Hu Shanming, Chen Songqin, Zhu Haotian, Wang Yanan, Zhou Yongzhi, Cao Jie, Zhang Houshuang, Zhou Jinlin
Key Laboratory of Animal Parasitology of Ministry of Agriculture, Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai, China.
College of Animal Science and Technology, Anhui Agricultural University, Hefei, China.
Front Cell Infect Microbiol. 2025 Apr 30;15:1573239. doi: 10.3389/fcimb.2025.1573239. eCollection 2025.
The salivary glands of female ticks rapidly degenerate after feeding. The mechanism involves programmed cell death mediated by an ecdysteroid receptor. A competing endogenous RNA (ceRNA) network has been established using miRNA and the competitive binding of three types of RNA (lncRNA, circRNA, and mRNA), that were demonstrated to be involved in the regulation of biological processes. However, the comprehensive expression profile and competing endogenous RNA (ceRNA) regulatory network between mRNAs and ncRNAs involved in salivary gland development remain unclear.
In the current study, we employed whole-transcriptome sequencing (RNA sequencing) at various stages of feeding to identify differentially expressed lncRNAs, circRNAs, miRNAs, and mRNAs. The ceRNA networks combining lncRNAs, circRNAs, miRNAs, and mRNAs were predicted and constructed based on the miRanda and TargetScan databases. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were performed for target mRNAs with significantly different expression levels.
We identified several pathways related to organ growth and development: Insulin secretion, the Hippo signaling pathway, the Pl3K-Akt signaling pathway, the FoxO signaling pathway, and the Ferroptosis pathway in the lncRNA-miRNA-mRNA network, and Steroid biosynthesis, Cholesterol metabolism, the FoxO signaling pathway, and the Ferroptosis pathway in the circRNA-miRNA-mRNA network, each of which involved insulin and ecdysteroid regulation.
Our findings have advanced our understanding of the underlying mechanisms of salivary gland development and degeneration.
雌性蜱虫的唾液腺在进食后会迅速退化。其机制涉及由蜕皮甾体受体介导的程序性细胞死亡。利用微小RNA(miRNA)以及三种RNA(长链非编码RNA、环状RNA和信使RNA)的竞争性结合建立了一个竞争性内源RNA(ceRNA)网络,这些RNA被证明参与生物过程的调控。然而,参与唾液腺发育的信使RNA和非编码RNA之间的综合表达谱以及竞争性内源RNA(ceRNA)调控网络仍不清楚。
在本研究中,我们在进食的各个阶段采用全转录组测序(RNA测序)来鉴定差异表达的长链非编码RNA、环状RNA、微小RNA和信使RNA。基于miRanda和TargetScan数据库预测并构建了结合长链非编码RNA、环状RNA、微小RNA和信使RNA的ceRNA网络。对表达水平有显著差异的靶信使RNA进行基因本体(GO)和京都基因与基因组百科全书(KEGG)通路分析。
我们在长链非编码RNA-微小RNA-信使RNA网络中鉴定出了几个与器官生长和发育相关的通路:胰岛素分泌、Hippo信号通路、磷脂酰肌醇-3激酶-蛋白激酶B信号通路、叉头框O信号通路和铁死亡通路;在环状RNA-微小RNA-信使RNA网络中鉴定出了类固醇生物合成、胆固醇代谢、叉头框O信号通路和铁死亡通路,每条通路都涉及胰岛素和蜕皮甾体的调控。
我们的研究结果加深了我们对唾液腺发育和退化潜在机制的理解。