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人神经嗜性多瘤病毒,JC 病毒,晚期编码区编码一种新型核蛋白,ORF4,其靶向早幼粒细胞白血病核体(PML-NBs)并调节其重组。

Human neurotropic polyomavirus, JC virus, late coding region encodes a novel nuclear protein, ORF4, which targets the promyelocytic leukemia nuclear bodies (PML-NBs) and modulates their reorganization.

机构信息

Department of Microbiology, Immunology, and Inflammation, Laboratory of Molecular Neurovirology, MERB-757, Lewis Katz School of Medicine at Temple University, 3500 N. Broad Street, Philadelphia, PA 19140, USA.

The Wistar Institute Proteomics and Metabolomics Facility Room 252, 3601 Spruce Street, Philadelphia, PA 19104, USA.

出版信息

Virology. 2023 Oct;587:109866. doi: 10.1016/j.virol.2023.109866. Epub 2023 Aug 19.

Abstract

We previously reported the discovery and characterization of two novel proteins (ORF1 and ORF2) generated by the alternative splicing of the JC virus (JCV) late coding region. Here, we report the discovery and partial characterization of three additional novel ORFs from the same coding region, ORF3, ORF4 and ORF5, which potentially encode 70, 173 and 265 amino acid long proteins respectively. While ORF3 protein exhibits a uniform distribution pattern throughout the cells, we were unable to detect ORF5 expression. Surprisingly, ORF4 protein was determined to be the only JCV protein specifically targeting the promyelocytic leukemia nuclear bodies (PML-NBs) and inducing their reorganization in nucleus. Although ORF4 protein has a modest effect on JCV replication, it is implicated to play major roles during the JCV life cycle, perhaps by regulating the antiviral response of PML-NBs against JCV infections and thus facilitating the progression of the JCV-induced disease in infected individuals.

摘要

我们之前报道了通过 JC 病毒(JCV)晚期编码区的选择性剪接发现并鉴定了两种新型蛋白(ORF1 和 ORF2)。在这里,我们报道了从同一编码区发现并部分鉴定了另外三个新的 ORF,ORF3、ORF4 和 ORF5,它们分别可能编码 70、173 和 265 个氨基酸长的蛋白质。虽然 ORF3 蛋白在细胞中呈现均匀的分布模式,但我们无法检测到 ORF5 的表达。令人惊讶的是,ORF4 蛋白被确定为唯一一种专门针对早幼粒细胞白血病核体(PML-NBs)并诱导其在核内重组的 JCV 蛋白。虽然 ORF4 蛋白对 JCV 复制的影响不大,但它可能在 JCV 生命周期中发挥主要作用,也许是通过调节 PML-NBs 对 JCV 感染的抗病毒反应,从而促进感染个体中 JCV 诱导疾病的进展。

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