Cell Biology and Metabolism Program, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD, USA.
EMBO J. 2012 Apr 18;31(8):1961-74. doi: 10.1038/emboj.2012.52. Epub 2012 Mar 2.
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.
细菌中的 Hfq 结合小 RNA(sRNA)通过有限的碱基配对相互作用调节靶 mRNA 的稳定性和翻译效率。虽然这些 sRNA 被认为是作为应激反应的一部分调节众多 mRNA,但对于预测与 Hfq 结合 sRNA 碱基配对的 mRNA 中哪些是靶标,哪些是非靶标,了解甚少。我们以大肠杆菌的 Hfq 结合 sRNA Spot 42 为模型,发现仅使用 Spot 42 的三个无结构区域的预测可以显著提高先前已知和新的 Spot 42 靶标的识别。此外,增加单个或多个碱基配对区域的碱基配对程度可以增强调控强度,但仅针对 Spot 42 的无结构区域。我们还发现,预测与 Spot 42 碱基配对的非靶标缺乏 Hfq 结合位点,折叠成一种二级结构,阻断了 Spot 42 的靶标位点,或者具有重叠的 Hfq 结合和靶标位点。通过修饰这些特征,我们可以将 Spot 42 的调控赋予非靶标 mRNA。因此,我们的研究结果为 sRNA 靶标选择的要求提供了有价值的见解。