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A non-canonical promoter element drives spurious transcription of horizontally acquired bacterial genes

Emily A. Warman, Shivani Singh, Alicia G. Gubieda, David C. Grainger

2020Nucleic Acids Research35 citationsDOIOpen Access PDF

Abstract

RNA polymerases initiate transcription at DNA sequences called promoters. In bacteria, the best conserved promoter feature is the AT-rich -10 element; a sequence essential for DNA unwinding. Further elements, and gene regulatory proteins, are needed to recruit RNA polymerase to the -10 sequence. Hence, -10 elements cannot function in isolation. Many horizontally acquired genes also have a high AT-content. Consequently, sequences that resemble the -10 element occur frequently. As a result, foreign genes are predisposed to spurious transcription. However, it is not clear how RNA polymerase initially recognizes such sequences. Here, we identify a non-canonical promoter element that plays a key role. The sequence, itself a short AT-tract, resides 5 base pairs upstream of otherwise cryptic -10 elements. The AT-tract alters DNA conformation and enhances contacts between the DNA backbone and RNA polymerase.

Topics & Concepts

BiologyTranscription (linguistics)RNA polymeraseGeneticsBase pairPromoterGeneRNA polymerase IIPolymeraseResponse elementRNAGene expressionLinguisticsPhilosophyBacterial Genetics and BiotechnologyRNA and protein synthesis mechanismsGenomics and Phylogenetic Studies
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