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DNA 拓扑异构酶 II 参与调控贾第虫囊壁蛋白基因和分化。

DNA topoisomerase II is involved in regulation of cyst wall protein genes and differentiation in Giardia lamblia.

机构信息

Department of Parasitology, College of Medicine, National Taiwan University, Taipei, Taiwan, Republic of China.

出版信息

PLoS Negl Trop Dis. 2013 May 16;7(5):e2218. doi: 10.1371/journal.pntd.0002218. Print 2013.

Abstract

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.

摘要

原虫蓝氏贾第鞭毛虫在人体肠道内分化为感染性囊泡,以传播疾病。囊壁蛋白(cwp)基因的表达在囊形成过程中以相似的动力学增加。然而,人们对其基因调控如何共享共同的机制知之甚少。DNA 拓扑异构酶维持基因组 DNA 的正常拓扑结构。它们对于细胞增殖和组织发育是必要的,因为它们参与转录、DNA 复制和染色体浓缩。在蓝氏贾第鞭毛虫基因组中已经鉴定出一种假定的拓扑异构酶 II(topo II)基因。我们询问拓扑异构酶 II 是否可以调节贾第鞭毛虫的囊形成。我们发现 Topo II 存在于细胞核中,其基因在囊形成过程中上调。Topo II 具有典型的 ATPase 和 DNA 切割活性的 II 型拓扑异构酶。突变分析表明,催化重要的 Tyr 残基和切割结构域对于 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测定来确认 Topo II 在体内与 cwp 启动子的结合。有趣的是,Topo II 的过表达增加了 cwp 基因表达和囊形成的水平。微阵列分析鉴定出 Topo II 上调了 cwp 和特定的 vsp 基因的表达。我们还发现,拓扑异构酶 II 抑制剂依托泊苷对贾第鞭毛虫具有生长抑制作用。依托泊苷的添加显著降低了 cwp 基因表达和囊形成的水平。我们的结果表明,拓扑异构酶 II 在进化过程中具有功能保守性,并且拓扑异构酶 II 在诱导 cwp 基因表达中起着重要作用,这是贾第鞭毛虫分化为囊泡的关键。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4311/3656124/ac93bfa6d0ff/pntd.0002218.g001.jpg

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