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蛙病毒 3 开放阅读框 97R 定位于内质网并诱导核内陷。

Frog virus 3 open reading frame 97R localizes to the endoplasmic reticulum and induces nuclear invaginations.

机构信息

Department of Biology, Trent University, Peterborough, Ontario, Canada.

出版信息

J Virol. 2013 Aug;87(16):9199-207. doi: 10.1128/JVI.00637-13. Epub 2013 Jun 12.

DOI:10.1128/JVI.00637-13
PMID:23760249
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3754063/
Abstract

Frog virus 3 (FV3) is the type species of the genus Ranavirus, family Iridoviridae. The genome of FV3 is 105,903 bases in length and encodes 97 open reading frames (ORFs). The FV3 ORF 97R contains a B-cell lymphoma 2 (Bcl-2) homology 1 (BH1) domain and has sequence similarity to the myeloid cell leukemia-1 (Mcl-1) protein, suggesting a potential role in apoptosis. To begin to understand the role of 97R, we characterized 97R through immunofluorescence and mutagenesis. Here we demonstrated that 97R localized to the endoplasmic reticulum (ER) at 24 h posttransfection. However, at 35 h posttransfection, 97R localized to the ER but also began to form concentrated pockets continuous with the nuclear membrane. After 48 h posttransfection, 97R was still localized to the ER, but we began to observe the ER and the outer nuclear membrane invaginating into the nucleus. To further explore 97R targeting to the ER, we created a series of C-terminal transmembrane domain deletion mutants. We found that deletion of 29 amino acids from the C terminus of 97R abolished localization to the ER. In contrast, deletion of 12 amino acids from the C terminus of 97R did not affect 97R localization to the ER. In addition, a hybrid protein containing the 97R C-terminal 33 amino acids was similarly targeted to the ER. These data indicate that the C-terminal 33 amino acids of 97R are necessary and sufficient for ER targeting.

摘要

蛙病毒 3(FV3)是虹彩病毒科虹彩病毒属的模式种。FV3 的基因组长度为 105903 个碱基,编码 97 个开放阅读框(ORF)。FV3 的 ORF97R 含有一个 B 细胞淋巴瘤 2(Bcl-2)同源 1(BH1)结构域,与髓样细胞白血病-1(Mcl-1)蛋白具有序列相似性,表明其在凋亡中可能具有潜在作用。为了开始了解 97R 的作用,我们通过免疫荧光和突变分析对其进行了表征。在这里,我们证明 97R 在转染后 24 小时定位于内质网(ER)。然而,在转染后 35 小时,97R 定位于 ER,但也开始形成与核膜连续的浓缩口袋。在转染后 48 小时,97R 仍定位于 ER,但我们开始观察到 ER 和外核膜向内凹陷进入细胞核。为了进一步探索 97R 靶向 ER 的机制,我们构建了一系列 C 端跨膜结构域缺失突变体。我们发现,97R C 端 29 个氨基酸的缺失会使其失去定位于 ER 的能力。相比之下,97R C 端 12 个氨基酸的缺失不会影响 97R 定位于 ER。此外,含有 97R C 端 33 个氨基酸的杂合蛋白也被靶向到 ER。这些数据表明,97R 的 C 端 33 个氨基酸是 ER 靶向所必需和充分的。

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