Gao Yuan, Wu Mingli, Fan Yingzhi, Li Shipeng, Lai Zhenyu, Huang Yongzhen, Lan Xianyong, Lei Chuzhao, Chen Hong, Dang Ruihua
Shaanxi Key Laboratory of Molecular Biology for Agriculture, College of Animal Science and Technology, Northwest A&F University, Yangling 712100, Shaanxi, People's Republic of China.
R Soc Open Sci. 2018 Jul 25;5(7):180413. doi: 10.1098/rsos.180413. eCollection 2018 Jul.
Circular RNA (circRNA) is a new class of non-coding RNA that has recently attracted researchers' interest. Studies have demonstrated that circRNA can function as microRNA sponges or competing endogenous RNAs. Although circRNA has been explored in some species and tissues, the genetic basis of testis development and spermatogenesis in cattle remains unknown. We performed ribo-depleted total RNA-Seq to detect circRNA expression profiles of neonatal (one week old) and adult (4 years old) Qinchuan cattle testes. We obtained 91 112 596 and 80 485 868 clean reads and detected 21 753 circRNAs. A total of 4248 circRNAs were significantly differentially expressed between neonatal and adult cattle testes. Among these circRNAs, 2225 were upregulated, and 2023 were downregulated in adult cattle testis. Genomic feature, length distribution and other characteristics of the circRNAs in cattle testis were studied. Moreover, Gene Ontology and KEGG pathway analyses were performed for source genes of circRNAs. These source genes were mainly involved in tight junction, adherens junction, TGFβ signalling pathway and reproduction, such as and . CircRNA expression patterns were validated by RT-qPCR. Our discoveries provide a solid foundation for the identification and characterization of key circRNAs involved in testis development or spermatogenesis.
环状RNA(circRNA)是一类新型的非编码RNA,最近引起了研究人员的兴趣。研究表明,circRNA可以作为微小RNA海绵或竞争性内源RNA发挥作用。尽管circRNA已在一些物种和组织中得到研究,但牛睾丸发育和精子发生的遗传基础仍然未知。我们进行了核糖体RNA去除的全RNA测序,以检测新生(一周龄)和成年(四岁)秦川牛睾丸的circRNA表达谱。我们分别获得了91112596条和80485868条clean reads,并检测到21753条circRNA。新生和成年牛睾丸之间共有4248条circRNA存在显著差异表达。其中,成年牛睾丸中有2225条circRNA上调,2023条circRNA下调。我们研究了牛睾丸中circRNA的基因组特征、长度分布和其他特性。此外,对circRNA的来源基因进行了基因本体论和KEGG通路分析。这些来源基因主要参与紧密连接、黏附连接、TGFβ信号通路和生殖等过程,例如和。通过RT-qPCR验证了circRNA的表达模式。我们的发现为鉴定和表征参与睾丸发育或精子发生的关键circRNA提供了坚实的基础。