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人巨细胞病毒抑制端锚聚合酶的聚腺苷酸化核糖基化活性——一种抑制Wnt信号通路的潜在策略。

Human Cytomegalovirus Inhibits the PARsylation Activity of Tankyrase--A Potential Strategy for Suppression of the Wnt Pathway.

作者信息

Roy Sujayita, Liu Fengjie, Arav-Boger Ravit

机构信息

Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore 21287, MD, USA.

出版信息

Viruses. 2015 Dec 29;8(1):8. doi: 10.3390/v8010008.

Abstract

Human cytomegalovirus (HCMV) was reported to downregulate the Wnt/β-catenin pathway. Induction of Axin1, the negative regulator of the Wnt pathway, has been reported as an important mechanism for inhibition of β-catenin. Since Tankyrase (TNKS) negatively regulates Axin1, we investigated the effect of HCMV on TNKS expression and poly-ADP ribose polymerase (PARsylation) activity, during virus replication. Starting at 24 h post infection, HCMV stabilized the expression of TNKS and reduced its PARsylation activity, resulting in accumulation of Axin1 and reduction in its PARsylation as well. General PARsylation was not changed in HCMV-infected cells, suggesting specific inhibition of TNKS PARsylation. Similarly, treatment with XAV939, a chemical inhibitor of TNKS' activity, resulted in the accumulation of TNKS in both non-infected and HCMV-infected cell lines. Reduction of TNKS activity or knockdown of TNKS was beneficial for HCMV, evidenced by its improved growth in fibroblasts. Our results suggest that HCMV modulates the activity of TNKS to induce Axin1, resulting in inhibition of the β-catenin pathway. Since HCMV replication is facilitated by TNKS knockdown or inhibition of its activity, TNKS may serve as an important virus target for control of a variety of cellular processes.

摘要

据报道,人巨细胞病毒(HCMV)可下调Wnt/β-连环蛋白信号通路。Wnt信号通路的负调节因子Axin1的诱导被认为是抑制β-连环蛋白的重要机制。由于端锚聚合酶(TNKS)对Axin1起负调节作用,我们研究了HCMV在病毒复制过程中对TNKS表达和多聚ADP核糖聚合酶(PAR化)活性的影响。感染后24小时起,HCMV使TNKS的表达稳定,并降低其PAR化活性,导致Axin1积累且其PAR化水平也降低。HCMV感染的细胞中总的PAR化水平未改变,提示对TNKS的PAR化存在特异性抑制。同样,用TNKS活性的化学抑制剂XAV939处理,导致未感染和HCMV感染的细胞系中TNKS均积累。TNKS活性降低或敲低对HCMV有利,这在其在成纤维细胞中生长改善得到证明。我们的结果提示,HCMV调节TNKS的活性以诱导Axin1,从而抑制β-连环蛋白信号通路。由于TNKS敲低或其活性抑制可促进HCMV复制,TNKS可能是控制多种细胞过程的重要病毒靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b39/4728568/892e5ee4bc69/viruses-08-00008-g001a.jpg

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