Guangxi Key Laboratory of Aquatic Genetic Breeding and Healthy Aquaculture, Academy of Fisheries Sciences, Nanning, Guangxi 530021, China.
Guangxi Key Laboratory of Aquatic Genetic Breeding and Healthy Aquaculture, Academy of Fisheries Sciences, Nanning, Guangxi 530021, China.
Comp Biochem Physiol Part D Genomics Proteomics. 2019 Sep;31:100606. doi: 10.1016/j.cbd.2019.100606. Epub 2019 Jul 5.
Crassostrea hongkongensis is one of the three most-commonly cultivated oyster species in China. Although microRNAs (miRNAs) expression in the gonads have been widely investigated, few studies of miRNAs in mollusk gonads are available, particularly in oyster. In the present study, we analyzed the miRNAs expressed in the ovaries and testes of C. hongkongensis. We obtained 14,166,409 and 15,133,900 raw reads from the ovaries and testes, respectively, yielding 13,634,997 (ovarian) and 14,494,149 (testicular) 18-35-nt sequences. We mapped these sequences to the C. hongkongensis genome reference sequence, and identified 8,771,717 (ovarian) and 9,926,014 (testicular) sequences corresponding to miRNAs in the Rfam database. After blasting the miRNA sequences against the miRBase database, we identified 50 known mature miRNAs and 53 novel miRNAs. Of these, 27 miRNAs were significantly upregulated in ovaries as compared to the testes, and 43 miRNAs were significantly upregulated in the testes as compared to the ovaries. To validate the differential expression results generated by Illumina sequencing, we used RT-real-time quantitative PCR (RT-qPCR) to characterize the expression patterns of the six most differently expressed miRNAs (lgi-miR-1990, lgi-miR-1986, lgi-miR-263b, lgi-miR-279, lgi-miR-1992, and novel_98) as well as two miRNAs associated with gonad development (lgi-miR-29 and lgi-miR-8). Most of the RT-qPCR miRNA expression patterns were similar to those recovered by high-throughput sequencing with the exceptions of novel_98 and lgi-miR-1992. Gene Ontology (GO) annotations indicated that the multi-organism cellular process GO category was enriched with the target genes of the differentially expressed miRNAs. Additionally, the target genes were enriched in several KEGG pathways, including the ECM-receptor interaction, galactose metabolism, phagosome, and notch signaling pathway. These pathways are involved in gonadal differentiation and the maintenance of gonad function. This identification and characterization of the miRNAs differentially expressed between the ovaries and testes of C. hongkongensis will increase our understanding of the role of miRNAs in gonad differentiation in the oyster.
中国有三种最常见的养殖牡蛎品种,其中包括太平洋牡蛎。尽管已经广泛研究了性腺中的 microRNAs(miRNAs)表达,但有关软体动物性腺中 miRNAs 的研究很少,尤其是在牡蛎中。在本研究中,我们分析了香港牡蛎性腺中的 miRNAs 表达。我们从卵巢和精巢中分别获得了 14,166,409 和 15,133,900 条原始reads,产生了 13,634,997(卵巢)和 14,494,149(精巢)18-35-nt 序列。我们将这些序列映射到香港牡蛎基因组参考序列上,并在 Rfam 数据库中鉴定出 8,771,717(卵巢)和 9,926,014(精巢)序列对应的 miRNAs。在将 miRNA 序列与 miRBase 数据库进行比对后,我们鉴定出 50 个已知成熟 miRNA 和 53 个新 miRNA。其中,27 个 miRNA 在卵巢中与精巢相比显著上调,43 个 miRNA 在精巢中与卵巢相比显著上调。为了验证 Illumina 测序产生的差异表达结果,我们使用 RT-实时定量 PCR(RT-qPCR)来描述六个表达差异最大的 miRNA(lgi-miR-1990、lgi-miR-1986、lgi-miR-263b、lgi-miR-279、lgi-miR-1992 和 novel_98)以及两个与性腺发育相关的 miRNA(lgi-miR-29 和 lgi-miR-8)的表达模式。除了 novel_98 和 lgi-miR-1992 之外,大多数 RT-qPCR miRNA 表达模式与高通量测序恢复的模式相似。GO 注释表明,多组织细胞过程 GO 类别富含差异表达 miRNA 的靶基因。此外,靶基因富集在几个 KEGG 途径中,包括 ECM-受体相互作用、半乳糖代谢、吞噬体和 notch 信号通路。这些途径参与性腺分化和性腺功能的维持。本研究鉴定和描述了香港牡蛎卵巢和精巢之间差异表达的 miRNAs,将增加我们对 miRNA 在牡蛎性腺分化中的作用的理解。