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一种新型的 E2F 样蛋白,参与贾第虫囊壁蛋白基因的转录激活。

A novel E2F-like protein involved in transcriptional activation of cyst wall protein genes in Giardia lamblia.

机构信息

Department of Parasitology, College of Medicine, National Taiwan University, Taipei 100, Taiwan.

出版信息

J Biol Chem. 2011 Sep 30;286(39):34101-20. doi: 10.1074/jbc.M111.280206. Epub 2011 Aug 11.

Abstract

Giardia lamblia differentiates into resistant walled cysts for survival outside the host and transmission. During encystation, synthesis of cyst wall proteins is coordinately induced. The E2F family of transcription factors in higher eukaryotes is involved in cell cycle progression and cell differentiation. We asked whether Giardia has E2F-like genes and whether they influence gene expression during Giardia encystation. Blast searches of the Giardia genome database identified one gene (e2f1) encoding a putative E2F protein with two putative DNA-binding domains. We found that the e2f1 gene expression levels increased significantly during encystation. Epitope-tagged E2F1 was found to localize to nuclei. Recombinant E2F1 specifically bound to the thymidine kinase and cwp1-3 gene promoters. E2F1 contains several key residues for DNA binding, and mutation analysis revealed that its binding sequence is similar to those of the known E2F family proteins. The E2F1-binding sequences were positive cis-acting elements of the thymidine kinase and cwp1 promoters. We also found that E2F1 transactivated the thymidine kinase and cwp1 promoters through its binding sequences in vivo. Interestingly, E2F1 overexpression resulted in a significant increase of the levels of CWP1 protein, cwp1-3 gene mRNA, and cyst formation. We also found E2F1 can interact with Myb2, a transcription factor that coordinate up-regulates the cwp1-3 genes during encystation. Our results suggest that E2F family has been conserved during evolution and that E2F1 is an important transcription factor in regulation of the Giardia cwp genes, which are key to Giardia differentiation into cysts.

摘要

蓝氏贾第鞭毛虫在宿主体外和传播过程中分化为具有抗性的囊壁包囊以生存。在囊形成过程中,囊壁蛋白的合成被协调诱导。高等真核生物中的 E2F 转录因子家族参与细胞周期进程和细胞分化。我们想知道蓝氏贾第鞭毛虫是否具有 E2F 样基因,以及它们是否会影响蓝氏贾第鞭毛虫囊形成过程中的基因表达。对蓝氏贾第鞭毛虫基因组数据库的 Blast 搜索鉴定出一个基因(e2f1),其编码一个具有两个推定 DNA 结合结构域的推定 E2F 蛋白。我们发现 e2f1 基因的表达水平在囊形成过程中显著增加。发现标记有表位的 E2F1 定位于细胞核。重组 E2F1 特异性结合胸苷激酶和 cwp1-3 基因启动子。E2F1 包含几个关键的 DNA 结合残基,突变分析表明其结合序列与已知的 E2F 家族蛋白相似。E2F1 结合序列是胸苷激酶和 cwp1 启动子的正向顺式作用元件。我们还发现 E2F1 通过其结合序列在体内反式激活胸苷激酶和 cwp1 启动子。有趣的是,E2F1 过表达导致 CWP1 蛋白、cwp1-3 基因 mRNA 和囊形成水平显著增加。我们还发现 E2F1 可以与 Myb2 相互作用,Myb2 是一种转录因子,它在囊形成过程中协调上调 cwp1-3 基因的表达。我们的结果表明,E2F 家族在进化过程中得到了保守,E2F1 是调节蓝氏贾第鞭毛虫 cwp 基因的重要转录因子,cwp 基因是蓝氏贾第鞭毛虫分化为囊的关键。

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