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微小RNA(miRNA)前体的结构特征及其与miRNA生物合成和小干扰RNA/短发夹RNA设计的相关性。

Structural features of microRNA (miRNA) precursors and their relevance to miRNA biogenesis and small interfering RNA/short hairpin RNA design.

作者信息

Krol Jacek, Sobczak Krzysztof, Wilczynska Urszula, Drath Maria, Jasinska Anna, Kaczynska Danuta, Krzyzosiak Wlodzimierz J

机构信息

Laboratory of Cancer Genetics, Institute of Bioorganic Chemistry, Polish Academy of Sciences, Noskowskiego 12/14, 61-704, Poznan, Poland.

出版信息

J Biol Chem. 2004 Oct 1;279(40):42230-9. doi: 10.1074/jbc.M404931200. Epub 2004 Aug 2.

Abstract

We have established the structures of 10 human microRNA (miRNA) precursors using biochemical methods. Eight of these structures turned out to be different from those that were computer-predicted. The differences localized in the terminal loop region and at the opposite side of the precursor hairpin stem. We have analyzed the features of these structures from the perspectives of miRNA biogenesis and active strand selection. We demonstrated the different thermodynamic stability profiles for pre-miRNA hairpins harboring miRNAs at their 5'- and 3'-sides and discussed their functional implications. Our results showed that miRNA prediction based on predicted precursor structures may give ambiguous results, and the success rate is significantly higher for the experimentally determined structures. On the other hand, the differences between the predicted and experimentally determined structures did not affect the stability of termini produced through "conceptual dicing." This result confirms the value of thermodynamic analysis based on mfold as a predictor of strand section by RNAi-induced silencing complex (RISC).

摘要

我们利用生化方法确定了10种人类微小RNA(miRNA)前体的结构。结果发现其中8种结构与计算机预测的不同。差异位于末端环区域以及前体发夹茎的相对侧。我们从miRNA生物合成和活性链选择的角度分析了这些结构的特征。我们展示了在其5'端和3'端含有miRNA的前体miRNA发夹具有不同的热力学稳定性概况,并讨论了它们的功能意义。我们的结果表明,基于预测的前体结构进行miRNA预测可能会得出模糊的结果,而对于实验确定的结构,成功率要高得多。另一方面,预测结构与实验确定结构之间的差异并不影响通过“概念切割”产生的末端的稳定性。这一结果证实了基于mfold的热力学分析作为RNA干扰诱导沉默复合体(RISC)对链段预测指标的价值。

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