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二级结构是酵母 3' 剪接位点识别所必需的。

Secondary structure is required for 3' splice site recognition in yeast.

机构信息

Department of Cell Biology, Faculty of Science, Charles University in Prague, Prague, Czech Republic.

出版信息

Nucleic Acids Res. 2011 Dec;39(22):9759-67. doi: 10.1093/nar/gkr662. Epub 2011 Sep 5.

Abstract

Higher order RNA structures can mask splicing signals, loop out exons, or constitute riboswitches all of which contributes to the complexity of splicing regulation. We identified a G to A substitution between branch point (BP) and 3' splice site (3'ss) of Saccharomyces cerevisiae COF1 intron, which dramatically impaired its splicing. RNA structure prediction and in-line probing showed that this mutation disrupted a stem in the BP-3'ss region. Analyses of various COF1 intron modifications revealed that the secondary structure brought about the reduction of BP to 3'ss distance and masked potential 3'ss. We demonstrated the same structural requisite for the splicing of UBC13 intron. Moreover, RNAfold predicted stable structures for almost all distant BP introns in S. cerevisiae and for selected examples in several other Saccharomycotina species. The employment of intramolecular structure to localize 3'ss for the second splicing step suggests the existence of pre-mRNA structure-based mechanism of 3'ss recognition.

摘要

高等 RNA 结构可以掩盖剪接信号、环出外显子或构成核酶,所有这些都增加了剪接调控的复杂性。我们在酿酒酵母 COF1 内含子的分支点 (BP) 和 3' 剪接位点 (3'ss) 之间发现了一个 G 到 A 的取代,这极大地损害了它的剪接。RNA 结构预测和在线探测表明,该突变破坏了 BP-3'ss 区域的一个茎。对各种 COF1 内含子修饰的分析表明,二级结构导致 BP 到 3'ss 距离的缩短,并掩盖了潜在的 3'ss。我们证明了 UBC13 内含子剪接也存在相同的结构要求。此外,RNAfold 预测了酿酒酵母中几乎所有远距离 BP 内含子以及其他几种 Saccharomycotina 物种中选定例子的稳定结构。第二个剪接步骤中利用分子内结构来定位 3'ss,表明存在基于前体 mRNA 结构的 3'ss 识别机制。

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