Osman Ahmed, Niles Edward G, Verjovski-Almeida Sergio, LoVerde Philip T
Department of Microbiology and Immunology, School of Medicine and Biomedical Sciences, State University of New York at Buffalo, Buffalo, New York, USA.
PLoS Pathog. 2006 Jun;2(6):e54. doi: 10.1371/journal.ppat.0020054. Epub 2006 Jun 16.
Members of transforming growth factor-beta (TGF-beta) superfamily play pivotal roles in development in multicellular organisms. We report the functional characterization of the Schistosoma mansoni type II receptor (SmTbetaRII). Mining of the S. mansoni expressed sequence tag (EST) database identified an EST clone that shows homology to the kinase domain of type II receptors from different species. The amplified EST sequence was used as a probe to isolate a cDNA clone spanning the entire coding region of a type II serine/threonine kinase receptor. The interaction of SmTbetaRII with SmTbetaRI was elucidated and shown to be dependent on TGF-beta ligand binding. Furthermore, in the presence of human TGF-beta1, SmTbetaRII was able to activate SmTbetaRI, which in turn activated SmSmad2 and promoted its interaction with SmSmad4, proving the transfer of the signal from the receptor complex to the Smad proteins. Gynaecophoral canal protein (GCP), whose expression in male worms is limited to the gynaecophoric canal, was identified as a potential TGF-beta target gene in schistosomes. Knocking down the expression of SmTbetaRII using short interfering RNA molecules (siRNA) resulted in a concomitant reduction in the expression of GCP. These data provide evidence for the direct involvement of SmTbetaRII in mediating TGF-beta-induced activation of the TGF-beta target gene, SmGCP, within schistosome parasites. The results also provide additional evidence for a role for the TGF-beta signaling pathway in male-induced female reproductive development.
转化生长因子-β(TGF-β)超家族成员在多细胞生物的发育过程中发挥着关键作用。我们报告了曼氏血吸虫II型受体(SmTbetaRII)的功能特性。通过对曼氏血吸虫表达序列标签(EST)数据库的挖掘,鉴定出一个EST克隆,它与来自不同物种的II型受体的激酶结构域具有同源性。扩增后的EST序列被用作探针,以分离出一个跨越II型丝氨酸/苏氨酸激酶受体整个编码区的cDNA克隆。阐明了SmTbetaRII与SmTbetaRI的相互作用,并表明其依赖于TGF-β配体结合。此外,在人TGF-β1存在的情况下,SmTbetaRII能够激活SmTbetaRI,进而激活SmSmad2并促进其与SmSmad4的相互作用,证明了信号从受体复合物传递到Smad蛋白。雌虫抱合沟蛋白(GCP)在雄虫中的表达仅限于雌虫抱合沟,被确定为血吸虫中潜在的TGF-β靶基因。使用短干扰RNA分子(siRNA)敲低SmTbetaRII的表达会导致GCP表达随之降低。这些数据为SmTbetaRII直接参与介导TGF-β诱导的血吸虫寄生虫内TGF-β靶基因SmGCP的激活提供了证据。这些结果也为TGF-β信号通路在雄虫诱导雌虫生殖发育中的作用提供了额外证据。