Department of Biology, Graduate School of Science, Kobe University, Nadaku, Kobe, Japan.
RNA Biol. 2009 Sep-Oct;6(4):395-8. doi: 10.4161/rna.6.4.9318. Epub 2009 Sep 21.
In metazoan organisms, alternative splicing is a central mechanism for the regulation of gene expression. However, many questions remain about the underlying molecular mechanisms. Our recent work suggests that U1 snRNP-independent premRNA splicing occurs in humans, which contributes to the regulation of alternative splicing. So far it has been reported that several pre-mRNAs were spliced efficiently in a U1 snRNP-independent manner in vitro. Although the molecular mechanism and functional significance of U1-independent pre-mRNA splicing are not well understood, a model of how the 5' splice site is recognized U1-independently has been proposed. In this review, we first overview a model in which the 5' splice site is recognized by SR proteins and U6 snRNA. We then discuss our novel model and the functional significance of U1-independent pre-mRNA splicing in the regulation of alternative splicing, based on our recent work.
在后生动物生物中,选择性剪接是基因表达调控的一种主要机制。然而,许多关于潜在分子机制的问题仍然存在。我们最近的工作表明,非依赖 U1 小核核糖核蛋白的前体 RNA 剪接发生在人类中,这有助于调节选择性剪接。到目前为止,已经有报道称,在体外,几种前体 RNA 能够以非依赖 U1 小核核糖核蛋白的方式有效地进行剪接。尽管非依赖 U1 的前体 RNA 剪接的分子机制和功能意义尚不清楚,但已经提出了一种模型,即 5' 剪接位点如何非依赖 U1 被识别。在这篇综述中,我们首先概述了一种模型,即 5' 剪接位点被 SR 蛋白和 U6 snRNA 识别。然后,我们根据我们最近的工作,讨论了我们的新模型以及非依赖 U1 的前体 RNA 剪接在调节选择性剪接中的功能意义。