Department of Tropical Medicine and Parasitology, College of Medicine, National Taiwan University, Taipei 100, Taiwan, Republic of China.
Department of Medical Research, Taipei Medical University Hospital, Taipei, Taiwan, Republic of China.
Open Biol. 2020 Feb;10(2):190228. doi: 10.1098/rsob.190228. Epub 2020 Feb 5.
causes waterborne diarrhoea by transmission of infective cysts. Three cyst wall proteins are highly expressed in a concerted manner during encystation of trophozoites into cysts. However, their gene regulatory mechanism is still largely unknown. DNA topoisomerases control topological homeostasis of genomic DNA during replication, transcription and chromosome segregation. They are involved in a variety of cellular processes including cell cycle, cell proliferation and differentiation, so they may be valuable drug targets. possesses a type IA DNA topoisomerase (TOP3β) with similarity to the mammalian topoisomerase IIIβ. We found that TOP3β was upregulated during encystation and it possessed DNA-binding and cleavage activity. TOP3β can bind to the promoters using norfloxacin-mediated topoisomerase immunoprecipitation assays. We also found TOP3β can interact with MYB2, a transcription factor involved in the coordinate expression of genes during encystation. Interestingly, overexpression of TOP3β increased expression of - and genes and cyst formation. Microarray analysis confirmed upregulation of and genes by TOP3β. Mutation of the catalytically important Tyr residue, deletion of C-terminal zinc ribbon domain or further deletion of partial catalytic core domain reduced the levels of cleavage activity, and gene expression, and cyst formation. Interestingly, some of these mutant proteins were mis-localized to cytoplasm. Using a CRISPR/Cas9 system for targeted disruption of gene, we found a significant decrease in and gene expression and cyst number. Our results suggest that TOP3β may be functionally conserved, and involved in inducing cyst formation.
通过感染性囊包的传播引起水源性腹泻。在滋养体向囊包转化的过程中,三个囊包壁蛋白以协同的方式高度表达。然而,它们的基因调控机制在很大程度上仍然未知。DNA 拓扑异构酶在复制、转录和染色体分离过程中控制基因组 DNA 的拓扑同质性。它们参与多种细胞过程,包括细胞周期、细胞增殖和分化,因此它们可能是有价值的药物靶点。 含有与哺乳动物拓扑异构酶 IIIβ相似的 IA 型 DNA 拓扑异构酶(TOP3β)。我们发现 TOP3β 在囊包形成过程中上调,并且具有 DNA 结合和切割活性。TOP3β 可以使用诺氟沙星介导的拓扑异构酶免疫沉淀测定与 启动子结合。我们还发现 TOP3β 可以与 MYB2 相互作用,MYB2 是一种转录因子,参与囊包形成过程中 基因的协调表达。有趣的是,TOP3β 的过表达增加了 -和-基因和囊包的表达。微阵列分析证实了 TOP3β 对 和 基因的上调。催化重要的 Tyr 残基的突变、C 端锌指结构域的缺失或部分催化核心结构域的进一步缺失降低了切割活性、 和 基因表达以及囊包形成。有趣的是,这些突变蛋白中的一些错误定位到细胞质中。使用靶向破坏 基因的 CRISPR/Cas9 系统,我们发现 和 基因的表达和囊包数量显著减少。我们的结果表明,TOP3β 可能具有功能保守性,并参与诱导 囊包的形成。