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Nonstructural protein of parvoviruses B19 and minute virus of mice controls transcription.

作者信息

Doerig C, Hirt B, Antonietti J P, Beard P

机构信息

Department of Virology, Swiss Institute for Experimental Cancer Research, Epalinges.

出版信息

J Virol. 1990 Jan;64(1):387-96. doi: 10.1128/JVI.64.1.387-396.1990.

DOI:10.1128/JVI.64.1.387-396.1990
PMID:2293668
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC249113/
Abstract

The genome of the human parvovirus B19 contains a transcriptional promoter (BP06) at map position 6, upstream from the nonstructural protein genes. By cotransfecting HeLa cells with this promoter cloned before the chloramphenicol acetyltransferase (CAT) gene together with a plasmid containing almost the whole B19 genome, we showed that BP06 is transactivated by a B19 gene product. The transactivating viral protein was identified as the nonstructural protein NS-1. NS-1 synthesized in a wheat germ extract specifically stimulates transcription from BP06 in vitro. NS-1 of the minute virus of mice (MVM) activates the analogous MVM promoter, MP04. NS-1, therefore, has a positive feedback effect on the activity of its own promoter. Moreover, NS-1 of MVM activates the human BP06. We have identified, in the genome of B19, a second transcriptional promoter activity at map position 44, before the capsid protein genes. This promoter, BP44, was identified by cloning fragments of B19 DNA upstream of the CAT gene, transfecting the DNA into HeLa cells, and measuring CAT expression. The strength of the BP44 promoter is similar to that of the capsid gene promoter, MP39, of MVM. In (nonpermissive) HeLa cells, the BP44 promoter is not activated by NS-1. Thus, the BP06 promoter apparently does not determine the tissue specificity of B19 virus but BP44 could do so.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad3c/249113/84f2280e4180/jvirol00056-0409-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad3c/249113/908e0f186caa/jvirol00056-0406-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad3c/249113/2cb3f16f7d8c/jvirol00056-0407-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad3c/249113/2bc46ad09b9b/jvirol00056-0408-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad3c/249113/65d72359db3b/jvirol00056-0409-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad3c/249113/84f2280e4180/jvirol00056-0409-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad3c/249113/908e0f186caa/jvirol00056-0406-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad3c/249113/2cb3f16f7d8c/jvirol00056-0407-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad3c/249113/2bc46ad09b9b/jvirol00056-0408-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad3c/249113/65d72359db3b/jvirol00056-0409-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad3c/249113/84f2280e4180/jvirol00056-0409-b.jpg

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在卡塔尔居住的不同国籍献血者中细小病毒(B19V)的流行情况及系统进化分析。
Viruses. 2021 Mar 24;13(4):540. doi: 10.3390/v13040540.
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The VP1u of Human Parvovirus B19: A Multifunctional Capsid Protein with Biotechnological Applications.人细小病毒 B19 的 VP1u:一种具有生物技术应用的多功能衣壳蛋白。
Viruses. 2020 Dec 18;12(12):1463. doi: 10.3390/v12121463.
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Generation and molecular characteristics of a highly attenuated GPV strain through adaptation in GEF cells.通过在 GEF 细胞中的适应,产生并鉴定了一种高度减毒的 GPV 株及其分子特征。
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The human parvovirus B19 non-structural protein 1 N-terminal domain specifically binds to the origin of replication in the viral DNA.人细小病毒 B19 非结构蛋白 1 N 端结构域特异性结合到病毒 DNA 复制起点。
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