Abstract
Predicting the location and strength of promoters from genomic sequence requires accurate sequenced-based promoter models. We present the first model of a full-length bacterial promoter, encompassing both upstream sequences (UP-elements) and core promoter modules, based on a set of 60 promoters dependent on σ E, an alternative ECF-type σ factor. UP-element contribution, best described by the length and frequency of A-and T-tracts, in combination with a PWM-based core promoter model, accurately predicted promoter strength both in vivo and in vitro. This model also distinguished active from weak/inactive promoters. Systematic examination of promoter strength as a function of RNA polymerase (RNAP) concentration revealed that UP-element contribution varied with RNAP availability and that the σ E regulon is comprised of two promoter types, one of which is active only at high concentrations of RNAP. Distinct promoter types may be a general mechanism for increasing the regulatory capacity of the ECF group of alternative σ's. Our findings provide important insights into the sequence requirements for the strength and function of full-length promoters and establish guidelines for promoter prediction and for forward engineering promoters of specific strengths. © 2011 The Author(s).
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CITATION STYLE
Rhodius, V. A., Mutalik, V. K., & Gross, C. A. (2012). Predicting the strength of UP-elements and full-length E. coli σ e promoters. Nucleic Acids Research, 40(7), 2907–2924. https://doi.org/10.1093/nar/gkr1190
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