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DNA Topoisomerase II Is Involved in Regulation of Cyst Wall Protein Genes and Differentiation in Giardia lamblia

机译:DNA Topoisomerase II参与调控贾第鞭毛虫的囊壁蛋白基因及其分化

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The protozoan Giardia lamblia differentiates into infectious cysts within the human intestinal tract for disease transmission. Expression of the cyst wall protein (cwp) genes increases with similar kinetics during encystation. However, little is known how their gene regulation shares common mechanisms. DNA topoisomerases maintain normal topology of genomic DNA. They are necessary for cell proliferation and tissue development as they are involved in transcription, DNA replication, and chromosome condensation. A putative topoisomerase II (topo II) gene has been identified in the G. lamblia genome. We asked whether Topo II could regulate Giardia encystation. We found that Topo II was present in cell nuclei and its gene was up-regulated during encystation. Topo II has typical ATPase and DNA cleavage activity of type II topoisomerases. Mutation analysis revealed that the catalytic important Tyr residue and cleavage domain are important for Topo II function. We used etoposide-mediated topoisomerase immunoprecipitation assays to confirm the binding of Topo II to the cwp promoters in vivo. Interestingly, Topo II overexpression increased the levels of cwp gene expression and cyst formation. Microarray analysis identified up-regulation of cwp and specific vsp genes by Topo II. We also found that the type II topoisomerase inhibitor etoposide has growth inhibition effect on Giardia. Addition of etoposide significantly decreased the levels of cwp gene expression and cyst formation. Our results suggest that Topo II has been functionally conserved during evolution and that Topo II plays important roles in induction of the cwp genes, which is key to Giardia differentiation into cysts.
机译:原生动物贾第鞭毛虫兰伯氏菌在人肠道内分化成感染性囊肿,以传播疾病。囊壁蛋白(cwp)基因的表达在侵入过程中以相似的动力学增加。然而,鲜为人知的是他们的基因调控如何共享共同的机制。 DNA拓扑异构酶保持基因组DNA的正常拓扑。它们对于细胞增殖和组织发育是必需的,因为它们参与转录,DNA复制和染色体浓缩。在兰氏菌基因组中已鉴定出一个推定的拓扑异构酶II(topo II)基因。我们询问了Topo II是否可以调节贾第鞭毛虫入侵。我们发现Topo II存在于细胞核中,并且在侵入过程中其基因被上调。 Topo II具有典型的II型拓扑异构酶的ATPase和DNA切割活性。突变分析表明,催化的重要Tyr残基和切割结构域对Topo II功能很重要。我们使用依托泊苷介导的拓扑异构酶免疫沉淀试验来确定Topo II与体内cwp启动子的结合。有趣的是,Topo II的过表达增加了cwp基因表达和囊肿形成的水平。微阵列分析确定了Topo II对cwp和特定vsp基因的上调。我们还发现II型拓扑异构酶抑制剂依托泊苷对贾第鞭毛虫具有生长抑制作用。依托泊苷的添加显着降低了cwp基因表达水平和囊肿形成。我们的结果表明,Topo II在进化过程中一直处于功能保守状态,并且Topo II在cwp基因的诱导中起重要作用,而cwp基因是贾第鞭毛虫向囊肿分化的关键。

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