• 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

大肠杆菌RNA聚合酶结合位点在噬菌体S13和phiX174 DNA上的定位:与限制性内切酶图谱的比对

Localization of Escherichia coli RNA polymerase binding sites on bacteriophage S13 and phiX174 DNA: alignment with restriction enzyme maps.

作者信息

Rassart E, Spencer J H

出版信息

J Virol. 1978 Sep;27(3):677-87. doi: 10.1128/JVI.27.3.677-687.1978.

DOI:10.1128/JVI.27.3.677-687.1978
PMID:359830
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC525856/
Abstract

Escherichia coli RNA polymerase has been shown to bind to a limited number of Hind and Hae III restriction enzyme fragments. On S13 replicative form DNA there are three major binding sites, and the locations correlate with promoter sites at the beginning of genes a and B and a site overlapping gene D and the beginning of gene E. Two less definite binding sites have been localized, one in gene F and one at the gene G-H junction. In phiX174 replicative form DNA, five sites, each with apparently similar binding properties, have been located, four of which correspond exactly to binding sites in S13. One site, at the beginning of the B gene, could not be assigned to exactly the same location found in S13. This was due in part to differences in the restriction cleavage maps in the area of the DNA and possibly to the higher background of nonspecific binding in the phiX174 experiments. The location of two of the phiX174 sites at the beginning of genes A and D-E corresponds very well with transcription data, but the site at the start of the B gene indicates the promoter site is closer to the initiation sequence of the B protein than was previously suggested on the basis of transcription data.

摘要

已证明大肠杆菌RNA聚合酶可与有限数量的Hind和Hae III限制性酶切片段结合。在S13复制型DNA上有三个主要结合位点,其位置与基因a和B起始处的启动子位点以及与基因D重叠和基因E起始处的一个位点相关。已定位了两个不太明确的结合位点,一个在基因F中,一个在基因G - H交界处。在φX174复制型DNA中,已定位了五个位点,每个位点的结合特性显然相似,其中四个与S13中的结合位点完全对应。在B基因起始处的一个位点,无法确定其与在S13中发现的位置完全相同。这部分是由于DNA区域内限制性酶切图谱的差异,也可能是由于φX174实验中非特异性结合的背景较高。φX174中位于基因A和D - E起始处的两个位点的位置与转录数据非常吻合,但B基因起始处的位点表明启动子位点比根据转录数据先前推测的更接近B蛋白的起始序列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e81/525856/48da89e39959/jvirol00201-0234-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e81/525856/cee6b5d6e061/jvirol00201-0233-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e81/525856/48da89e39959/jvirol00201-0234-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e81/525856/cee6b5d6e061/jvirol00201-0233-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e81/525856/48da89e39959/jvirol00201-0234-a.jpg

相似文献

1
Localization of Escherichia coli RNA polymerase binding sites on bacteriophage S13 and phiX174 DNA: alignment with restriction enzyme maps.大肠杆菌RNA聚合酶结合位点在噬菌体S13和phiX174 DNA上的定位:与限制性内切酶图谱的比对
J Virol. 1978 Sep;27(3):677-87. doi: 10.1128/JVI.27.3.677-687.1978.
2
Localization of Escherichia coli RNA polymerase binding sites on bacteriophage S13 and 0X174 DNAs by electron microscopy.通过电子显微镜对大肠杆菌RNA聚合酶结合位点在噬菌体S13和0X174 DNA上的定位
J Virol. 1979 Jan;29(1):179-84. doi: 10.1128/JVI.29.1.179-184.1979.
3
Localization of Escherichia coli RNA polymerase-binding sites on bacteriophage S13 replicative form I DNA by protection of restriction enzyme cleavage sites.通过限制酶切位点保护法对噬菌体S13复制型I DNA上大肠杆菌RNA聚合酶结合位点的定位
J Virol. 1987 Jul;61(7):2297-303. doi: 10.1128/JVI.61.7.2297-2303.1987.
4
Mapping the initiation sites of in vitro transcripts of bacteriophage S13.绘制噬菌体S13体外转录物的起始位点图谱。
Biochim Biophys Acta. 1994 Aug 2;1218(3):331-8. doi: 10.1016/0167-4781(94)90185-6.
5
Mapping of RNA polymerase binding sites in the H/A gene region of bacteriophage S13 by footprinting and exonuclease III analysis.通过足迹法和核酸外切酶III分析对噬菌体S13的H/A基因区域中的RNA聚合酶结合位点进行定位。
Biochim Biophys Acta. 1994 Aug 2;1218(3):339-45. doi: 10.1016/0167-4781(94)90186-4.
6
[Protection of segments of replicative form I of phiX174 phage DNA recognized by HindII, BspRI, and AluI restrictases by Escherichia coli RNA-polymerase].[大肠杆菌RNA聚合酶对被HindII、BspRI和AluI限制性内切酶识别的φX174噬菌体DNA复制型I片段的保护作用]
Mol Biol (Mosk). 1981 Sep-Oct;15(5):1144-57.
7
Mapping the B and D gene promoters of bacteriophage S13 by footprinting and exonuclease III analysis.通过足迹法和核酸外切酶III分析对噬菌体S13的B和D基因启动子进行定位。
J Virol. 1987 Dec;61(12):3694-700. doi: 10.1128/JVI.61.12.3694-3700.1987.
8
Localization of RNA polymerase binding sites on T7 DNA.T7 DNA上RNA聚合酶结合位点的定位
Virology. 1976 May;71(1):278-90. doi: 10.1016/0042-6822(76)90112-4.
9
Physicochomecial studies on interactions between DNA and RNA polymerase. Isolation and mapping of a T7 DNA fragment containing the early promoters for Escherichia coli RNA polymerase.DNA与RNA聚合酶相互作用的物理化学研究。含有大肠杆菌RNA聚合酶早期启动子的T7 DNA片段的分离与图谱绘制。
Biochemistry. 1976 Dec 28;15(26):5776-83. doi: 10.1021/bi00671a014.
10
Distribution of RNA polymerase binding sites on the P4 chromosome.
Virology. 1979 Jul 15;96(1):274-6. doi: 10.1016/0042-6822(79)90192-2.

