Suppr超能文献

噬菌体T3和T7的DNA包装对转录的依赖性

Transcription dependence of DNA packaging of bacteriophages T3 and T7.

作者信息

Hashimoto C, Fujisawa H

机构信息

Department of Botany, Faculty of Science, Kyoto University, Japan.

出版信息

Virology. 1992 Nov;191(1):246-50. doi: 10.1016/0042-6822(92)90186-s.

Abstract

T3 and T7 phages package homologous DNA more efficiently than heterologous DNA and recombinant plasmids carrying DNA sequences necessary for DNA packaging (pac sequence). The pac sequence contains a promoter for phage RNA polymerase and transcription from the promoter is necessary for DNA packaging. T3 and T7 RNA polymerases are stringently specific for their own promoters. To examine the relationship between DNA packaging and transcription, we constructed a cleared in vitro system for packaging T3 or T7 DNA containing an ammonium sulfate fractionate of a high-speed supernatant of phage-infected cells. In the system, DNA packaging required GTP and was inhibited by the 3'-deoxy analog of GTP, ATP, or CTP. The DNA packaging activity paralleled the transcriptional activity, assayed by incorporation of [32P]UTP into acid-insoluble material. In the system, homologous DNA was packaged more efficiently than heterologous DNA, but heterologous DNA was packaged as efficiently as homologous DNA by the addition of heterologous phage RNA polymerase, demonstrating that the transcriptional specificity determines the DNA packaging specificity of T3 and T7.

摘要

T3和T7噬菌体包装同源DNA的效率高于异源DNA以及携带DNA包装所需DNA序列(pac序列)的重组质粒。pac序列包含噬菌体RNA聚合酶的启动子,从该启动子进行转录是DNA包装所必需的。T3和T7 RNA聚合酶对其自身的启动子具有严格的特异性。为了研究DNA包装与转录之间的关系,我们构建了一个经过澄清的体外系统,用于包装含有噬菌体感染细胞高速上清液硫酸铵分级分离物的T3或T7 DNA。在该系统中,DNA包装需要GTP,并受到GTP、ATP或CTP的3'-脱氧类似物的抑制。通过将[32P]UTP掺入酸不溶性物质来测定DNA包装活性与转录活性平行。在该系统中,同源DNA的包装效率高于异源DNA,但通过添加异源噬菌体RNA聚合酶,异源DNA的包装效率与同源DNA一样高,这表明转录特异性决定了T3和T7的DNA包装特异性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验