Li Yao, Li Jialian, Fang Chengchi, Shi Liang, Tan Jiajian, Xiong Yuanzhu, Li Changchun
Key Lab of Agriculture Animal Genetics, Breeding, and Reproduction of Ministry of Education, College of Animal Science and Technology, Huazhong Agricultural University, Wuhan, 430070, People's Republic of China.
Guangxi Yangxiang Pig Gene Technology limited Company, Guigang, 537120, People's Republic of China.
Sci Rep. 2016 May 27;6:26852. doi: 10.1038/srep26852.
Some documented evidences proved small RNAs (sRNA) and targeted genes are involved in mammalian testicular development and spermatogenesis. However, the detailed molecular regulation mechanisms of them remain largely unknown so far. In this study, we obtained a total of 10,716 mRNAs, 67 miRNAs and 16,953 piRNAs which were differentially expressed between LC and LW pig breeds or between the two sexual maturity stages. Of which, we identified 16 miRNAs and 28 targeted genes possibly related to spermatogenesis; 14 miRNA and 18 targeted genes probably associated with cell adhesion related testis development. We also annotated 579 piRNAs which could potentially regulate cell death, nucleosome organization and other basic biology process, which implied that those piRNAs might be involved in sexual maturation difference. The integrated network analysis results suggested that some differentially expressed genes were involved in spermatogenesis through the ECM-receptor interaction, focal adhesion, Wnt and PI3K-Akt signaling pathways, some particular miRNAs have the negative regulation roles and some special piRNAs have the positive and negative regulation roles in testicular development. Our data provide novel insights into the molecular expression and regulation similarities and diversities of spermatogenesis and testicular development in different pig breeds at different stages of sexual maturity.
一些文献证据表明,小RNA(sRNA)及其靶向基因参与哺乳动物睾丸发育和精子发生。然而,到目前为止,它们详细的分子调控机制仍不清楚。在本研究中,我们共获得了10716个mRNA、67个miRNA和16953个piRNA,这些在长白猪和莱芜猪品种之间或两个性成熟阶段之间存在差异表达。其中,我们鉴定出16个可能与精子发生相关的miRNA和28个靶向基因;14个miRNA和18个可能与细胞黏附相关睾丸发育有关的靶向基因。我们还注释了579个可能调控细胞死亡、核小体组织和其他基本生物学过程的piRNA,这表明这些piRNA可能参与性成熟差异。综合网络分析结果表明,一些差异表达基因通过细胞外基质-受体相互作用、粘着斑、Wnt和PI3K-Akt信号通路参与精子发生,一些特定的miRNA具有负调控作用,一些特殊的piRNA在睾丸发育中具有正调控和负调控作用。我们的数据为不同猪品种在不同性成熟阶段精子发生和睾丸发育的分子表达及调控的异同提供了新的见解。