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在细小病毒科中鉴定到的新型人细小病毒 4 的分子特征。

Molecular characterization of the newly identified human parvovirus 4 in the family Parvoviridae.

机构信息

Department of Infectious Diseases, First Affiliated Hospital, School of Medicine, Xi'an Jiaotong University, Xi'an, China.

出版信息

Virology. 2012 Jan 5;422(1):59-69. doi: 10.1016/j.virol.2011.09.033. Epub 2011 Oct 30.

Abstract

Human parvovirus 4 (PARV4) is an emerging human virus, and little is known about the molecular aspects of PARV4 apart from its incomplete genome sequence, which lacks information of the termini. We analyzed the gene expression profile of PARV4 using a nearly full-length HPV4 genome in a replication competent system in 293 cells. We found that PARV4 utilizes two promoters to transcribe non-structural protein- and structural protein-encoding mRNAs, respectively, which were polyadenylated at the right end of the genome. Three major proteins, including the large non-structural protein NS1a, whose mRNA is spliced, and capsid proteins VP1 and VP2, were detected. Additional functional analysis of the NS1a revealed its capability to induce cell cycle arrest at G2/M phase in ex vivo-generated human hematopoietic stem cells. Taken together, our characterization of the molecular features of PARV4 suggests that PARV4 represents a new genus in the family Parvoviridae.

摘要

人细小病毒 4 型(PARV4)是一种新兴的人类病毒,除了其不完整的基因组序列外,人们对 PARV4 的分子方面知之甚少,该序列缺少末端信息。我们在 293 细胞中使用具有复制能力的系统,对近乎全长的 HPV4 基因组进行分析,以研究 PARV4 的基因表达谱。我们发现 PARV4 利用两个启动子分别转录非结构蛋白编码和结构蛋白编码的 mRNA,这些 mRNA 在基因组的右端聚腺苷酸化。检测到三种主要蛋白,包括经剪接的大非结构蛋白 NS1a,以及衣壳蛋白 VP1 和 VP2。对 NS1a 的进一步功能分析表明,它能够诱导体外生成的人类造血干细胞停滞在 G2/M 期。总之,我们对 PARV4 分子特征的描述表明,PARV4 代表细小病毒科中的一个新属。

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