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Series GSE48221 Query DataSets for GSE48221
Status Public on Jun 24, 2013
Title A small RNA activates CFA synthase by a reprogrammable mechanism of mRNA stabilization
Organism Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344
Experiment type Expression profiling by array
Summary Small RNAs use a diversity of well-characterized mechanisms to repress mRNAs, but how they activate gene expression at the mRNA level remains not well understood. The predominant activation mechanism of Hfq-associated small RNAs has been translational control whereby base-pairing with the target prevents the formation of an intrinsic inhibitory structure in the mRNA and promotes translation initiation. Here, we report a translation-independent mechanism whereby the small RNA RydC selectively activates the longer of two isoforms of cfa mRNA (encoding cyclopropane fatty acid synthase) in Salmonella enterica. Target activation is achieved through seed pairing of the pseudoknot-exposed, conserved 5' end of RydC to an upstream region of the cfa mRNA. The seed pairing stabilizes the messenger, likely by interfering directly with RNase E-mediated decay in the 5' untranslated region. Intriguingly, this activation mechanism is fully generic in that it can be reprogrammed to other seed pairing small RNAs, suggesting this mechanism may be utilised in the design of RNA-controlled synthetic circuits. Physiologically, RydC is the first small RNA known to regulate membrane stability.
 
Overall design To determine the targets of the small regulatory RNA RydC in S. Typhimurium, we looked at the effect of a short pulse of RydC over-expression on the Salmonella transcriptome. To achieve over-expression, the rydC gene was cloned in the pBAD plasmid and induced with 0.2% L-arabinose for 10 min. We then extracted the total RNA for transcriptional profiling. A strain carrying the pBAD plasmid w/o insert was used as negative control (also induced by L-arabinose). 2 biological replicates were performed. This sRNA target identification strategy has been described in Papenfort et al; Molecular Microbiology (2006) 62(6), 1674–1688.
 
Contributor(s) Fröhlich KS, Papenfort K, Fekete A, Vogel J
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Submission date Jun 24, 2013
Last update date Jun 24, 2013
Contact name Kai Papenfort
Organization name IMIB Würzburg
Department RNA Biology
Street address Josef-Schneider Str.2/BAU D15
City Würzburg
State/province Würzburg
ZIP/Postal code 97080
Country Germany
 
Platforms (1)
GPL11416 SALSIFY, Agilent-026881 S. Typhimurim
Samples (4)
GSM1173066 pBAD-ctr 1
GSM1173067 pBAD-ctr 2
GSM1173068 pBAD-RydC 1
Relations
BioProject PRJNA209314

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE48221_RAW.tar 19.4 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table
Processed data provided as supplementary file

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