School of Marine Sciences, Ningbo University, Ningbo 315211, China.
School of Marine Sciences, Ningbo University, Ningbo 315211, China.
Gene. 2018 Jul 20;664:101-110. doi: 10.1016/j.gene.2018.04.034. Epub 2018 Apr 22.
Daphnia pulex is an important food organism that exhibits a particular mode of reproduction known as cyclical parthenogenesis (asexual) and sexual reproduction. Regulation of the aging process by microRNAs (miRNAs) is a research hotspot in miRNA studies. To investigate a possible role of miRNAs in regulating aging and senescence, we used Illumina HiSeq to sequence two miRNA libraries from 1-day-old (1d) and 25-day-old (25d) D. pulex specimens. In total, we obtained 11,218,097 clean reads and 28,569 unique miRNAs from 1d specimens and 11,819,106 clean reads and 44,709 unique miRNAs from 25d specimens. Bioinformatic analyses was used to identify 1335 differentially expressed miRNAs from known miRNAs, including 127 miRNAs that exhibited statistically significant differences (P < 0.01); 92 miRNAs were upregulated and 35 were downregulated. Quantitative real-time (qRT)-PCR experiments were performed for nine miRNAs from five samples (1d, 5d, 10d, 15d, 20d and 25d) during the aging process, and the sequencing and qRT-PCR data were found to be consistent. Ninety-four miRNAs were predicted to correspond to 2014 target genes in known miRNAs with 4032 target gene sites. Sixteen pathways changed significantly (P < 0.05) at different developmental stages, revealing many important principles of the miRNA regulatory aging network of D. pulex. Overall, the difference in miRNA expression profile during aging of D. pulex forms a basis for further studies aimed at understanding the role of miRNAs in regulating aging, reproductive transformation, senescence, and longevity.
大型溞是一种重要的食物生物,表现出一种特殊的繁殖方式,称为周期性孤雌生殖(无性)和有性生殖。miRNA 调控衰老过程是 miRNA 研究的一个研究热点。为了研究 miRNA 在调控衰老和衰老中的可能作用,我们使用 Illumina HiSeq 对来自 1 日龄(1d)和 25 日龄(25d)D. pulex 标本的两个 miRNA 文库进行了测序。总共从 1d 标本中获得了 11,218,097 条清洁读取和 28,569 个独特的 miRNA,从 25d 标本中获得了 11,819,106 条清洁读取和 44,709 个独特的 miRNA。生物信息学分析用于从已知的 miRNA 中鉴定出 1335 个差异表达的 miRNA,其中包括 127 个显示出统计学差异(P<0.01)的 miRNA;92 个 miRNA 上调,35 个 miRNA 下调。在衰老过程中,对五个样本(1d、5d、10d、15d、20d 和 25d)中的九个 miRNA 进行了定量实时(qRT)-PCR 实验,测序和 qRT-PCR 数据一致。94 个 miRNA 预测对应于已知 miRNA 中的 2014 个靶基因,有 4032 个靶基因位点。在不同的发育阶段,有 16 条途径发生了显著变化(P<0.05),揭示了 D. pulex 中 miRNA 调控衰老网络的许多重要原则。总的来说,大型溞衰老过程中 miRNA 表达谱的差异为进一步研究 miRNA 在调控衰老、生殖转化、衰老和长寿中的作用奠定了基础。