首页> 外文期刊>Journal of Molecular Biology >PfMyb1, a Plasmodium falciparum transcription factor, is required for intra-erythrocytic growth and controls key genes for cell cycle regulation
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PfMyb1, a Plasmodium falciparum transcription factor, is required for intra-erythrocytic growth and controls key genes for cell cycle regulation

机译:PfMyb1,恶性疟原虫转录因子,是促红细胞内生长所需的,它控制细胞周期调控的关键基因

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摘要

During the complex life cycle of Plasmodium falciparum, divided between mosquito and human hosts, the regulation of morphologic changes implies a fine control of transcriptional regulation. Transcriptional control, however, and in particular its molecular actors, transcription factors and regulatory motifs, are as yet poorly described in Plasmodium. In order to decipher the molecular mechanisms implicated in transcriptional regulation, a transcription factor belonging to the tryptophan cluster family was studied. In a previous work, the PfMyb1 protein, contained in nuclear extracts, was shown to have DNA binding activity and to interact specifically with myb regulatory elements. We used long pfmyb1 double-stranded RNA (dsRNA) to interfere with the cognate messenger expression. Parasite cultures treated with pfmyb1 dsRNA exhibited a 40% growth inhibition when compared with either untreated cultures or cultures treated with unrelated dsRNA, and parasite mortality occurred during trophozoite to schizont transition. In addition, the pfmyb1 transcript and protein decreased by as much as 80% in treated trophozoite cultures at the time of their maximum expression. The global effect of this partial loss of transcript and protein was investigated using a thematic DNA microarray encompassing genes involved in signal transduction, cell cycle and transcriptional regulation. SAM software enabled us to identify several genes that were differentially expressed and probably directly or indirectly under the control of PfMyb1. Using chromatin immunoprecipitation, we demonstrated that PfMyb1 binds, within the parasite nuclei, to several promoters and therefore participates directly in the transcriptional regulation of the corresponding genes. This study provides the first evidence of a regulation network involving a Plasmodium transcription factor. (C) 2004 Elsevier Ltd. All rights reserved.
机译:在恶性疟原虫的复杂生命周期中(分为蚊子和人宿主),形态变化的调控意味着对转录调控的良好控制。然而,在疟原虫中,转录控制,特别是其分子演员,转录因子和调节基序还没有被充分描述。为了破译与转录调控有关的分子机制,研究了一种属于色氨酸簇家族的转录因子。在以前的工作中,核提取物中所含的PfMyb1蛋白显示具有DNA结合活性,并与myb调控元件特异性相互作用。我们使用了长pfmyb1双链RNA(dsRNA)来干扰同源信使表达。与未经处理的培养物或未经无关的dsRNA处理的培养物相比,用pfmyb1 dsRNA处理的寄生虫培养物表现出40%的生长抑制,并且在滋养体向裂殖体过渡期间发生了寄生虫死亡。此外,在处理后的滋养体培养物中,pfmyb1转录本和蛋白质在最大表达时降低了多达80%。使用主题DNA微阵列研究了转录物和蛋白质部分丢失的整体效应,该DNA阵列包含涉及信号转导,细胞周期和转录调控的基因。 SAM软件使我们能够识别几个差异表达的基因,这些基因可能在PfMyb1的控制下直接或间接地表达。使用染色质免疫沉淀,我们证明了PfMyb1在寄生虫核内与几个启动子结合,因此直接参与相应基因的转录调控。该研究提供了涉及疟原虫转录因子的调控网络的第一个证据。 (C)2004 Elsevier Ltd.保留所有权利。

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