• 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

反式激活蛋白和顺式作用DNA元件对真核基因表达的调控。

Regulation of eukaryotic gene expression by transactivating proteins and cis acting DNA elements.

作者信息

Yaniv M

出版信息

Biol Cell. 1984;50(3):203-16. doi: 10.1111/j.1768-322x.1984.tb00268.x.

DOI:10.1111/j.1768-322x.1984.tb00268.x
PMID:6235875
Abstract

In this review we try to examine some of the recent developments in our understanding of the mechanisms that control gene expression in eukaryotes. We discuss the nature of the positive regulation exerted by adenovirus, herpes virus or papova immediate early proteins. These proteins which can activate homologous promoters can also stimulate transcription from cellular promoters present on transfected DNA. This property of the E1a gene product of Adenovirus e.g. may be related to its immortalizing function. Transcription of cellular genes can be stimulated by viral or cellular short DNA elements named enhancers. These elements acting in cis, can be placed 5' or 3' to the gene and function in both orientations. Some of them show a remarkable cell specificity in their action. Enhancers affect the chromatin structure by creating a local nuclease sensitive region that may serve as an entry site for RNA polymerase II or for factors involved in the process of transcription initiation.

摘要

在本综述中,我们试图探讨在理解真核生物基因表达调控机制方面的一些最新进展。我们讨论腺病毒、疱疹病毒或乳头瘤病毒立即早期蛋白所施加的正调控的性质。这些能够激活同源启动子的蛋白,也能刺激转染DNA上存在的细胞启动子的转录。例如,腺病毒E1a基因产物的这一特性可能与其永生化功能有关。细胞基因的转录可被称为增强子的病毒或细胞短DNA元件所刺激。这些顺式作用元件可置于基因的5'端或3'端,并以两种方向发挥作用。其中一些在作用上表现出显著的细胞特异性。增强子通过创建一个局部核酸酶敏感区域来影响染色质结构,该区域可能作为RNA聚合酶II或转录起始过程中涉及的因子的进入位点。

相似文献

1
Regulation of eukaryotic gene expression by transactivating proteins and cis acting DNA elements.反式激活蛋白和顺式作用DNA元件对真核基因表达的调控。
Biol Cell. 1984;50(3):203-16. doi: 10.1111/j.1768-322x.1984.tb00268.x.
2
Local stability involved in characterizing and controlling promoters in eukaryotes.
Folia Biol (Praha). 1984;30 Spec No:93-104.
3
Adenovirus early region 1A protein activates transcription of a nonviral gene introduced into mammalian cells by infection or transfection.腺病毒早期区域1A蛋白可激活通过感染或转染导入哺乳动物细胞的非病毒基因的转录。
Proc Natl Acad Sci U S A. 1984 Feb;81(4):1193-7. doi: 10.1073/pnas.81.4.1193.
4
Activation of gene expression by adenovirus and herpesvirus regulatory genes acting in trans and by a cis-acting adenovirus enhancer element.腺病毒和疱疹病毒的反式作用调控基因以及顺式作用的腺病毒增强子元件对基因表达的激活作用。
Cell. 1983 Nov;35(1):127-36. doi: 10.1016/0092-8674(83)90215-5.
5
Multiple cis-acting DNA elements that regulate transcription of the adenovirus 12 E1A gene.
Virus Genes. 1992 Aug;6(3):261-71. doi: 10.1007/BF01702564.
6
Trans activation of plasmid-borne promoters by adenovirus and several herpes group viruses.腺病毒和几种疱疹病毒科病毒对质粒携带启动子的反式激活作用。
Nucleic Acids Res. 1984 Aug 10;12(15):5969-78. doi: 10.1093/nar/12.15.5969.
7
Expression of the chloramphenicol acetyltransferase gene in mammalian cells under the control of adenovirus type 12 promoters: effect of promoter methylation on gene expression.氯霉素乙酰转移酶基因在12型腺病毒启动子控制下在哺乳动物细胞中的表达:启动子甲基化对基因表达的影响。
Proc Natl Acad Sci U S A. 1983 Dec;80(24):7586-90. doi: 10.1073/pnas.80.24.7586.
8
Cis and trans activation of adenovirus IVa2 gene transcription.腺病毒IVa2基因转录的顺式和反式激活
Nucleic Acids Res. 1985 Jun 11;13(11):4067-83. doi: 10.1093/nar/13.11.4067.
9
A detailed analysis of an HSV-1 early promoter: sequences involved in trans-activation by viral immediate-early gene products are not early-gene specific.对单纯疱疹病毒1型早期启动子的详细分析:病毒立即早期基因产物参与反式激活的序列并非早期基因特异性的。
Nucleic Acids Res. 1984 Apr 11;12(7):3037-56. doi: 10.1093/nar/12.7.3037.
10
Functional relation between HTLV-II x and adenovirus E1A proteins in transcriptional activation.
Science. 1985 Nov 1;230(4725):570-3. doi: 10.1126/science.2996140.

