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曼氏血吸虫锌指蛋白 SmZF1 的分子特征作为一种转录因子。

Molecular characterization of the Schistosoma mansoni zinc finger protein SmZF1 as a transcription factor.

机构信息

Laboratório de Genética Bioquímica, Departamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.

出版信息

PLoS Negl Trop Dis. 2009 Nov 10;3(11):e547. doi: 10.1371/journal.pntd.0000547.

Abstract

BACKGROUND

During its development, the parasite Schistosoma mansoni is exposed to different environments and undergoes many morphological and physiological transformations as a result of profound changes in gene expression. Characterization of proteins involved in the regulation of these processes is of importance for the understanding of schistosome biology. Proteins containing zinc finger motifs usually participate in regulatory processes and are considered the major class of transcription factors in eukaryotes. It has already been shown, by EMSA (Eletrophoretic Mobility Shift Assay), that SmZF1, a S. mansoni zinc finger (ZF) protein, specifically binds both DNA and RNA oligonucleotides. This suggests that this protein might act as a transcription factor in the parasite.

METHODOLOGY/PRINCIPAL FINDINGS: In this study we extended the characterization of SmZF1 by determining its subcellular localization and by verifying its ability to regulate gene transcription. We performed immunohistochemistry assays using adult male and female worms, cercariae and schistosomula to analyze the distribution pattern of SmZF1 and verified that the protein is mainly detected in the cells nuclei of all tested life cycle stages except for adult female worms. Also, SmZF1 was heterologously expressed in mammalian COS-7 cells to produce the recombinant protein YFP-SmZF1, which was mainly detected in the nucleus of the cells by confocal microscopy and Western blot assays. To evaluate the ability of this protein to regulate gene transcription, cells expressing YFP-SmZF1 were tested in a luciferase reporter system. In this system, the luciferase gene is downstream of a minimal promoter, upstream of which a DNA region containing four copies of the SmZF1 putative best binding site (D1-3DNA) was inserted. SmZF1 increased the reporter gene transcription by two fold (p</=0.003) only when its specific binding site was present.

CONCLUSION

Taken together, these results strongly support the hypothesis that SmZF1 acts as a transcription factor in S. mansoni.

摘要

背景

在发育过程中,曼氏血吸虫寄生虫暴露于不同的环境中,并由于基因表达的深刻变化而经历许多形态和生理转化。参与这些过程调节的蛋白质的特征对于理解血吸虫生物学很重要。含有锌指基序的蛋白质通常参与调节过程,并且被认为是真核生物中主要的转录因子类。已经通过 EMSA(电泳迁移率变动测定)表明,曼氏血吸虫锌指(ZF)蛋白 SmZF1 特异性结合 DNA 和 RNA 寡核苷酸。这表明该蛋白可能在寄生虫中作为转录因子发挥作用。

方法/主要发现:在这项研究中,我们通过确定 SmZF1 的亚细胞定位并验证其调节基因转录的能力,扩展了 SmZF1 的特征描述。我们使用成年雄性和雌性蠕虫、尾蚴和毛蚴进行免疫组织化学分析,以分析 SmZF1 的分布模式,并验证该蛋白主要存在于所有测试的生命周期阶段的细胞核中,除了成年雌性蠕虫。此外,SmZF1 在哺乳动物 COS-7 细胞中异源表达以产生重组蛋白 YFP-SmZF1,该蛋白通过共聚焦显微镜和 Western blot 分析主要存在于细胞的细胞核中。为了评估该蛋白调节基因转录的能力,我们在荧光素酶报告基因系统中测试了表达 YFP-SmZF1 的细胞。在该系统中,荧光素酶基因位于最小启动子的下游,在其上游插入了包含 SmZF1 假定最佳结合位点(D1-3DNA)的四个拷贝的 DNA 区域。只有当存在其特异性结合位点时,SmZF1 才使报告基因转录增加两倍(p</=0.003)。

结论

综上所述,这些结果强烈支持 SmZF1 在 S. mansoni 中作为转录因子发挥作用的假设。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d40/2770324/5bf1c9b15afb/pntd.0000547.g001.jpg

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