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噬菌体Mu C操纵子转录本的表征

Characterization of the C operon transcript of bacteriophage Mu.

作者信息

Stoddard S F, Howe M M

机构信息

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

出版信息

J Bacteriol. 1990 Jan;172(1):361-71. doi: 10.1128/jb.172.1.361-371.1990.

DOI:10.1128/jb.172.1.361-371.1990
PMID:2136735
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC208440/
Abstract

Mu transcription occurs in three phases: early, middle, and late. Middle transcription occurs in the region of the C gene, which encodes the transactivator for late transcription. A middle promoter, Pm, was previously localized between 0.28 and 1.2 kilobase pairs upstream of C. We used S1 nuclease mapping with both unlabeled and radiolabeled capped RNAs from induced lysogens to characterize C transcription and identify its promoter. The C transcription initiation site was localized to a 4-base-pair region, approximately 740 base pairs upstream of C within the region containing Pm. Transcription of C was activated between 4 and 8 min after induction of cts and Cam lysogens and increased throughout the lytic cycle. Significant C transcription did not occur in replication-defective Aam lysogens. These kinetic and regulatory characteristics identify the C transcript as a middle RNA species and demonstrate that Pm is the C promoter. DNA sequence analysis of the Pm region showed a good -10, but poor -35, site homology to the Escherichia coli RNA polymerase consensus sequence. In addition, the sequence demonstrated that C is the distal gene in a middle operon containing several open reading frames. S1 mapping also showed an upstream transcript with a 3' end in the Pm region at a sequence strongly resembling a Rho-independent terminator. The regulatory characteristics of this RNA are consistent with this terminator, t9.2, being the early operon terminator.

摘要

Mu转录分为三个阶段:早期、中期和晚期。中期转录发生在C基因区域,该基因编码晚期转录的反式激活因子。一个中期启动子Pm先前定位于C基因上游0.28至1.2千碱基对之间。我们使用S1核酸酶图谱技术,结合来自诱导溶原菌的未标记和放射性标记的加帽RNA,来表征C转录并鉴定其启动子。C转录起始位点定位于一个4碱基对区域,该区域位于包含Pm的区域内,C基因上游约740碱基对处。cts和Cam溶原菌诱导后4至8分钟,C转录被激活,并在整个裂解周期中增加。在复制缺陷的Aam溶原菌中未发生显著的C转录。这些动力学和调控特征将C转录本鉴定为中期RNA种类,并证明Pm是C启动子。对Pm区域的DNA序列分析显示,与大肠杆菌RNA聚合酶共有序列的-10位点同源性良好,但-35位点同源性较差。此外,该序列表明C是一个包含几个开放阅读框的中期操纵子中的远端基因。S1图谱还显示在Pm区域有一个上游转录本,其3'端位于一个与不依赖Rho的终止子非常相似的序列处。该RNA的调控特征与这个终止子t9.2作为早期操纵子终止子一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d05/208440/e3c131770fc5/jbacter01043-0390-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d05/208440/21bd388e3134/jbacter01043-0386-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d05/208440/7bc60bf3d6c6/jbacter01043-0387-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d05/208440/d24397441369/jbacter01043-0388-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d05/208440/23df8d0296cc/jbacter01043-0389-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d05/208440/e3c131770fc5/jbacter01043-0390-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d05/208440/21bd388e3134/jbacter01043-0386-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d05/208440/7bc60bf3d6c6/jbacter01043-0387-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d05/208440/d24397441369/jbacter01043-0388-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d05/208440/23df8d0296cc/jbacter01043-0389-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d05/208440/e3c131770fc5/jbacter01043-0390-a.jpg

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引用本文的文献

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Binding of the C-terminal domain of the alpha subunit of RNA polymerase to the phage mu middle promoter.RNA聚合酶α亚基的C末端结构域与噬菌体μ中间启动子的结合。
J Bacteriol. 2004 Dec;186(23):7858-64. doi: 10.1128/JB.186.23.7858-7864.2004.
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Distortion in the spacer region of Pm during activation of middle transcription of phage Mu.