引用本文的文献

1
From adjacent activation in Escherichia coli and DNA cyclization to eukaryotic enhancers: the elements of a puzzle.从大肠杆菌中的相邻激活和DNA环化到真核生物增强子:谜题的要素
Front Genet. 2014 Nov 3;5:371. doi: 10.3389/fgene.2014.00371. eCollection 2014.
2
An autonomous DNA nanomachine maps spatiotemporal pH changes in a multicellular living organism.一种自主 DNA 纳米机器绘制出多细胞生物体内时空 pH 变化。
Nat Commun. 2011 Jun 7;2:340. doi: 10.1038/ncomms1340.
3
In vivo interactions of the Acanthamoeba TBP gene promoter.棘阿米巴TBP基因启动子的体内相互作用。
Nucleic Acids Res. 2004 Feb 19;32(4):1251-60. doi: 10.1093/nar/gkh297. Print 2004.
4
A 5'-flanking region of the chicken acetylcholine receptor alpha-subunit gene confers tissue specificity and developmental control of expression in transfected cells.鸡乙酰胆碱受体α亚基基因的5'侧翼区域赋予转染细胞中表达的组织特异性和发育调控。
Mol Cell Biol. 1987 Feb;7(2):951-5. doi: 10.1128/mcb.7.2.951-955.1987.
5
Compilation and analysis of eukaryotic POL II promoter sequences.真核生物RNA聚合酶II启动子序列的汇编与分析
Nucleic Acids Res. 1986 Dec 22;14(24):10009-26. doi: 10.1093/nar/14.24.10009.
6
The 5' region of the human transferrin gene: structure and potential regulatory sites.人类转铁蛋白基因的5'区域:结构与潜在调控位点
Nucleic Acids Res. 1986 Nov 11;14(21):8692. doi: 10.1093/nar/14.21.8692.
7
An RNA polymerase I enhancer in Saccharomyces cerevisiae.酿酒酵母中的一种RNA聚合酶I增强子。
Mol Cell Biol. 1986 Jun;6(6):2089-97. doi: 10.1128/mcb.6.6.2089-2097.1986.
8
Analysis of the tissue-specific enhancer at the 3' end of the chicken adult beta-globin gene.鸡成年β-珠蛋白基因3'端组织特异性增强子的分析。
Proc Natl Acad Sci U S A. 1987 Jul;84(14):4786-90. doi: 10.1073/pnas.84.14.4786.
9
Organisation of the entire rabbit progesterone receptor mRNA and of the promoter and 5' flanking region of the gene.
Nucleic Acids Res. 1988 Jun 24;16(12):5459-72. doi: 10.1093/nar/16.12.5459.
10
Essential and nonessential sequences in malPp, a positively controlled promoter in Escherichia coli.malPp(大肠杆菌中一个正调控启动子)中的必需序列和非必需序列。
J Bacteriol. 1985 Mar;161(3):1201-8. doi: 10.1128/jb.161.3.1201-1208.1985.