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1
Evidence for the presence of nontranslated T7 late mRNA in infected F'(PIF+) episome-containing cells.在感染了含有F'(PIF+)附加体的细胞中存在非翻译T7晚期mRNA的证据。
J Virol. 1974 Feb;13(2):378-85. doi: 10.1128/JVI.13.2.378-385.1974.
2
T7 protein synthesis in F' episome-containing cells: assignment of specific proteins to three translational groups.含有F'附加体的细胞中T7蛋白质合成:特定蛋白质归属于三个翻译组
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3
F-Factor-mediated restriction of bacteriophage T7: protein synthesis in cell-free systems from T7-infected Escherichia coli F- and F+ cells.F因子介导的噬菌体T7限制作用:来自T7感染的大肠杆菌F-和F+细胞的无细胞系统中的蛋白质合成
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4
T7 protein synthesis in F-factor-containing cells: evidence for an episomally induced impairment of translation and relation to an alteration in membrane permeability.含有F因子的细胞中T7蛋白质合成:附加体诱导的翻译损伤证据及其与膜通透性改变的关系。
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5
F-Factor-mediated restriction of bacteriophage T7: synthesis of RNA and protein in T7-infected Escherichia coli F- and F+ cells.F因子介导的噬菌体T7限制作用:T7感染的大肠杆菌F-和F+细胞中RNA和蛋白质的合成
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6
Effect of RNase III on efficiency of translation of bacteriophage T7 lysozyme mRNA.核糖核酸酶III对噬菌体T7溶菌酶信使核糖核酸翻译效率的影响。
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Phage T7 lysozyme mRNA transcription and translation in vivo and in vitro.噬菌体T7溶菌酶mRNA在体内和体外的转录与翻译。
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Macromolecular synthesis in T7 infected F' cells.T7感染的F'细胞中的大分子合成
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[In vivo and in vitro studies of phage T4 lysozyme mRNA translation].[噬菌体T4溶菌酶mRNA翻译的体内和体外研究]
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Defective lysis of streptomycin-resistant escherichia coli cells infected with bacteriophage f2.用噬菌体f2感染的抗链霉素大肠杆菌细胞的裂解缺陷。
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3
Physiological properties of a T7-T3 recombinant bacteriophage that productively infects strains of Escherichia coli that harbor the F plasmid.一种能有效感染携带F质粒的大肠杆菌菌株的T7-T3重组噬菌体的生理特性。
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Cloning of the pif region of the F sex factor and identification of a pif protein product.F 性因子 pif 区域的克隆及一种 pif 蛋白产物的鉴定。
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6
T7 protein synthesis in F' episome-containing cells: assignment of specific proteins to three translational groups.含有F'附加体的细胞中T7蛋白质合成:特定蛋白质归属于三个翻译组
J Virol. 1974 Feb;13(2):386-93. doi: 10.1128/JVI.13.2.386-393.1974.
7
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8
Defective transcription of the right end of bacteriophage T7 DNA during an abortive infection of F plasmid-containing Escherichia coli.在含F质粒的大肠杆菌的流产感染过程中噬菌体T7 DNA右端的转录缺陷。
J Bacteriol. 1991 Feb;173(3):947-54. doi: 10.1128/jb.173.3.947-954.1991.
9
T7 protein synthesis in F-factor-containing cells: evidence for an episomally induced impairment of translation and relation to an alteration in membrane permeability.含有F因子的细胞中T7蛋白质合成:附加体诱导的翻译损伤证据及其与膜通透性改变的关系。
J Virol. 1975 Jan;17(1):94-105. doi: 10.1128/JVI.17.1.94-105.1976.
10
Chemical stability of bacteriophage T7 early mRNA.噬菌体T7早期信使核糖核酸的化学稳定性
J Virol. 1975 Dec;16(6):1683-7. doi: 10.1128/JVI.16.6.1683-1687.1975.

