Miyakoshi Masatoshi, Chao Yanjie, Vogel Jörg
RNA Biology Group, Institute for Molecular Infection Biology University of Würzburg, Würzburg, Germany.
RNA Biology Group, Institute for Molecular Infection Biology University of Würzburg, Würzburg, Germany
EMBO J. 2015 Jun 3;34(11):1478-92. doi: 10.15252/embj.201490546. Epub 2015 Jan 28.
There is an expanding list of examples by which one mRNA can posttranscriptionally influence the expression of others. This can involve RNA sponges that sequester regulatory RNAs of mRNAs in the same regulon, but the underlying molecular mechanism of such mRNA cross talk remains little understood. Here, we report sponge-mediated mRNA cross talk in the posttranscriptional network of GcvB, a conserved Hfq-dependent small RNA with one of the largest regulons known in bacteria. We show that mRNA decay from the gltIJKL locus encoding an amino acid ABC transporter generates a stable fragment (SroC) that base-pairs with GcvB. This interaction triggers the degradation of GcvB by RNase E, alleviating the GcvB-mediated mRNA repression of other amino acid-related transport and metabolic genes. Intriguingly, since the gltIJKL mRNA itself is a target of GcvB, the SroC sponge seems to enable both an internal feed-forward loop to activate its parental mRNA in cis and activation of many trans-encoded mRNAs in the same pathway. Disabling this mRNA cross talk affects bacterial growth when peptides are the sole carbon and nitrogen sources.
越来越多的例子表明,一种信使核糖核酸(mRNA)可以在转录后影响其他mRNA的表达。这可能涉及到RNA海绵,它能隔离同一调控子中mRNA的调控RNA,但这种mRNA相互作用的潜在分子机制仍知之甚少。在这里,我们报道了在GcvB的转录后网络中海绵介导的mRNA相互作用,GcvB是一种保守的、依赖于Hfq的小RNA,其调控子是细菌中已知最大的调控子之一。我们表明,编码氨基酸ABC转运蛋白的gltIJKL基因座的mRNA衰变产生了一个与GcvB碱基配对的稳定片段(SroC)。这种相互作用触发了核糖核酸酶E对GcvB的降解,减轻了GcvB介导的对其他氨基酸相关转运和代谢基因的mRNA抑制。有趣的是,由于gltIJKL mRNA本身是GcvB的靶标,SroC海绵似乎既能使一个内部前馈环顺式激活其亲本mRNA,又能激活同一途径中的许多反式编码mRNA。当肽是唯一的碳源和氮源时,禁用这种mRNA相互作用会影响细菌生长。