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本文引用的文献

1
Influenza virus m2 ion channel protein is necessary for filamentous virion formation.流感病毒 M2 离子通道蛋白是丝状病毒粒子形成所必需的。
J Virol. 2010 May;84(10):5078-88. doi: 10.1128/JVI.00119-10. Epub 2010 Mar 10.
2
Influenza C virus NS1 protein upregulates the splicing of viral mRNAs.C 型流感病毒 NS1 蛋白上调病毒 mRNA 的剪接。
J Virol. 2010 Feb;84(4):1957-66. doi: 10.1128/JVI.01627-09. Epub 2009 Dec 9.
3
Influenza A virus lacking M2 protein as a live attenuated vaccine.缺乏M2蛋白的甲型流感病毒作为减毒活疫苗。
J Virol. 2009 Jun;83(11):5947-50. doi: 10.1128/JVI.00450-09. Epub 2009 Mar 25.
4
Site of human rhinovirus RNA uncoating revealed by fluorescent in situ hybridization.荧光原位杂交揭示人鼻病毒RNA脱壳位点
J Virol. 2009 Apr;83(8):3770-7. doi: 10.1128/JVI.00265-08. Epub 2009 Jan 21.
5
Intracellular localization of influenza C virus NS2 protein (NEP) in infected cells and its incorporation into virions.丙型流感病毒NS2蛋白(核输出蛋白)在感染细胞中的细胞内定位及其掺入病毒粒子的情况。
Arch Virol. 2009;154(2):235-43. doi: 10.1007/s00705-008-0292-6. Epub 2009 Jan 8.
6
The influenza virus M2 protein cytoplasmic tail interacts with the M1 protein and influences virus assembly at the site of virus budding.流感病毒M2蛋白的细胞质尾与M1蛋白相互作用,并在病毒出芽位点影响病毒组装。
J Virol. 2008 Oct;82(20):10059-70. doi: 10.1128/JVI.01184-08. Epub 2008 Aug 13.
7
Cytoplasmic domain of influenza B virus BM2 protein plays critical roles in production of infectious virus.乙型流感病毒BM2蛋白的细胞质结构域在传染性病毒的产生中起关键作用。
J Virol. 2008 Jan;82(2):728-39. doi: 10.1128/JVI.01752-07. Epub 2007 Nov 7.
8
Evidence that the CM2 protein of influenza C virus can modify the pH of the exocytic pathway of transfected cells.丙型流感病毒CM2蛋白可改变转染细胞胞吐途径pH值的证据。
J Gen Virol. 2007 Aug;88(Pt 8):2291-2296. doi: 10.1099/vir.0.82785-0.
9
A mutation on influenza C virus M1 protein affects virion morphology by altering the membrane affinity of the protein.丙型流感病毒M1蛋白上的一个突变通过改变该蛋白的膜亲和力来影响病毒粒子形态。
J Virol. 2007 Aug;81(16):8766-73. doi: 10.1128/JVI.00075-07. Epub 2007 May 30.
10
Distinct domains of the influenza a virus M2 protein cytoplasmic tail mediate binding to the M1 protein and facilitate infectious virus production.甲型流感病毒M2蛋白细胞质尾的不同结构域介导与M1蛋白的结合并促进感染性病毒的产生。
J Virol. 2006 Aug;80(16):8178-89. doi: 10.1128/JVI.00627-06.

CM2 蛋白在丙型流感病毒复制周期中的作用。

Role of the CM2 protein in the influenza C virus replication cycle.

机构信息

Department of Infectious Diseases, Yamagata University Faculty of Medicine, 2-2-2 Iida-Nishi, Yamagata 990-9585, Japan.

出版信息

J Virol. 2011 Feb;85(3):1322-9. doi: 10.1128/JVI.01367-10. Epub 2010 Nov 24.

DOI:10.1128/JVI.01367-10
PMID:21106743
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3020500/
Abstract

CM2 is the second membrane protein of influenza C virus. Although its biochemical characteristics, coding strategy, and properties as an ion channel have been extensively studied, the role(s) of CM2 in the virus replication cycle remains to be clarified. In order to elucidate this role, in the present study we generated CM2-deficient influenza C virus-like particles (VLPs) and examined the VLP-producing 293T cells, VLPs, and VLP-infected HMV-II cells. Quantification of viral RNA (vRNA) in the VLPs by real-time PCR revealed that the CM2-deficient VLPs contain approximately one-third of the vRNA found in wild-type VLPs although no significant differences were detected in the expression levels of viral components in VLP-producing cells or in the number and morphology of the generated VLPs. This finding suggests that CM2 is involved in the genome packaging process into VLPs. Furthermore, HMV-II cells infected with CM2-deficient VLPs exhibited significantly reduced reporter gene expression. Although CM2-deficient VLPs could be internalized into HMV-II cells as efficiently as wild-type VLPs, a smaller amount of vRNA was detected in the nuclear fraction of CM2-deficient VLP-infected cells than in that of wild-type VLP-infected cells, suggesting that the uncoating process of the CM2-deficient VLPs in the infected cells did not proceed in an appropriate manner. Taken together, the data obtained in the present study indicate that CM2 has a potential role in the genome packaging and uncoating processes of the virus replication cycle.

摘要

CM2 是丙型流感病毒的第二种膜蛋白。尽管其生化特性、编码策略和作为离子通道的特性已得到广泛研究,但 CM2 在病毒复制周期中的作用仍有待阐明。为了阐明这一作用,本研究生成了 CM2 缺失的丙型流感病毒样颗粒(VLPs),并检测了产生 VLPs 的 293T 细胞、VLPs 和感染的 HMV-II 细胞。通过实时 PCR 对 VLPs 中的病毒 RNA(vRNA)进行定量,结果显示,CM2 缺失的 VLPs 中含有约三分之一的野生型 VLPs 中的 vRNA,尽管在产生 VLPs 的细胞中病毒成分的表达水平或产生的 VLPs 的数量和形态上没有检测到显著差异。这一发现表明 CM2 参与了基因组包装到 VLPs 的过程。此外,感染 CM2 缺失 VLPs 的 HMV-II 细胞表现出明显降低的报告基因表达。尽管 CM2 缺失的 VLPs 能够像野生型 VLPs 一样有效地被内化到 HMV-II 细胞中,但在 CM2 缺失的 VLP 感染细胞的核部分中检测到的 vRNA 量明显少于野生型 VLP 感染细胞,这表明感染细胞中 CM2 缺失的 VLPs 的脱壳过程没有以适当的方式进行。综上所述,本研究获得的数据表明,CM2 在病毒复制周期的基因组包装和脱壳过程中具有潜在作用。