Damianov Andrey, Schreiner Silke, Bindereif Albrecht
Institut für Biochemie, Justus-Liebig-Universität Giessen, D-35392 Giessen, Germany.
Mol Cell Biol. 2004 Feb;24(4):1700-8. doi: 10.1128/MCB.24.4.1700-1708.2004.
U12-dependent introns are spliced by the so-called minor spliceosome, requiring the U11, U12, and U4atac/U6atac snRNPs in addition to the U5 snRNP. We have recently identified U6-p110 (SART3) as a novel human recycling factor that is related to the yeast splicing factor Prp24. U6-p110 transiently associates with the U6 and U4/U6 snRNPs during the spliceosome cycle, regenerating functional U4/U6 snRNPs from singular U4 and U6 snRNPs. Here we investigated the involvement of U6-p110 in recycling of the U4atac/U6atac snRNP. In contrast to the major U6 and U4/U6 snRNPs, p110 is primarily associated with the U6atac snRNP but is almost undetectable in the U4atac/U6atac snRNP. Since p110 does not occur in U5 snRNA-containing complexes, it appears to be transiently associated with U6atac during the cycle of the minor spliceosome. The p110 binding site was mapped to U6 nucleotides 38 to 57 and U6atac nucleotides 10 to 30, which are highly conserved between these two functionally related snRNAs. With a U12-dependent in vitro splicing system, we demonstrate that p110 is required for recycling of the U4atac/U6atac snRNP.
依赖U12的内含子由所谓的次要剪接体进行剪接,除U5 snRNP外,还需要U11、U12和U4atac/U6atac snRNP。我们最近鉴定出U6-p110(SART3)是一种新型的人类循环因子,它与酵母剪接因子Prp24相关。在剪接体循环过程中,U6-p110与U6和U4/U6 snRNP短暂结合,从单个的U4和U6 snRNP再生出功能性的U4/U6 snRNP。在此,我们研究了U6-p110在U4atac/U6atac snRNP循环中的作用。与主要的U6和U4/U6 snRNP不同,p110主要与U6atac snRNP结合,但在U4atac/U6atac snRNP中几乎检测不到。由于p110不存在于含U5 snRNA的复合物中,它似乎在次要剪接体循环过程中与U6atac短暂结合。p110结合位点被定位到U6的38至57位核苷酸以及U6atac的10至30位核苷酸,这两个功能相关的snRNA之间高度保守。利用依赖U12的体外剪接系统,我们证明p110是U4atac/U6atac snRNP循环所必需的。