低表达三倍体鱼类睾丸中的水平。我们使用定量PCR验证了三倍体鱼类中的这些DEG,以量化八个代表性基因的表达。此外,与二倍体鱼类相比,276个假定的转录因子,6个染色质重塑因子和35个转录辅因子在三倍体中表现出差异表达。这项研究为引起雄性三倍体鱼类不育的调控机制提供了见识。

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