引用本文的文献

1
Mechanistic aspects of promoter binding and chain initiation by RNA polymerase.RNA聚合酶与启动子结合及链起始的机制方面。
Mol Cell Biochem. 1982 Sep 17;47(3):129-49. doi: 10.1007/BF00229597.
2
Localization of Escherichia coli RNA polymerase-binding sites on bacteriophage S13 replicative form I DNA by protection of restriction enzyme cleavage sites.通过限制酶切位点保护法对噬菌体S13复制型I DNA上大肠杆菌RNA聚合酶结合位点的定位
J Virol. 1987 Jul;61(7):2297-303. doi: 10.1128/JVI.61.7.2297-2303.1987.
3
Mapping the B and D gene promoters of bacteriophage S13 by footprinting and exonuclease III analysis.

本文引用的文献

1
Studies on the binding of RNA polymerase to polynucleotides.RNA聚合酶与多核苷酸结合的研究。
J Mol Biol. 1966 Dec 28;22(2):199-209. doi: 10.1016/0022-2836(66)90126-4.
2
Mutagenic methods for determining which DNA strand is transcribed for individual viral genes.用于确定单个病毒基因转录的是哪条DNA链的诱变方法。
Nature. 1970 Oct 3;228(5266):54-6. doi: 10.1038/228054a0.
3
The binding of RNA polymerase to DNA.RNA聚合酶与DNA的结合。
通过足迹法和核酸外切酶III分析对噬菌体S13的B和D基因启动子进行定位。
J Virol. 1987 Dec;61(12):3694-700. doi: 10.1128/JVI.61.12.3694-3700.1987.
4
Localization of Escherichia coli RNA polymerase binding sites on bacteriophage S13 and 0X174 DNAs by electron microscopy.通过电子显微镜对大肠杆菌RNA聚合酶结合位点在噬菌体S13和0X174 DNA上的定位
J Virol. 1979 Jan;29(1):179-84. doi: 10.1128/JVI.29.1.179-184.1979.
J Mol Biol. 1966 Oct 28;21(1):83-114. doi: 10.1016/0022-2836(66)90081-7.
4
Early replicative form DNA of bacteriophage S13. I. Sucrose gradient analysis of replicative form made by gene IV mutants.噬菌体S13的早期复制型DNA。I. 基因IV突变体产生的复制型的蔗糖梯度分析
J Mol Biol. 1968 May 28;34(1):121-9. doi: 10.1016/0022-2836(68)90238-6.
5
The mechanism of replication of phi X174 single-stranded DNA. 3. An enzymic study of the structure of the replicative form II DNA.φX174单链DNA的复制机制。3. 复制型II DNA结构的酶学研究。
J Mol Biol. 1971 Apr 28;57(2):177-99. doi: 10.1016/0022-2836(71)90340-8.
6
Synthesis of replicative form deoxyribonucleic acid and messenger ribonucleic acid by gene IV mutants of bacteriophage S13.噬菌体S13基因IV突变体对复制型脱氧核糖核酸和信使核糖核酸的合成
J Virol. 1969 Oct;4(4):394-9. doi: 10.1128/JVI.4.4.394-399.1969.
7
Studies of ribonucleic acid chain initiation by Escherichia coli ribonucleic acid polymerase bound to T7 deoxyribonucleic acid. II. The effect of alterations in ionic strength of chain initiation and on the conformation of binary complexes.大肠杆菌核糖核酸聚合酶与T7脱氧核糖核酸结合时核糖核酸链起始的研究。II. 离子强度变化对链起始及二元复合物构象的影响。
J Biol Chem. 1974 May 25;249(10):3002-6.
8
Isolation and genetic localization of three phi-X174 promoter regions.三种噬菌体X174启动子区域的分离与基因定位
Nat New Biol. 1973 Jun 20;243(129):233-6. doi: 10.1038/newbio243233a0.
9
Mechanism of transcription of bacteriophage S13. I. Dependence of messengerRNA synthesis on amount and configuration of DNA.噬菌体S13的转录机制。I. 信使核糖核酸合成对DNA数量和构型的依赖性。
J Mol Biol. 1973 Mar 25;75(1):83-97. doi: 10.1016/0022-2836(73)90530-5.
10
A promoter site and polarity gradients in phage S13.噬菌体S13中的启动子位点和极性梯度。
Virology. 1972 Oct;50(1):171-9. doi: 10.1016/0042-6822(72)90357-1.