MicroRNA-1 targets ribosomal protein genes to regulate the growth, development and reproduction of Schistosoma japonicum

IF 3.7 2区 医学 Q1 PARASITOLOGY International journal for parasitology Pub Date : 2023-10-01 DOI:10.1016/j.ijpara.2023.03.007
Chengsong Sun , Fang Luo , Yanmin You , Mengjie Gu , Wenbin Yang , Cun Yi , Wei Zhang , Zheng Feng , Jipeng Wang , Wei Hu
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Abstract

Eggs laid by mature female schistosomes are primarily responsible for the pathogenesis of schistosomiasis and critical for transmission. Consequently, elucidating the mechanism of sexual maturation as well as egg production may lead to new strategies for the control of schistosomiasis. MicroRNAs (miRNAs) are involved in multiple biological processes including reproduction in many organisms, yet their roles have not been well characterized in schistosomes. Here, we investigated microRNA-1 (miR-1), which was downregulated gradually in both male and female Schistosoma japonicum after they reached sexually maturity. The expression of miR-1, as shown with quantitative reverse transcription PCR (qRT-PCR), was lower in the reproductive organs of adult females compared with the somatic tissues. Overexpression of miR-1 in adult worms destroyed the morphological architecture of reproductive organs and reduced the subsequent oviposition, which may be due to the activation of apoptosis pathways. Through in silico analysis, 34 potential target genes of miR-1 were identified, including five ribosomal protein genes, called rp-s13, rp-l7ae, rp-l14, rp-l11 and rp-s24e. In vitro dual-luciferase reporter gene assays and miRNA overexpression experiments further validated that these ribosomal protein genes were directly regulated by miR-1. In contrast to the gene expression of miR-1, qRT-PCR and in situ hybridization experiments demonstrated these ribosomal protein genes were enriched in the sexual organs of adult females. Using RNA interference to silence the ribosomal protein genes in different developmental stages in a mouse model system, we demonstrated that these miR-1 target genes not only participated in the reproductive development of S. japonicum, but also were required for the growth and survival of the parasite in the early developmental stages. Taken together, our data suggested that miR-1 may affect the growth, reproduction and oviposition of S. japonicum by targeting the ribosomal protein genes, which provides insights for exploration of new anti-schistosome strategies.

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MicroRNA-1靶向核糖体蛋白基因调控日本血吸虫生长发育和繁殖
成熟雌性血吸虫产卵是血吸虫病发病机制的主要原因,也是传播的关键。因此,阐明性成熟和卵子生产的机制可能会为控制血吸虫病带来新的策略。微小RNA(miRNA)参与多种生物学过程,包括在许多生物体中的繁殖,但它们在血吸虫中的作用尚未得到很好的表征。在这里,我们研究了微小RNA-1(miR-1),它在雄性和雌性日本血吸虫性成熟后逐渐下调。如定量逆转录聚合酶链式反应(qRT-PCR)所示,miR-1在成年雌性生殖器官中的表达低于体细胞组织。miR-1在成虫中的过表达破坏了生殖器官的形态结构,并减少了随后的产卵,这可能是由于细胞凋亡途径的激活。通过计算机分析,鉴定出34个miR-1的潜在靶基因,包括5个核糖体蛋白基因,分别为rp-s13、rp-l7ae、rp-l14、rp-l11和rp-s24e。体外双荧光素酶报告基因测定和miRNA过表达实验进一步验证了这些核糖体蛋白基因受miR-1的直接调控。与miR-1的基因表达相反,qRT-PCR和原位杂交实验表明,这些核糖体蛋白基因在成年女性的性器官中富集。在小鼠模型系统中,利用RNA干扰沉默不同发育阶段的核糖体蛋白基因,我们证明这些miR-1靶基因不仅参与了日本血吸虫的生殖发育,而且是寄生虫早期发育阶段生长和生存所必需的。总之,我们的数据表明,miR-1可能通过靶向核糖体蛋白基因来影响日本血吸虫的生长、繁殖和产卵,这为探索新的抗血吸虫策略提供了见解。
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来源期刊
CiteScore
8.40
自引率
2.50%
发文量
76
审稿时长
23 days
期刊介绍: International Journal for Parasitology offers authors the option to sponsor nonsubscriber access to their articles on Elsevier electronic publishing platforms. For more information please view our Sponsored Articles page. The International Journal for Parasitology publishes the results of original research in all aspects of basic and applied parasitology, including all the fields covered by its Specialist Editors, and ranging from parasites and host-parasite relationships of intrinsic biological interest to those of social and economic importance in human and veterinary medicine and agriculture.
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