In Silico Gene Regulatory Network of the Maurer’s Cleft Pathway in Plasmodium falciparum

Itunuoluwa Isewon, Jelili Oyelade, B. Brors, E. Adebiyi
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引用次数: 2

Abstract

The Maurer's clefts (MCs) are very important for the survival of Plasmodium falciparum within an infected cell as they are induced by the parasite itself in the erythrocyte for protein trafficking. The MCs form an interesting part of the parasite's biology as they shed more light on how the parasite remodels the erythrocyte leading to host pathogenesis and death. Here, we predicted and analyzed the genetic regulatory network of genes identified to belong to the MCs using regularized graphical Gaussian model. Our network shows four major activators, their corresponding target genes, and predicted binding sites. One of these master activators is the serine repeat antigen 5 (SERA5), predominantly expressed among the SERA multigene family of P. falciparum, which is one of the blood-stage malaria vaccine candidates. Our results provide more details about functional interactions and the regulation of the genes in the MCs’ pathway of P. falciparum.
恶性疟原虫毛雷尔裂孔通路基因调控网络的研究
毛雷尔裂口(MCs)对恶性疟原虫在感染细胞内的存活非常重要,因为它们是由疟原虫自身在红细胞中诱导的,用于蛋白质运输。MCs形成了寄生虫生物学中一个有趣的部分,因为它们揭示了寄生虫如何重塑红细胞导致宿主发病和死亡。本文采用正则化图形高斯模型对MCs基因的遗传调控网络进行了预测和分析。我们的网络显示了四种主要的激活子、它们对应的靶基因和预测的结合位点。其中一个主激活因子是丝氨酸重复抗原5 (SERA5),主要在恶性疟原虫的SERA多基因家族中表达,是血期疟疾候选疫苗之一。我们的研究结果提供了更多关于恶性疟原虫MCs通路中功能相互作用和基因调控的细节。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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