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噬菌体Mu中间启动子Pm含有一个部分上游元件(UP元件)。

The phage Mu middle promoter Pm contains a partial UP element.

作者信息

Ma Ji, Howe Martha M

机构信息

Department of Microbiology, Immunology & Biochemistry, University of Tennessee Health Science Center, Memphis, Tennessee 38163.

Department of Microbiology, Immunology & Biochemistry, University of Tennessee Health Science Center, Memphis, Tennessee 38163

出版信息

G3 (Bethesda). 2015 Feb 2;5(4):507-16. doi: 10.1534/g3.114.013607.

Abstract

There are three phases of transcription during lytic development of bacteriophage Mu: early, middle, and late. Transcription from the middle phase promoter Pm requires the activator protein Mor. In the presence of Mor, transcription from Pm is carried out by the Escherichia coli RNA polymerase holoenzyme containing σ(70). A Mor dimer binds to two 5-bp inverted repeats within a 16-bp element centered at -43.5 in Pm, replacing the normal -35 element contacted by RNA polymerase (RNAP). In this study random and targeted mutagenesis of the sequence upstream (-88 to -52) of the Mor binding site was performed to determine whether Pm also contains an UP element for binding of the RNAP α subunit, thereby stimulating transcription. The results demonstrated that mutations upstream of -57 had no effect on Pm activity in vivo, assayed by expression of lacZ fused downstream of a wild-type or mutant Pm. Mutations at positions -57 through -52 led to decreased transcription from Pm, consistent with the presence of an UP element. In DNase I footprinting and gel mobility shift assays, paired mutations at positions -55 and -54 did not affect Mor binding but decreased the synergistic binding of Mor with histidine tagged α (His-α), indicating that His-α binds to Pm in a sequence- and/or structure-specific manner. Taken together, these results demonstrate that Pm has a strong proximal UP element subsite, but lacks a distal subsite.

摘要

在噬菌体Mu的裂解发育过程中有三个转录阶段:早期、中期和晚期。从中期启动子Pm进行转录需要激活蛋白Mor。在Mor存在的情况下,Pm的转录由含有σ(70)的大肠杆菌RNA聚合酶全酶进行。一个Mor二聚体与Pm中位于-43.5中心的一个16 bp元件内的两个5 bp反向重复序列结合,取代了RNA聚合酶(RNAP)接触的正常-35元件。在本研究中,对Mor结合位点上游(-88至-52)的序列进行了随机和定向诱变,以确定Pm是否也含有用于RNAP α亚基结合的上游元件(UP元件),从而刺激转录。结果表明,在野生型或突变型Pm下游融合lacZ的表达所测定的体内,-57上游的突变对Pm活性没有影响。-57至-52位的突变导致Pm转录减少,这与存在UP元件一致。在DNase I足迹实验和凝胶迁移率变动分析中,-55和-54位的配对突变不影响Mor结合,但降低了Mor与组氨酸标记的α(His-α)的协同结合,表明His-α以序列和/或结构特异性方式与Pm结合。综上所述,这些结果表明Pm有一个强的近端UP元件亚位点,但缺乏远端亚位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c28f/4390567/a360b2d5526b/507f1.jpg

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