Center for RNA Molecular Biology, Case Western Reserve University, Cleveland, OH, USA.
RNA Biol. 2010 May-Jun;7(3):345-53. doi: 10.4161/rna.7.3.12089. Epub 2010 May 16.
The spliceosome, the ribonucleoprotein assembly that removes the intervening sequences from pre-mRNAs through splicing, is one of the most complex cellular machines. In humans it is composed of -150 proteins and five RNAs (snRNAs). One of the snRNAs, U6, contains sequences analogous to all the RNA elements that form the active site of the group II introns, ribozymes that perform a splicing reaction mechanistically identical to spliceosomal splicing. Interestingly, U6 is the only snRNA that is indispensable for splicing and in vitro, in complex with another snRNA, it can catalyze a primordial splicing reaction in the absence of all other spliceosomal factors. On the other hand, discovery of an RNase H-like domain in a spliceosomal protein that is closely associated with splice sites suggests that proteins may be involved in formation of the active site. Thus, whether the spliceosome is an RNA or RNA-protein catalyst remains uncertain.
剪接体是一种核糖核蛋白复合物,通过剪接从 pre-mRNA 中去除内含子序列,是最复杂的细胞机器之一。在人类中,它由 150 多种蛋白质和 5 种 RNA(snRNA)组成。其中一种 snRNA,U6,包含与所有形成 II 组内含子活性位点的 RNA 元件类似的序列,这些核酶通过与剪接体剪接机制相同的剪接反应进行催化。有趣的是,U6 是剪接所必需的唯一 snRNA,并且在体外与另一种 snRNA 形成复合物时,它可以在没有其他剪接体因子的情况下催化原始剪接反应。另一方面,在与剪接位点密切相关的剪接体蛋白中发现了一种 RNase H 样结构域,这表明蛋白质可能参与活性位点的形成。因此,剪接体是 RNA 还是 RNA-蛋白催化剂仍然不确定。