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TRIM21 通过蛋白酶体降解核衣壳蛋白抑制猪流行性腹泻病毒的增殖。

TRIM21 inhibits porcine epidemic diarrhea virus proliferation by proteasomal degradation of the nucleocapsid protein.

机构信息

Department of Swine Infectious Diseases, Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai, People's Republic of China.

Jiangsu Co-Innovation Center for the Prevention and Control of Important Animal Infectious Disease and Zoonose, Yangzhou University, Yangzhou, People's Republic of China.

出版信息

Arch Virol. 2021 Jul;166(7):1903-1911. doi: 10.1007/s00705-021-05080-4. Epub 2021 Apr 26.

Abstract

Tripartite motif protein 21 (TRIM21) is an E3 ubiquitin ligase and cytosolic antibody receptor of the TRIM family. Previous reports have indicated that TRIM21 plays an important role during viral infection. This study aimed at examining the role of TRIM21 in the replication of porcine epidemic diarrhea virus (PEDV) and showed that TRIM21 inhibits PEDV proliferation by targeting and degrading the nucleocapsid (N) protein through the proteasomal pathway. Furthermore, the endogenous expression of TRIM21 was found to be downregulated by PEDV infection in Vero and LLC-PK1 cells. Overexpression of TRIM21 inhibited PEDV replication, whereas knockdown of TRIM21 increased viral titers and N protein levels. TRIM21 was found to interact and colocalize with the N protein, and the TRIM21-mediated antiviral effect was dependent on its ubiquitin ligase activity, which engages in polyubiquitination and degradation of the N protein in a proteasome-dependent manner. Taken together, these findings provide information about the role of TRIM21 in PEDV proliferation and increase our understanding of host-virus interactions.

摘要

三结构域蛋白 21(TRIM21)是一种 E3 泛素连接酶和 TRIM 家族的细胞质抗体受体。先前的研究表明,TRIM21 在病毒感染过程中发挥重要作用。本研究旨在研究 TRIM21 在猪流行性腹泻病毒(PEDV)复制中的作用,并表明 TRIM21 通过蛋白酶体途径靶向和降解核衣壳(N)蛋白来抑制 PEDV 的增殖。此外,研究发现 PEDV 感染可下调 Vero 和 LLC-PK1 细胞中内源性 TRIM21 的表达。TRIM21 的过表达抑制了 PEDV 的复制,而 TRIM21 的敲低则增加了病毒滴度和 N 蛋白水平。发现 TRIM21 与 N 蛋白相互作用并共定位,TRIM21 介导的抗病毒作用依赖于其泛素连接酶活性,该活性通过多泛素化和依赖蛋白酶体的方式降解 N 蛋白。总之,这些发现提供了关于 TRIM21 在 PEDV 增殖中的作用的信息,并增加了我们对宿主-病毒相互作用的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e65b/8074351/daa6317fcd6a/705_2021_5080_Fig1_HTML.jpg

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