本文引用的文献

1
Bacteriophage Mu DNA replication is stimulated by non-essential early functions.噬菌体Mu DNA复制受非必需早期功能的刺激。
Mol Gen Genet. 1982;186(1):135-9. doi: 10.1007/BF00422925.
2
Resolution of a hybrid cointegrate between transposons Tn501 and Tn1721 defines the recombination site.转座子Tn501和Tn1721之间杂种共整合体的解离确定了重组位点。
Mol Gen Genet. 1984;193(1):162-6. doi: 10.1007/BF00327431.
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Sequence of the site-specific recombinase gene cin and of its substrates serving in the inversion of the C segment of bacteriophage P1.
噬菌体Mu中间转录激活过程中Pm间隔区的畸变。
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Regulatory factors acting at the bacteriophage Mu middle promoter.作用于噬菌体Mu中间启动子的调控因子。
J Bacteriol. 1996 Mar;178(6):1585-92. doi: 10.1128/jb.178.6.1585-1592.1996.
5
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。
Nucleic Acids Res. 1996 Feb 1;24(3):450-7. doi: 10.1093/nar/24.3.450.
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Bacteriophage Mu Mor protein requires sigma 70 to activate the Mu middle promoter.噬菌体Mu的Mor蛋白需要σ70来激活Mu中间启动子。
J Bacteriol. 1993 Sep;175(17):5314-23. doi: 10.1128/jb.175.17.5314-5323.1993.
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Identification and characterization of the terminators of the lys and P transcripts of bacteriophage Mu.噬菌体Mu的lys和P转录本终止子的鉴定与表征
J Bacteriol. 1994 Feb;176(4):1111-20. doi: 10.1128/jb.176.4.1111-1120.1994.
8
Identification of a positive regulator of the Mu middle operon.鉴定Mu中间操纵子的一个正调控因子。
J Bacteriol. 1990 Dec;172(12):6641-50. doi: 10.1128/jb.172.12.6641-6650.1990.
噬菌体P1的C片段倒置中起作用的位点特异性重组酶基因cin及其底物的序列。
EMBO J. 1983;2(10):1733-40. doi: 10.1002/j.1460-2075.1983.tb01650.x.
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DNA inversions in the chromosome of Escherichia coli and in bacteriophage Mu: relationship to other site-specific recombination systems.大肠杆菌染色体及噬菌体Mu中的DNA倒位:与其他位点特异性重组系统的关系
Proc Natl Acad Sci U S A. 1983 Sep;80(17):5355-8. doi: 10.1073/pnas.80.17.5355.
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The early promoter of bacteriophage Mu: definition of the site of transcript initiation.噬菌体Mu的早期启动子:转录起始位点的定义
Nucleic Acids Res. 1983 Aug 25;11(16):5483-95. doi: 10.1093/nar/11.16.5483.
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Ner, a cro-like function of bacteriophage Mu.Ner,噬菌体Mu的一种cro样功能。
Virology. 1982 Nov;123(1):19-28. doi: 10.1016/0042-6822(82)90291-4.
7
Transposon-mediated site-specific recombination: identification of three binding sites for resolvase at the res sites of gamma delta and Tn3.转座子介导的位点特异性重组:在γδ和Tn3的res位点鉴定出解离酶的三个结合位点。
Cell. 1982 Aug;30(1):19-27. doi: 10.1016/0092-8674(82)90007-1.
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Instability of transposase activity: evidence from bacteriophage mu DNA replication.转座酶活性的不稳定性:来自噬菌体μ DNA复制的证据。
Cell. 1982 May;29(1):219-25. doi: 10.1016/0092-8674(82)90106-4.
9
Correlation of the genetic and physical maps in the central region of the bacteriophage Mu genome.噬菌体Mu基因组中心区域遗传图谱与物理图谱的相关性
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Involvement of the invertible G segment in bacteriophage mu tail fiber biosynthesis.可逆G片段参与噬菌体μ尾丝生物合成。
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