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噬菌体Mu的Mor蛋白需要σ70来激活Mu中间启动子。

Bacteriophage Mu Mor protein requires sigma 70 to activate the Mu middle promoter.

作者信息

Mathee K, Howe M M

机构信息

Department of Microbiology and Immunology, University of Tennessee-Memphis 38163.

出版信息

J Bacteriol. 1993 Sep;175(17):5314-23. doi: 10.1128/jb.175.17.5314-5323.1993.

DOI:10.1128/jb.175.17.5314-5323.1993
PMID:8366019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC206584/
Abstract

Transcription during the bacteriophage Mu lytic cycle occurs in three phases: early, middle, and late. Middle transcription requires the early gene product Mor for its activation. Mor protein overproduction was accomplished by fusing the mor gene to an efficient phage T7 promoter and translation initiation region. A protein fraction highly enriched for Escherichia coli RNA polymerase (E sigma 70) from the Mor-overproducing strain was able to activate transcription from both the tac promoter (Ptac) and the Mu middle promoter (Pm) in vitro. Transcription initiation from Pm was Mor dependent, and the RNA 5' end was identical to that of in vivo RNA. Addition of anti-sigma 70 antibody to transcription reactions containing Ptac and Pm resulted in inhibition of transcription from both promoters; addition of purified sigma 70 restored transcription. These results indicate that Mor-dependent activation requires sigma 70 and therefore imply that Mor is not an alternate sigma factor. This conclusion was further substantiated by a reconstitution experiment with purified proteins in which all three components, Mor, sigma 70, and core RNA polymerase, were required for Pm-dependent transcription in vitro. The sigma 70 dependence of Mor-specific transcription and the amino acid sequence similarity between Mor and C (an activator for Mu late transcription) both support the hypothesis that Mor functions mechanistically as an activator protein.

摘要

噬菌体Mu裂解周期中的转录分为三个阶段:早期、中期和晚期。中期转录需要早期基因产物Mor来激活。通过将mor基因与高效噬菌体T7启动子和翻译起始区域融合,实现了Mor蛋白的过量表达。从Mor过量表达菌株中高度富集大肠杆菌RNA聚合酶(E sigma 70)的蛋白质组分能够在体外激活来自tac启动子(Ptac)和Mu中期启动子(Pm)的转录。从Pm起始的转录依赖于Mor,且RNA 5'末端与体内RNA相同。向含有Ptac和Pm的转录反应中添加抗sigma 70抗体导致两个启动子的转录均受到抑制;添加纯化的sigma 70可恢复转录。这些结果表明,Mor依赖的激活需要sigma 70,因此意味着Mor不是一个替代的sigma因子。用纯化蛋白进行的重组实验进一步证实了这一结论,在该实验中,体外依赖Pm的转录需要Mor、sigma 70和核心RNA聚合酶这三个组分。Mor特异性转录对sigma 70的依赖性以及Mor与C(Mu晚期转录的激活剂)之间的氨基酸序列相似性均支持Mor作为激活蛋白发挥作用的假说。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60bd/206584/24adc19b7369/jbacter00059-0035-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60bd/206584/4cfe1f44f03e/jbacter00059-0032-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60bd/206584/36a05c36aa68/jbacter00059-0033-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60bd/206584/d1dd8769d4bc/jbacter00059-0033-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60bd/206584/4fe6126f0ef5/jbacter00059-0034-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60bd/206584/cebc363aa147/jbacter00059-0034-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60bd/206584/24adc19b7369/jbacter00059-0035-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60bd/206584/4cfe1f44f03e/jbacter00059-0032-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60bd/206584/36a05c36aa68/jbacter00059-0033-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60bd/206584/d1dd8769d4bc/jbacter00059-0033-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60bd/206584/4fe6126f0ef5/jbacter00059-0034-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60bd/206584/cebc363aa147/jbacter00059-0034-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60bd/206584/24adc19b7369/jbacter00059-0035-a.jpg

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引用本文的文献

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Microbiologyopen. 2014 Aug;3(4):470-83. doi: 10.1002/mbo3.181. Epub 2014 Jun 10.
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Binding of the C-terminal domain of the alpha subunit of RNA polymerase to the phage mu middle promoter.

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Transcription activation by the bacteriophage Mu Mor protein: analysis of promoter mutations in Pm identifies a new region required for promoter function.噬菌体Mu Mor蛋白介导的转录激活:Pm中启动子突变分析确定了启动子功能所需的一个新区域。
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