Literature DB >> 2647720

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

M C O'Neill1.   

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.

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Year:  1989        PMID: 2647720

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  41 in total

1.  Role and mechanism of action of C. PvuII, a regulatory protein conserved among restriction-modification systems.

Authors:  R M Vijesurier; L Carlock; R M Blumenthal; J C Dunbar
Journal:  J Bacteriol       Date:  2000-01       Impact factor: 3.490

2.  Identification and analysis of 'extended -10' promoters in Escherichia coli.

Authors:  Jennie E Mitchell; Dongling Zheng; Stephen J W Busby; Stephen D Minchin
Journal:  Nucleic Acids Res       Date:  2003-08-15       Impact factor: 16.971

3.  The D-galactose dehydrogenase gene from Pseudomonas fluorescens: characterization of mutations leading to increased expression in Escherichia coli.

Authors:  S Fiedler; P Buckel
Journal:  Appl Microbiol Biotechnol       Date:  1990-07       Impact factor: 4.813

4.  An assessment of neural network and statistical approaches for prediction of E. coli promoter sites.

Authors:  P B Horton; M Kanehisa
Journal:  Nucleic Acids Res       Date:  1992-08-25       Impact factor: 16.971

5.  Training back-propagation neural networks to define and detect DNA-binding sites.

Authors:  M C O'Neill
Journal:  Nucleic Acids Res       Date:  1991-01-25       Impact factor: 16.971

6.  Regulation of excision genes of the Bacteroides conjugative transposon CTnDOT.

Authors:  Kyung Moon; Nadja B Shoemaker; Jeffrey F Gardner; Abigail A Salyers
Journal:  J Bacteriol       Date:  2005-08       Impact factor: 3.490

7.  Dual transcriptional initiation sites from the pyrC promoter control expression of the gene in Salmonella typhimurium.

Authors:  K I Sørensen; J Neuhard
Journal:  Mol Gen Genet       Date:  1991-02

8.  Isolation of DNA damage-inducible promoters in Escherichia coli: regulation of polB (dinA), dinG, and dinH by LexA repressor.

Authors:  L K Lewis; M E Jenkins; D W Mount
Journal:  J Bacteriol       Date:  1992-05       Impact factor: 3.490

9.  Application of a new method of pattern recognition in DNA sequence analysis: a study of E. coli promoters.

Authors:  N N Alexandrov; A A Mironov
Journal:  Nucleic Acids Res       Date:  1990-04-11       Impact factor: 16.971

10.  Purines are required at the 5' ends of newly initiated RNAs for optimal RNA polymerase III gene expression.

Authors:  G N Zecherle; S Whelen; B D Hall
Journal:  Mol Cell Biol       Date:  1996-10       Impact factor: 4.272

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