• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Expression of the non-structural proteins of parvovirus MVMp from recombinant retroviruses: predominant role of the parvoviral NS-1 product in host cell disturbance.

作者信息

Becquart P, Vanacker J M, Duponchel N, Bègue A, Rommelaere J

机构信息

Institut Pasteur de Lille, Molecular Oncology Unit, France.

出版信息

Res Virol. 1993 Nov-Dec;144(6):465-70. doi: 10.1016/s0923-2516(06)80061-0.

DOI:10.1016/s0923-2516(06)80061-0
PMID:8140289
Abstract

Stable Psi-2 cell transformants were selected for their resistance to neomycin after transfection with a retroviral pZipNeo-SVX vector carrying sequences encoding for the non-structural proteins of parvovirus minute virus of mice (prototype strain, MVMp). Cells producing both NS-1 and NS-2 proteins (PsiNS) or only the NS-2 polypeptide (PsiNS2) were obtained. PsiNS cells exhibited morphological abnormalities and had a reduced clone-forming ability, whereas PsiNS2 cells were indistinguishable from the parental line. These cellular systems produced recombinant retroviral particles which transduced the NS gene(s) into mouse A9 cells. As in the case of Psi-2 cells, A9 transformants expressing both NS-1 and NS-2 proteins were impaired in their cloning efficiency. These results provided a direct confirmation of the predominant role of protein NS-1 in the cytopathic effect of parvoviruses.

摘要

相似文献

1
Expression of the non-structural proteins of parvovirus MVMp from recombinant retroviruses: predominant role of the parvoviral NS-1 product in host cell disturbance.
Res Virol. 1993 Nov-Dec;144(6):465-70. doi: 10.1016/s0923-2516(06)80061-0.
2
NS-1 and NS-2 proteins may act synergistically in the cytopathogenicity of parvovirus MVMp.NS-1和NS-2蛋白可能在细小病毒MVMp的细胞致病性中协同发挥作用。
Virology. 1990 Feb;174(2):576-84. doi: 10.1016/0042-6822(90)90110-d.
3
Activation of promoter P4 of the autonomous parvovirus minute virus of mice at early S phase is required for productive infection.在S期早期激活自主细小病毒小鼠微小病毒的启动子P4是产生性感染所必需的。
J Virol. 1999 May;73(5):3877-85. doi: 10.1128/JVI.73.5.3877-3885.1999.
4
The cytotoxicity of the autonomous parvovirus minute virus of mice nonstructural proteins in FR3T3 rat cells depends on oncogene expression.小鼠自主细小病毒非结构蛋白在FR3T3大鼠细胞中的细胞毒性取决于癌基因表达。
J Virol. 1994 Oct;68(10):6446-53. doi: 10.1128/JVI.68.10.6446-6453.1994.
5
Targeting of promoters for trans activation by a carboxy-terminal domain of the NS-1 protein of the parvovirus minute virus of mice.通过小鼠细小病毒NS-1蛋白的羧基末端结构域对启动子进行反式激活的靶向作用。
J Virol. 1994 Dec;68(12):7974-85. doi: 10.1128/JVI.68.12.7974-7985.1994.
6
Genome replication and postencapsidation functions mapping to the nonstructural gene restrict the host range of a murine parvovirus in human cells.定位于非结构基因的基因组复制和衣壳化后功能限制了鼠细小病毒在人细胞中的宿主范围。
J Virol. 2001 Dec;75(23):11573-82. doi: 10.1128/JVI.75.23.11573-11582.2001.
7
Transcriptional inhibition of the parvovirus minute virus of mice by constitutive expression of an antisense RNA targeted against the NS-1 transactivator protein.
Virology. 1995 Jan 10;206(1):57-68. doi: 10.1016/s0042-6822(95)80019-0.
8
Induced expression of the conditionally cytotoxic herpes simplex virus thymidine kinase gene by means of a parvoviral regulatory circuit.
Hum Gene Ther. 1994 Apr;5(4):457-63. doi: 10.1089/hum.1994.5.4-457.
9
Inhibition of heterologous DNA replication by the MVMp nonstructural NS-1 protein: identification of a target sequence.
Virology. 1993 Dec;197(2):630-41. doi: 10.1006/viro.1993.1638.
10
Protein species of the parvovirus minute virus of mice strain MVMp: involvement of phosphorylated VP-2 subtypes in viral morphogenesis.小鼠细小病毒MVMp株的蛋白质种类:磷酸化VP - 2亚型在病毒形态发生中的作用
J Virol. 1993 Sep;67(9):5126-38. doi: 10.1128/JVI.67.9.5126-5138.1993.