本文引用的文献

1
The dependence of cell-free protein synthesis in E. coli upon naturally occurring or synthetic polyribonucleotides.大肠杆菌中无细胞蛋白质合成对天然存在或合成的多聚核糖核苷酸的依赖性。
Proc Natl Acad Sci U S A. 1961 Oct 15;47(10):1588-602. doi: 10.1073/pnas.47.10.1588.
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SEX-SPECIFICITY OF THE BACTERIOPHAGE T7.噬菌体T7的性别特异性
Ann Med Exp Biol Fenn. 1964;42:188-95.
3
Demonstration of the messenger role of viral RNA.病毒RNA信使作用的证明。
Proc Natl Acad Sci U S A. 1962 May 15;48(5):846-53. doi: 10.1073/pnas.48.5.846.
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Stability of phage T7 gene I mRNA in E. coli cells infected with wild type phage and with gene I amber mutants.
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Deficiency in initiation factors of protein synthesis induced by phage T7 in E. coli F(+) strains.噬菌体T7在大肠杆菌F(+)菌株中诱导的蛋白质合成起始因子缺乏。
FEBS Lett. 1972 Oct 15;27(1):1-4. doi: 10.1016/0014-5793(72)80394-6.
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In vitro synthesis of bacteriophage lysozyme.噬菌体溶菌酶的体外合成
Nature. 1967 Aug 5;215(5101):588-91. doi: 10.1038/215588a0.
7
T7 translational control mechanisms and their inhibiton by F factors.T7 翻译控制机制及其受 F 因子的抑制作用。
Nat New Biol. 1971 May 12;231(19):37-41. doi: 10.1038/newbio231037a0.
8
Synthesis in vitro of type 5 adenovirus capsid proteins.5型腺病毒衣壳蛋白的体外合成
J Virol. 1972 Jun;9(6):973-80. doi: 10.1128/JVI.9.6.973-980.1972.
9
Phage T7 lysozyme mRNA transcription and translation in vivo and in vitro.噬菌体T7溶菌酶mRNA在体内和体外的转录与翻译。
Biochem Biophys Res Commun. 1971 Oct 15;45(2):315-20. doi: 10.1016/0006-291x(71)90820-5.
10
Comparisons of F factors and R factors: existence of independent regulation groups in F factors.F 因子与 R 因子的比较:F 因子中独立调控基团的存在
J Bacteriol. 1970 Jul;103(1):81-8. doi: 10.1128/jb.103.1.81-88.1970.

在感染了含有F'(PIF+)附加体的细胞中存在非翻译T7晚期mRNA的证据。

Evidence for the presence of nontranslated T7 late mRNA in infected F'(PIF+) episome-containing cells.

作者信息

Blumberg D D, Malamy M H

出版信息

J Virol. 1974 Feb;13(2):378-85. doi: 10.1128/JVI.13.2.378-385.1974.

DOI:10.1128/JVI.13.2.378-385.1974
PMID:4589854
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC355307/
Abstract

The inability of T7 to develop in cells of Escherichia coli containing F(+) or substituted F' episomes is a result of the failure to synthesize late proteins; no in vivo translation of mRNA species synthesized by the T7 RNA polymerase occurs. Further experiments have been performed to measure the amount of late mRNA in T7-infected F'(PIF(+)) cells. (We have designated the property of phage inhibition of F factors as PIF; the wild-type episome is therefore F'[PIF(+)].) T7 late proteins were synthesized in vitro by using a system programed with RNA extracted from T7-infected F(-) and F'(PIF(+)) cells. The T7 lysozyme, product of gene 3.5, and the gene 10 head protein were assayed. The following results were obtained: (i) mRNA capable of supporting in vitro synthesis of lysozyme and the gene 10 head protein is present in T7-infected F'(PIF(+)) cells; (ii) lysozyme mRNA extracted from T7-infected F'(PIF(+)) cells is present at 70 to 75% of the level found in T7-infected F(-) cells; (iii) gene 10 mRNA is present at 35 to 78% of the level found in T7-infected F(-) cells. No in vivo synthesis of either lysozyme or gene 10 protein can be detected in T7-infected F'(PIF(+)) cells although normal synthesis of these proteins occurs in F(-) cells. These findings confirm that the block in T7 development in F'(PIF(+)) cells results from the failure to translate late classes of T7 RNA.

摘要

T7无法在含有F(+)或取代型F'附加体的大肠杆菌细胞中生长,这是由于无法合成晚期蛋白质所致;T7 RNA聚合酶合成的mRNA种类在体内无法进行翻译。已开展进一步实验来测定T7感染的F'(PIF(+))细胞中晚期mRNA的量。(我们将噬菌体对F因子的抑制特性命名为PIF;因此野生型附加体为F'[PIF(+)]。)通过使用由从T7感染的F(-)和F'(PIF(+))细胞中提取的RNA编程的系统,在体外合成了T7晚期蛋白质。对基因3.5的产物T7溶菌酶和基因10头部蛋白进行了测定。得到以下结果:(i)能够支持溶菌酶和基因10头部蛋白体外合成的mRNA存在于T7感染的F'(PIF(+))细胞中;(ii)从T7感染的F'(PIF(+))细胞中提取的溶菌酶mRNA的含量为T7感染的F(-)细胞中所发现水平的70%至75%;(iii)基因10 mRNA的含量为T7感染的F(-)细胞中所发现水平的35%至78%。在T7感染的F'(PIF(+))细胞中无法检测到溶菌酶或基因10蛋白的体内合成,尽管这些蛋白在F(-)细胞中能正常合成。这些发现证实,F'(PIF(+))细胞中T7生长的阻滞是由于未能翻译T7 RNA的晚期种类所致。