• 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

Functional analysis of human cytomegalovirus morphological transforming region II (mtrII).

作者信息

Razzaque A, Zhu F, Jones C

机构信息

Division of Virology, CBER, FDA, Bethesda, Maryland 20892.

出版信息

Virology. 1991 Mar;181(1):399-402. doi: 10.1016/0042-6822(91)90513-b.

DOI:10.1016/0042-6822(91)90513-b
PMID:1847262
Abstract

Human cytomegalovirus (HCMV) transforming region II (mtrII), a 980-bp sequence, can transform rodent fibroblasts. This region contains three small potential open reading frames (ORFs) of 79, 83, and 34 amino acid residues. To identify the specific role of mtrII sequences in transformation, we investigated (1) the presence of mtrII DNA and mtrII-specific RNA transcripts in NIH 3T3 transformants and their tumor derivatives, and (2) the ability of mtrII DNA and its subregions to cis-activate chloramphenicol acetyl transferase (CAT) gene expression. By hybridization analysis, mtrII-specific DNA and RNA were detected in both transformed and tumor cells. A 285-bp sequence upstream of the ORFs in mtrII exhibited weak promoter activity when linked to CAT gene in the sense orientation with respect to the ORFs. Promoter activity of this region was stronger than the enhancer activity in the sense orientation. No promoter or enhancer activity was detected in the antisense orientation. The mtrII 980-bp sequence did not exhibit any promoter activity in either orientation. These results suggested that HCMV mtrII may contain a small transforming gene that may be transcribed at low levels from its own promoter.

摘要

相似文献

1
Functional analysis of human cytomegalovirus morphological transforming region II (mtrII).
Virology. 1991 Mar;181(1):399-402. doi: 10.1016/0042-6822(91)90513-b.
2
Identification of two promoters within human cytomegalovirus morphologic transforming region II.人巨细胞病毒形态转化区域II内两个启动子的鉴定
Intervirology. 1992;34(3):146-53. doi: 10.1159/000150275.
3
The human cytomegalovirus mtrII colinear region in strain Tanaka is transformation defective.田中型人巨细胞病毒mtrII共线性区域存在转化缺陷。
J Virol. 1989 Jun;63(6):2866-9. doi: 10.1128/JVI.63.6.2866-2869.1989.
4
Localization and DNA sequence analysis of the transforming domain (mtrII) of human cytomegalovirus.人巨细胞病毒转化结构域(mtrII)的定位与DNA序列分析
Proc Natl Acad Sci U S A. 1988 Aug;85(15):5709-13. doi: 10.1073/pnas.85.15.5709.
5
A 79 amino acid oncogene is responsible for human cytomegalovirus mtrII induced malignant transformation.一种79个氨基酸的致癌基因导致人巨细胞病毒mtrII诱导的恶性转化。
Arch Virol. 1994;136(1-2):161-72. doi: 10.1007/BF01538825.
6
Human cytomegalovirus mtrII oncoprotein binds to p53 and down-regulates p53-activated transcription.人巨细胞病毒mtrII癌蛋白与p53结合并下调p53激活的转录。
J Virol. 1996 Dec;70(12):8691-700. doi: 10.1128/JVI.70.12.8691-8700.1996.
7
Human cytomegalovirus and human herpesvirus 6 genes that transform and transactivate.具有转化和反式激活功能的人巨细胞病毒和人疱疹病毒6基因。
Clin Microbiol Rev. 1999 Jul;12(3):367-82. doi: 10.1128/CMR.12.3.367.
8
Differences in retention and expression of transfected human cytomegalovirus Towne XbaI-E transforming fragment in human cervical and NIH 3T3 lines.转染的人巨细胞病毒Towne XbaI-E转化片段在人宫颈细胞系和NIH 3T3细胞系中的保留及表达差异。
Intervirology. 1992;33(4):187-96. doi: 10.1159/000150250.
9
Mapping and DNA sequence analysis of the cytomegalovirus transforming domain III (mtrIII).巨细胞病毒转化结构域III(mtrIII)的图谱绘制与DNA序列分析
Virus Res. 1993 Dec;30(3):221-38. doi: 10.1016/0168-1702(93)90092-2.
10
The promoter-regulatory region of the major immediate-early gene of human cytomegalovirus responds to T-lymphocyte stimulation and contains functional cyclic AMP-response elements.人巨细胞病毒主要立即早期基因的启动子调控区域对T淋巴细胞刺激有反应,并含有功能性环磷酸腺苷反应元件。
J Virol. 1989 Jul;63(7):3026-33. doi: 10.1128/JVI.63.7.3026-3033.1989.

引用本文的文献

1
The emerging role of human cytomegalovirus infection in human carcinogenesis: a review of current evidence and potential therapeutic implications.人巨细胞病毒感染在人类致癌过程中的新作用:当前证据及潜在治疗意义综述
Oncotarget. 2019 Jul 2;10(42):4333-4347. doi: 10.18632/oncotarget.27016.
2
Cytomegalovirus in human brain tumors: Role in pathogenesis and potential treatment options.人脑肿瘤中的巨细胞病毒:在发病机制中的作用及潜在治疗选择
World J Exp Med. 2015 Feb 20;5(1):1-10. doi: 10.5493/wjem.v5.i1.1.
3
Identification of novel viral interleukin-10 isoforms of human cytomegalovirus AD169.
人巨细胞病毒AD169新型病毒白细胞介素-10亚型的鉴定
Virus Res. 2008 Feb;131(2):213-23. doi: 10.1016/j.virusres.2007.09.011. Epub 2007 Nov 5.
4
Human cytomegalovirus and human herpesvirus 6 genes that transform and transactivate.具有转化和反式激活功能的人巨细胞病毒和人疱疹病毒6基因。
Clin Microbiol Rev. 1999 Jul;12(3):367-82. doi: 10.1128/CMR.12.3.367.
5
Human cytomagalovirus IE1 and IE2 proteins are mutagenic and mediate "hit-and-run" oncogenic transformation in cooperation with the adenovirus E1A proteins.人巨细胞病毒IE1和IE2蛋白具有致突变性,并与腺病毒E1A蛋白协同介导“打了就跑”的致癌转化。
Proc Natl Acad Sci U S A. 1997 Apr 1;94(7):3341-5. doi: 10.1073/pnas.94.7.3341.
6
Congenital infection by human cytomegalovirus with a 65bp deletion in the morphological transforming region II.
Arch Virol. 1993;129(1-4):295-9. doi: 10.1007/BF01316904.