Key Laboratory of Yak Breeding in Gansu Province, Lanzhou Institute of Husbandry and Pharmaceutical Sciences, Chinese Academy of Agricultural Sciences, Lanzhou 730050, China; Key Laboratory of Animal Genetics and Breeding on Tibetan Plateau, Ministry of Agriculture and Rural Affairs, Lanzhou 730050, China.
Key Laboratory of Yak Breeding in Gansu Province, Lanzhou Institute of Husbandry and Pharmaceutical Sciences, Chinese Academy of Agricultural Sciences, Lanzhou 730050, China; Key Laboratory of Animal Genetics and Breeding on Tibetan Plateau, Ministry of Agriculture and Rural Affairs, Lanzhou 730050, China.
Genomics. 2024 Jul;116(4):110872. doi: 10.1016/j.ygeno.2024.110872. Epub 2024 Jun 6.
Cattle-yak is a hybrid offspring resulting from the crossbreeding of yak and cattle, and it exhibits substantial heterosis in production performance. However, male sterility in cattle-yak remains a concern. Reports suggest that noncoding RNAs are involved in the regulation of spermatogenesis. Therefore, in this study, we comprehensively compared testicular transcription profiles among cattle, yak, and cattle-yak. Numerous differentially expressed genes (DEGs), differentially expressed circRNAs (DECs), and differentially expressed miRNAs (DEMs) were identified in the intersection of two comparison groups, namely cattle versus cattle-yak and yak versus cattle-yak, with the number of DEGs, DECs, and DEMs being 4968, 360, and 59, respectively. The DEGs in cattle-yaks, cattle, and yaks were mainly associated with spermatogenesis, male gamete generation, and sexual reproduction. Concurrently, GO and KEGG analyses indicated that DEC host genes and DEM source genes were involved in the regulation of spermatogenesis. The construction of a potential competing endogenous RNA network revealed that some differentially expressed noncoding RNAs may be involved in regulating the expression of genes related to testicular spermatogenesis, including miR-423-5p, miR-449b, miR-34b/c, and miR-15b, as well as previously unreported miR-6123 and miR-1306, along with various miRNA-circRNA interaction pairs. This study serves as a valuable reference for further investigations into the mechanisms underlying male sterility in cattle-yaks.
犏牛是牦牛与黄牛杂交的后代,具有明显的杂种优势生产性能。然而,犏牛的雄性不育问题仍然存在。有报道称,非编码 RNA 参与了精子发生的调控。因此,在这项研究中,我们综合比较了犏牛、牦牛和黄牛睾丸转录组谱。在牛与犏牛和牦牛与犏牛的两个比较组的交集,鉴定出大量差异表达基因(DEGs)、差异表达环状 RNA(DECs)和差异表达 miRNA(DEMs),其中 DEGs、DECs 和 DEMs 的数量分别为 4968、360 和 59。犏牛、牛和牦牛中的 DEGs 主要与精子发生、雄性配子生成和有性生殖有关。同时,GO 和 KEGG 分析表明,DECs 的宿主基因和 DEMs 的来源基因参与了精子发生的调控。一个潜在的竞争性内源 RNA 网络的构建表明,一些差异表达的非编码 RNA 可能参与调节与睾丸精子发生相关的基因的表达,包括 miR-423-5p、miR-449b、miR-34b/c 和 miR-15b,以及之前未报道的 miR-6123 和 miR-1306,以及各种 miRNA-circRNA 相互作用对。这项研究为进一步研究犏牛雄性不育的机制提供了有价值的参考。