Giri Bikash Ranjan, Du Xiaoli, Xia Tianqi, Chen Yongjun, Li Hao, Cheng Guofeng
Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Key Laboratory of Animal Parasitology, Ministry of Agriculture, 518 Ziyue Road, Shanghai, 200241, China.
Parasitol Res. 2017 Jul;116(7):1947-1954. doi: 10.1007/s00436-017-5476-0. Epub 2017 May 30.
Pluripotent stem cells, called neoblasts, are well known for the regenerative capability and developmental plasticity in flatworms. Impressive advancement has been made in free-living flatworms, while in case of its parasitic counterpart, neoblast-like stem cells have attracted recent attention for its self-renewal and differentiation capacity. Nanos is a key conserved post-transcriptional regulator critical for the formation, development, and/or maintenance of the pluripotent germ line stem cell systems in many metazoans including schistosomes. In the present study, we report the molecular cloning and expression of nanos orthologous genes nanos in Schistosoma japonicum (Sjnanos). The cDNA of Sjnanos is 826 bp long, containing an open reading frame (ORF) for 223 amino acid long protein. qRT-PCR analysis shown that Sjnanos was differently expressed in several stages of schistosomes with relatively high level in schistosomula. Additionally, Sjnanos was expressed highly in adult females compared to adult males. Transfection of recombinant plasmid for expressing Sjnanos resulted in significant proliferation and increased expression of several stem cell factors in mammalian cells. Overall, our preliminary study provides the molecular basis to further functionally characterize Sjnanos in S. japonicum.
多能干细胞,即所谓的新生细胞,以扁形虫的再生能力和发育可塑性而闻名。在自由生活的扁形虫方面已经取得了令人瞩目的进展,而在寄生性扁形虫中,类新生细胞样干细胞因其自我更新和分化能力最近受到了关注。Nanos是一种关键的保守转录后调节因子,对包括血吸虫在内的许多后生动物中多能生殖系干细胞系统的形成、发育和/或维持至关重要。在本研究中,我们报告了日本血吸虫(Sjnanos)中nanos直系同源基因nanos的分子克隆和表达。Sjnanos的cDNA长826 bp,包含一个编码223个氨基酸长蛋白质的开放阅读框(ORF)。qRT-PCR分析表明,Sjnanos在血吸虫的几个阶段中表达不同,在童虫阶段表达水平相对较高。此外,与成年雄虫相比,Sjnanos在成年雌虫中高表达。转染表达Sjnanos的重组质粒导致哺乳动物细胞中几种干细胞因子的显著增殖和表达增加。总体而言,我们的初步研究为进一步在功能上表征日本血吸虫中的Sjnanos提供了分子基础。