• 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

噬菌体φ29 DNA中富含A-T区域与枯草芽孢杆菌RNA聚合酶结合位点的比较。

Comparison of the A-T rich regions and the Bacillus subtilis RNA polymerase binding sites in phage phi 29 DNA.

作者信息

Sogo J M, Rodeño P, Koller T, Viñuela E, Salas M

出版信息

Nucleic Acids Res. 1979 Sep 11;7(1):107-20. doi: 10.1093/nar/7.1.107.

DOI:10.1093/nar/7.1.107
PMID:114982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC327999/
Abstract

By using a modification of the BAC spreading method for mounting the DNA for electron microscopy, partial denaturation maps of protein-free phi 29 DNA and of phi 29 DNA containing protein p3 were obtained. In phi 29 p3-DNA1 the protein does not seem to influence the melting of the ends of the molecules. The comparison of the partial denaturation map and the B. subtilis RNA polymerase binding sites indicates that five of the seven early promoters (A1, A2, A3, B2 and C2) are located in A-T rich DNA regions whereas the other two early promoters (B1 and C1) are located in less A-T rich sites.

摘要

通过对用于电子显微镜观察的DNA进行安装的BAC铺展方法进行改进,获得了无蛋白质的phi 29 DNA和含有蛋白质p3的phi 29 DNA的部分变性图谱。在phi 29 p3-DNA1中,该蛋白质似乎不影响分子末端的解链。部分变性图谱与枯草芽孢杆菌RNA聚合酶结合位点的比较表明,七个早期启动子中的五个(A1、A2、A3、B2和C2)位于富含A-T的DNA区域,而另外两个早期启动子(B1和C1)位于富含A-T较少的位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df64/327999/716f805e1bc4/nar00454-0119-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df64/327999/2608e76c702e/nar00454-0114-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df64/327999/d5b301e4d95e/nar00454-0116-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df64/327999/716f805e1bc4/nar00454-0119-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df64/327999/2608e76c702e/nar00454-0114-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df64/327999/d5b301e4d95e/nar00454-0116-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df64/327999/716f805e1bc4/nar00454-0119-a.jpg

相似文献

1
Comparison of the A-T rich regions and the Bacillus subtilis RNA polymerase binding sites in phage phi 29 DNA.噬菌体φ29 DNA中富含A-T区域与枯草芽孢杆菌RNA聚合酶结合位点的比较。
Nucleic Acids Res. 1979 Sep 11;7(1):107-20. doi: 10.1093/nar/7.1.107.
2
In vitro transcription of the Bacillus subtilis phage phi 29 DNA by Bacillus subtilis and Escherichia coli RNA polymerases.枯草芽孢杆菌噬菌体phi 29 DNA在枯草芽孢杆菌和大肠杆菌RNA聚合酶作用下的体外转录
Nucleic Acids Res. 1984 Feb 24;12(4):1943-60. doi: 10.1093/nar/12.4.1943.
3
DNA of the Streptomyces phage SH10: binding sites for Escherichia coli RNA polymerase and denaturation map.链霉菌噬菌体SH10的DNA:大肠杆菌RNA聚合酶的结合位点及变性图谱。
Mol Gen Genet. 1983;189(1):21-6. doi: 10.1007/BF00326050.
4
Specificity of promoter site utilization in vitro by bacterial RNA polymerases on Bacillus phage phi 29 DNA. Transcription mapping with exonuclease III.细菌RNA聚合酶在体外对芽孢杆菌噬菌体φ29 DNA上启动子位点利用的特异性。用核酸外切酶III进行转录图谱分析。
J Biol Chem. 1980 Sep 25;255(18):8819-30.
5
Initiation of Bacillus subtilis ribonucleic acid polymerase on deoxyribonucleic acid from bacteriophages 2C, phi 29, T4, and lambda.枯草芽孢杆菌核糖核酸聚合酶在噬菌体2C、phi 29、T4和λ的脱氧核糖核酸上的起始作用。
J Bacteriol. 1972 Jul;111(1):15-23. doi: 10.1128/jb.111.1.15-23.1972.
6
Effect of the delta subunit of Bacillus subtilis RNA polymerase on initiation of RNA synthesis at two bacteriophage phi 29 promoters.枯草芽孢杆菌RNA聚合酶δ亚基对两个噬菌体φ29启动子处RNA合成起始的影响。
Biochemistry. 1987 Dec 15;26(25):8206-13. doi: 10.1021/bi00399a028.
7
RNA polymerase binding sites and transcription map of the DNA of Bacillus subtilis phage phi29.枯草芽孢杆菌噬菌体φ29 DNA的RNA聚合酶结合位点及转录图谱
J Mol Biol. 1979 Feb 5;127(4):411-36. doi: 10.1016/0022-2836(79)90230-4.
8
Bacteriophage SP82 induced modifications of Bacillus subtilis RNA polymerase result in the recognition of additional RNA synthesis initiation sites on phage DNA.噬菌体SP82诱导的枯草芽孢杆菌RNA聚合酶修饰导致在噬菌体DNA上识别出额外的RNA合成起始位点。
Biochem Biophys Res Commun. 1978 Apr 14;81(3):1058-65. doi: 10.1016/0006-291x(78)91458-4.
9
Purification of Bacillus subtilis RNA polymerase with heparin-agarose. In vitro transcription of phi 29 DNA.用肝素琼脂糖纯化枯草芽孢杆菌RNA聚合酶。φ29 DNA的体外转录。
J Biol Chem. 1979 Sep 25;254(18):9220-6.
10
A comparison of the phage T4 gene 32 protein and Escherichia coli RNA polymerase binding sites on hamster papovavirus DNA.
Biochim Biophys Acta. 1982 Jan 26;696(1):102-6. doi: 10.1016/0167-4781(82)90015-x.

