@article {Gordon2015-tp,
	title = {A search for ribonucleic antiterminator sites in bacterial genomes: Not only antitermination?},
	journal = {J. Mol. Microbiol. Biotechnol.},
	volume = {25},
	number = {2-3},
	year = {2015},
	pages = {143{\textendash}153},
	publisher = {S. Karger AG},
	abstract = {BglG/LicT-like proteins are transcriptional antiterminators that prevent termination of transcription at intrinsic terminators by binding to ribonucleic antiterminator (RAT) sites and stabilizing an RNA conformation which is mutually exclusive with the terminator structure. The known RAT sites, which are located in intergenic regions of sugar utilization operons, show low sequence conservation but significant structural analogy. To assess the prevalence of RATs in bacterial genomes, we employed bioinformatic tools that describe RNA motifs based on both sequence and structural constraints. Using descriptors with different stringency, we searched the genomes of Escherichiacoli K12, uropathogenic E. coli and Bacillus subtilis for putative RATs. Our search identified all known RATs and additional putative RAT elements. Surprisingly, most putative RATs do not overlap an intrinsic terminator and many reside within open reading frames (ORFs). The ability of one of the putative RATs, which is located within an antiterminator-encoding ORF and does not overlap a terminator, to bind to its cognate antiterminator protein in vitro and in vivo was confirmed experimentally. Our results suggest that the capacity of RAT elements has been exploited during evolution to mediate activities other than antitermination, for example control of transcription elongation or of RNA stability.},
	author = {Gordon, Noa and Rosenblum, Ronen and Nussbaum-Shochat, Anat and Eliahoo, Elad and Amster-Choder, Orna}
}
