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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.

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/2d05/208440/21bd388e3134/jbacter01043-0386-a.jpg

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