Unusually long-lived pause required for regulation of a Rho-dependent transcription terminator

Up to half of all transcription termination events in bacteria rely on the RNA-dependent helicase Rho. However, the nucleic acid sequences that promote Rho-dependent termination remain poorly characterized. Defining the molecular determinants that confer Rho-dependent termination is especially impor...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 111; no. 19; pp. E1999 - E2007
Main Authors Hollands, Kerry, Sevostiyanova, Anastasia, Groisman, Eduardo A.
Format Journal Article
LanguageEnglish
Published United States National Academy of Sciences 13.05.2014
National Acad Sciences
SeriesPNAS Plus
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Summary:Up to half of all transcription termination events in bacteria rely on the RNA-dependent helicase Rho. However, the nucleic acid sequences that promote Rho-dependent termination remain poorly characterized. Defining the molecular determinants that confer Rho-dependent termination is especially important for understanding how such terminators can be regulated in response to specific signals. Here, we identify an extraordinarily long-lived pause at the site where Rho terminates transcription in the 5′-leader region of the Mg ²⁺ transporter gene mgtA in Salmonella enterica . We dissect the sequence elements required for prolonged pausing in the mgtA leader and establish that the remarkable longevity of this pause is required for a riboswitch to stimulate Rho-dependent termination in the mgtA leader region in response to Mg ²⁺ availability. Unlike Rho-dependent terminators described previously, where termination occurs at multiple pause sites, there is a single site of transcription termination directed by Rho in the mgtA leader. Our data suggest that Rho-dependent termination events that are subject to regulation may require elements distinct from those operating at constitutive Rho-dependent terminators.
Bibliography:http://dx.doi.org/10.1073/pnas.1319193111
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Author contributions: K.H. and E.A.G. designed research; K.H. and A.S. performed research; K.H., A.S., and E.A.G. analyzed data; and K.H. and E.A.G. wrote the paper.
1Present address: DuPont Central Research and Development, Experimental Station, Wilmington, DE 19803.
Edited by Jeffrey W. Roberts, Cornell University, Ithaca, NY, and approved April 2, 2014 (received for review October 10, 2013)
ISSN:0027-8424
1091-6490
1091-6490
DOI:10.1073/pnas.1319193111