引用本文的文献

1
Ribosomal gene clusters are uniquely proportioned between open and closed chromatin structures in both tomato leaf cells and exponentially growing suspension cultures.核糖体基因簇在番茄叶细胞和指数生长的悬浮培养物中的开放和封闭染色质结构之间具有独特的比例。
Proc Natl Acad Sci U S A. 1992 Jun 15;89(12):5256-60. doi: 10.1073/pnas.89.12.5256.
2
Plasmid replication functions. VII. Electron microscopic localization of RNA polymerase binding sites in the replication control region of plasmid R6-5.质粒复制功能。VII. 质粒R6 - 5复制控制区域中RNA聚合酶结合位点的电子显微镜定位
Mol Gen Genet. 1981;183(3):490-6. doi: 10.1007/BF00268770.
3

本文引用的文献

1
A denaturation map of the lambda phage DNA molecule determined by electron microscopy.通过电子显微镜测定的λ噬菌体DNA分子的变性图谱。
J Mol Biol. 1966 Jul;18(3):464-76. doi: 10.1016/s0022-2836(66)80037-2.
2
Electron microscopic study of the ethidium bromide-DNA complex.溴化乙锭 - DNA复合物的电子显微镜研究
J Mol Biol. 1971 Sep 14;60(2):401-3. doi: 10.1016/0022-2836(71)90303-2.
3
Biophysical properties of bacteriophage phi29.噬菌体φ29的生物物理特性
Structure of replicating DNA molecules of Bacillus subtilis bacteriophage phi 29.
枯草芽孢杆菌噬菌体 phi 29 复制性 DNA 分子的结构
J Virol. 1980 Apr;34(1):187-99. doi: 10.1128/JVI.34.1.187-199.1980.
4
DNA of the Streptomyces phage SH10: binding sites for Escherichia coli RNA polymerase and denaturation map.链霉菌噬菌体SH10的DNA:大肠杆菌RNA聚合酶的结合位点及变性图谱。
Mol Gen Genet. 1983;189(1):21-6. doi: 10.1007/BF00326050.
5
In vitro transcription of the Bacillus subtilis phage phi 29 DNA by Bacillus subtilis and Escherichia coli RNA polymerases.枯草芽孢杆菌噬菌体phi 29 DNA在枯草芽孢杆菌和大肠杆菌RNA聚合酶作用下的体外转录
Nucleic Acids Res. 1984 Feb 24;12(4):1943-60. doi: 10.1093/nar/12.4.1943.
6
Structural organization of the two main rDNA size classes of Ascaris lumbricoides.蛔虫两种主要核糖体DNA大小类别的结构组织
Nucleic Acids Res. 1984 Feb 10;12(3):1313-32. doi: 10.1093/nar/12.3.1313.
7
Nucleotide sequence at the termini of the DNA of Bacillus subtilis phage phi 29.枯草芽孢杆菌噬菌体 phi 29 DNA 末端的核苷酸序列。
Proc Natl Acad Sci U S A. 1981 Mar;78(3):1446-50. doi: 10.1073/pnas.78.3.1446.
Virology. 1974 Jan;57(1):112-21. doi: 10.1016/0042-6822(74)90112-3.
4
Temperature-sensitive mutants affected in DNA synthesis in phage phi29 of Bacillus subtilis.枯草芽孢杆菌噬菌体phi29中DNA合成受影响的温度敏感突变体。
Eur J Biochem. 1972 Dec 4;31(2):367-71. doi: 10.1111/j.1432-1033.1972.tb02542.x.
5
An electron microscopic method for studying nucleic acid-protein complexes. Visualization of RNA polymerase bound to the DNA of bacteriophages T7 and T3.一种用于研究核酸 - 蛋白质复合物的电子显微镜方法。可视化与噬菌体T7和T3的DNA结合的RNA聚合酶。
Biopolymers. 1974 May;13(5):995-1009. doi: 10.1002/bip.1974.360130514.
6
Denaturation map of bacteriophage T7 DNA and direction of DNA transcription.噬菌体T7 DNA的变性图谱及DNA转录方向。
J Mol Biol. 1972 Sep 28;70(2):239-51. doi: 10.1016/0022-2836(72)90536-0.
7
Viral protein synthesis in bacteriophage phi 29-infected Bacillus subtilis.噬菌体phi 29感染的枯草芽孢杆菌中的病毒蛋白质合成
J Virol. 1973 Nov;12(5):1149-59. doi: 10.1128/JVI.12.5.1149-1159.1973.
8
Proteins induced in Bacillus subtilis infected with bacteriophage phi 29.在被噬菌体phi 29感染的枯草芽孢杆菌中诱导产生的蛋白质。
Virology. 1973 Nov;56(1):291-9.
9
Thermolabile transfecting DNA from temperature-sensitive mutant of phage phi29.
Nature. 1976;259(5538):60-3. doi: 10.1038/259060a0.
10
Partial denaturation mapping of cloned histone DNA from the sea urchin Psammechinus miliaris.海胆沙钱克隆组蛋白DNA的部分变性图谱分析
Nature. 1976 Nov 4;264(5581):31-4. doi: 10.1038/264031a0.