Pikielny C W, Bindereif A, Green M R
Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, Massachusetts 02138.
Genes Dev. 1989 Apr;3(4):479-87. doi: 10.1101/gad.3.4.479.
We have reconstituted in vitro the four snRNPs known to be involved in pre-mRNA splicing: U1, U2, U5, and U4/6. Reconstitution involves adding either authentic or in vitro-synthesized snRNAs to extracts enriched in snRNP structural polypeptides. The reconstituted snRNPs have the same buoyant density and are immunoprecipitated by the same antibodies as authentic snRNPs. Thus, the polypeptide composition of reconstituted snRNPs is similar, if not identical, to that of authentic snRNPs. We show further that a reconstituted U4/U6 particle is fully functional in forming splicing complexes with pre-mRNA. As is the case for the authentic U4/U6 snRNP, the reconstituted U4 snRNP, but not the U6 snRNA, dissociates from the complex prior to formation of the mature spliceosome. The ability to reconstitute snRNPs and assay their activity in spliceosome formation should provide a powerful approach to study these particles.
我们已经在体外重组了已知参与前体mRNA剪接的四种小核核糖核蛋白颗粒(snRNP):U1、U2、U5和U4/6。重组过程包括将真实的或体外合成的snRNA添加到富含snRNP结构多肽的提取物中。重组后的snRNP具有相同的浮力密度,并且能被与真实snRNP相同的抗体免疫沉淀。因此,重组snRNP的多肽组成即便不完全相同,也与真实snRNP相似。我们进一步表明,重组的U4/U6颗粒在与前体mRNA形成剪接复合物方面完全具备功能。与真实的U4/U6 snRNP情况一样,重组的U4 snRNP,而非U6 snRNA,在成熟剪接体形成之前从复合物中解离。重组snRNP并检测它们在剪接体形成中的活性的能力,应该为研究这些颗粒提供一种强有力的方法。