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大肠杆菌启动子。I. 与间隔类别、特异性、重复子结构和三维组织相关的共有序列

Escherichia coli promoters. I. Consensus as it relates to spacing class, specificity, repeat substructure, and three-dimensional organization.

作者信息

O'Neill M C

机构信息

Department of Biological Sciences, University of Maryland, Baltimore County 21228.

出版信息

J Biol Chem. 1989 Apr 5;264(10):5522-30.

PMID:2647720
Abstract

Fifty-two of the best characterized Escherichia coli promoters in the Hawley and McClure [1983) Nucleic Acids Res. 8, 2237-2255) listing were used to determine the distribution of information content in promoters and to describe the basic features underlying the existence of several different promoter spacing classes, which are defined by the number of bases separating the -35 and -10 regions. The contact regions at -35 and -10 do not, on the average, contain sufficient information to specify a promoter. The search for additional specifying bases led to two conclusions: 1) the consensus nucleotide sequence in the noncontact regions of a promoter appears to be distinct for each of the major promoter spacing classes; 2) promoters appear to contain a 15-20 base subset of the 40-50 additional optimal noncontact bases. This improved view of the extended consensus sequence allows the detection of a 10-base degenerate palindrome which may be the basic unit of promoter structure. Contiguous direct repeats of this sequence produce a sequence closely related to the consensus for the 18-base pair spacing class. This underlying structure is also evidenced in the 17- and 16-base pair spacing classes; however, the start points of the fourth and subsequent repetitions of the sequence element are moved one and two bases upstream, respectively, relative to their location in the 18-base pair spacing class. These consensus sequences, when viewed in a helical format, all present the opportunity for two alternative sets of a dyad repeat. The -35 region is common to both sets and is paired with an extended -10 region in one set and with a pseudo-10 region in the other. Possible implications of these arrangements are discussed.

摘要

霍利和麦克卢尔[1983年,《核酸研究》8卷,2237 - 2255页]列出的52个特征最为明确的大肠杆菌启动子,被用于确定启动子中信息含量的分布,并描述几种不同启动子间隔类存在的基本特征,这些间隔类是由-35区和-10区之间的碱基数量定义的。-35区和-10区的接触区域平均而言并不包含足以确定一个启动子的信息。对额外确定碱基的搜索得出了两个结论:1)启动子非接触区域的共有核苷酸序列对于每个主要的启动子间隔类似乎都是不同的;2)启动子似乎包含40 - 50个额外的最佳非接触碱基中的一个15 - 20个碱基的子集。对扩展共有序列的这种改进看法使得能够检测到一个10碱基的简并回文序列,它可能是启动子结构的基本单元。该序列的连续直接重复产生一个与18碱基对间隔类的共有序列密切相关的序列。这种潜在结构在17和16碱基对间隔类中也有体现;然而,该序列元件第四次及后续重复的起始点相对于它们在18碱基对间隔类中的位置分别向上游移动了1个和2个碱基。当以螺旋形式查看这些共有序列时,它们都提供了形成两组二元重复的机会。-35区在两组中是共同的,并且在一组中与一个扩展的-10区配对,在另一组中与一个假-10区配对。讨论了这些排列可能的影响。

相似文献

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Escherichia coli promoters. I. Consensus as it relates to spacing class, specificity, repeat substructure, and three-dimensional organization.大肠杆菌启动子。I. 与间隔类别、特异性、重复子结构和三维组织相关的共有序列
J Biol Chem. 1989 Apr 5;264(10):5522-30.
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Escherichia coli promoters. II. A spacing class-dependent promoter search protocol.大肠杆菌启动子。II. 一种依赖间隔类别的启动子搜索方案。
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Analysis of E. coli promoter sequences.大肠杆菌启动子序列分析。
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The organization of open complexes between Escherichia coli RNA polymerase and DNA fragments carrying promoters either with or without consensus -35 region sequences.大肠杆菌RNA聚合酶与携带具有或不具有一致-35区域序列的启动子的DNA片段之间开放复合物的组织。
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Specific contacts between the bacteriophage T3, T7, and SP6 RNA polymerases and their promoters.噬菌体T3、T7和SP6 RNA聚合酶与其启动子之间的特异性相互作用。
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Investigations of Escherichia coli promoter sequences with artificial neural networks: new signals discovered upstream of the transcriptional startpoint.利用人工神经网络对大肠杆菌启动子序列进行的研究:在转录起始点上游发现新信号。
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DNA sequence elements located immediately upstream of the -10 hexamer in Escherichia coli promoters: a systematic study.大肠杆菌启动子中位于 -10 六聚体紧邻上游的 DNA 序列元件:一项系统性研究。
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Promoter recognition by Escherichia coli RNA polymerase. Effects of single base pair deletions and insertions in the spacer DNA separating the -10 and -35 regions are dependent on spacer DNA sequence.大肠杆菌RNA聚合酶对启动子的识别。在分隔-10区和-35区的间隔DNA中单个碱基对缺失和插入的影响取决于间隔DNA序列。
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DNA sequences of random origin as probes of Escherichia coli promoter architecture.随机来源的DNA序列作为大肠杆菌启动子结构的探针。
J Biol Chem. 1988 Oct 15;263(29):14724-31.

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