共 51 条
Multiple factors dictate target selection by Hfq-binding small RNAs
被引:95
作者:
Beisel, Chase L.
[1
]
Updegrove, Taylor B.
[1
]
Janson, Ben J.
[1
]
Storz, Gisela
[1
]
机构:
[1] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Cell Biol & Metab Program, Bethesda, MD 20892 USA
关键词:
base-pairing;
Escherichia coli;
Spot;
42;
target prediction;
ESCHERICHIA-COLI;
SOLUBLE-RNA;
POSTTRANSCRIPTIONAL CONTROL;
TRANSLATIONAL INITIATION;
CATABOLITE REPRESSION;
REGULATORY RNAS;
GENE-EXPRESSION;
SPOT;
42;
PREDICTION;
GCVB;
D O I:
10.1038/emboj.2012.52
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Hfq-binding small RNAs (sRNAs) in bacteria modulate the stability and translational efficiency of target mRNAs through limited base-pairing interactions. While these sRNAs are known to regulate numerous mRNAs as part of stress responses, what distinguishes targets and non-targets among the mRNAs predicted to base pair with Hfq-binding sRNAs is poorly understood. Using the Hfq-binding sRNA Spot 42 of Escherichia coli as a model, we found that predictions using only the three unstructured regions of Spot 42 substantially improved the identification of previously known and novel Spot 42 targets. Furthermore, increasing the extent of base-pairing in single or multiple base-pairing regions improved the strength of regulation, but only for the unstructured regions of Spot 42. We also found that non-targets predicted to base pair with Spot 42 lacked an Hfq-binding site, folded into a secondary structure that occluded the Spot 42 targeting site, or had overlapping Hfq-binding and targeting sites. By modifying these features, we could impart Spot 42 regulation on non-target mRNAs. Our results thus provide valuable insights into the requirements for target selection by sRNAs. The EMBO Journal (2012) 31, 1961-1974. doi:10.1038/emboj.2012.52; Published online 2 March 2012 Subject Categories: RNA
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页码:1961 / 1974
页数:14
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