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首页> 外文期刊>Molecular Microbiology >Evidence that Plasmodium falciparum chromosome end clusters are cross-linked by protein and are the sites of both virulence gene silencing and activation
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Evidence that Plasmodium falciparum chromosome end clusters are cross-linked by protein and are the sites of both virulence gene silencing and activation

机译:恶性疟原虫染色体末端簇通过蛋白质交联的证据,并且是毒力基因沉默和激活的位点

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摘要

The malaria parasite Plasmodium falciparum undergoes antigenic variation through allelic exclusion and variant expression of surface proteins encoded by the var gene family. Regulation of var genes is under epigenetic control and involves reversible silencing and activation that requires the physical repositioning of a var locus into a transcriptionally permissive zone of the nuclear periphery. P. falciparum chromosome ends appear to aggregate into large perinuclear clusters which house both subtelomeric and chromosome central var genes. In this study we further define the composition of telomeric clusters using fluorescent in situ hybridization, and provide evidence that chromosome end clusters are formed by cross-linking protein. In addition, we demonstrate that a subtelomeric reporter gene and a var gene remain within clusters regardless of their transcriptional status. Our findings support a model whereby a highly localized structure dedicated to the activation of a single var gene can be housed within a gene dense chromosome end cluster that is otherwise transcriptionally silent.
机译:疟原虫恶性疟原虫通过等位基因排斥和由var基因家族编码的表面蛋白的变体表达经历抗原变异。 var基因的调控处于表观遗传控制之下,并且涉及可逆的沉默和激活,这需要将var基因座物理重新定位到核外围的转录允许区域中。恶性疟原虫的染色体末端似乎聚集到大的核周簇中,该簇同时容纳亚端粒和染色体中央var基因。在这项研究中,我们使用荧光原位杂交进一步定义端粒簇的组成,并提供染色体端簇是由交联蛋白形成的证据。此外,我们证明,亚端粒报道基因和var基因保留在群集内,无论它们的转录状态如何。我们的发现支持一种模型,通过该模型,可以将致力于单个var基因激活的高度局部化的结构容纳在基因密集的染色体末端簇中,而该簇在转录上是沉默的。

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