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ROP18 介导的 HEK293T 细胞转录重编程揭示了 ROP18 在 与宿主细胞相互作用中的新作用。

ROP18-Mediated Transcriptional Reprogramming of HEK293T Cell Reveals New Roles of ROP18 in the Interplay Between and the Host Cell.

机构信息

State Key Laboratory of Veterinary Etiological Biology, Key Laboratory of Veterinary Parasitology of Gansu Province, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, China.

Faculty of Medicine and Health Sciences, School of Veterinary Medicine and Science, University of Nottingham, Loughborough, United Kingdom.

出版信息

Front Cell Infect Microbiol. 2020 Nov 30;10:586946. doi: 10.3389/fcimb.2020.586946. eCollection 2020.

Abstract

secretes a number of virulence-related effector proteins, such as the rhoptry protein 18 (ROP18). To further broaden our understanding of the molecular functions of ROP18, we examined the transcriptional response of human embryonic kidney cells (HEK293T) to ROP18 of type I RH strain. Using RNA-sequencing, we compared the transcriptome of ROP18-expressing HEK293T cells to control HEK293T cells. Our analysis revealed that ROP18 altered the expression of 750 genes (467 upregulated genes and 283 downregulated genes) in HEK293T cells. Gene ontology (GO) and pathway enrichment analyses showed that differentially expressed genes (DEGs) were significantly enriched in extracellular matrix- and immune-related GO terms and pathways. KEGG pathway enrichment analysis revealed that DEGs were involved in several disease-related pathways, such as nervous system diseases and eye disease. ROP18 significantly increased the alternative splicing pattern "retained intron" and altered the expression of 144 transcription factors (TFs). These results provide new insight into how ROP18 may influence biological processes in the host cells altering the expression of genes, TFs, and pathways. More and studies are required to substantiate these findings.

摘要

分泌许多与毒力相关的效应蛋白,如 rhoptry 蛋白 18(ROP18)。为了进一步拓宽我们对 ROP18 分子功能的理解,我们研究了 I 型 RH 株的 ROP18 对人胚肾细胞(HEK293T)的转录反应。我们使用 RNA-seq 比较了 ROP18 表达的 HEK293T 细胞与对照 HEK293T 细胞的转录组。我们的分析表明,ROP18 改变了 HEK293T 细胞中 750 个基因的表达(467 个上调基因和 283 个下调基因)。基因本体论(GO)和途径富集分析表明,差异表达基因(DEGs)在细胞外基质和免疫相关 GO 术语和途径中显著富集。KEGG 途径富集分析表明,DEGs 参与了几种与疾病相关的途径,如神经系统疾病和眼部疾病。ROP18 显著增加了“保留内含子”的选择性剪接模式,并改变了 144 个转录因子(TFs)的表达。这些结果为 ROP18 如何影响宿主细胞中的生物学过程提供了新的见解,改变了基因、TFs 和途径的表达。需要更多的研究来证实这些发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5adc/7734210/78ba3249eeb5/fcimb-10-586946-g001.jpg

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