| Literature DB >> 25574948 |
Nan Liu1, Guoqing Niu1, Zhoujie Xie1, Zhiyun Chen1, Andreas Itzek1, Jens Kreth2, Allison Gillaspy1, Lin Zeng3, Robert Burne3, Fengxia Qi2, Justin Merritt4.
Abstract
In both prokaryotes and eukaryotes, insight into gene function is typically obtained by in silico homology searches and/or phenotypic analyses of strains bearing mutations within open reading frames. However, the studies herein illustrate how mRNA function is not limited to the expression of a cognate protein. We demonstrate that a stress-induced protein-encoding mRNA (irvA) from the dental caries pathogen Streptococcus mutans directly modulates target mRNA (gbpC) stability through seed pairing interactions. The 5' untranslated region of irvA mRNA is a trans riboregulator of gbpC and a critical activator of the DDAG stress response, whereas IrvA functions independently in the regulation of natural competence. The irvA riboregulatory domain controls GbpC production by forming irvA-gbpC hybrid mRNA duplexes that prevent gbpC degradation by an RNase J2-mediated pathway. These studies implicate a potentially ubiquitous role for typical protein-encoding mRNAs as riboregulators, which could alter current concepts in gene regulation.Entities:
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Year: 2015 PMID: 25574948 PMCID: PMC5663275 DOI: 10.1016/j.molcel.2014.11.003
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970