Park Su Jung, Jung Hyun Ju, Nguyen Dinh Sy, Kang Hunseung
a Department of Plant Biotechnology , College of Agriculture and Life Sciences, Chonnam National University , Yongbong-dong, Buk-gu, Gwangju , South Korea.
RNA Biol. 2016 Jul 2;13(7):670-9. doi: 10.1080/15476286.2016.1191736. Epub 2016 May 27.
Although seven proteins unique to U12 intron-specific minor spliceosomes, denoted as U11/U12-65K, -59K, -48K, -35K, -31K, -25K, and -20K, have been identified in humans and the roles of some of them have been demonstrated, the functional role of most of these proteins in plants is not understood. A recent study demonstrated that Arabidopsis U11/U12-65K is essential for U12 intron splicing and normal plant development. However, the structural features and sequence motifs important for 65 K binding to U12 snRNA and other spliceosomal proteins remain unclear. Here, we demonstrated by domain-deletion analysis that the C-terminal region of the 65 K protein bound specifically to the stem-loop III of U12 snRNA, whereas the N-terminal region of the 65 K protein was responsible for interacting with the 59 K protein. Analysis of the interactions between each snRNP protein using yeast two-hybrid analysis and in planta bimolecular fluorescence complementation and luciferase complementation imaging assays demonstrated that the core interactions among the 65 K, 59 K, and 48 K proteins were conserved between plants and animals, and multiple interactions were observed among the U11/U12-snRNP proteins. Taken together, these results reveal that U11/U12-65K is an indispensible component of the minor spliceosome complex by binding to both U11/U12-59K and U12 snRNA, and that multiple interactions among the U11/U12-snRNP proteins are necessary for minor spliceosome assembly.
尽管在人类中已鉴定出7种U12内含子特异性小剪接体特有的蛋白质,分别为U11/U12 - 65K、- 59K、- 48K、- 35K、- 31K、- 25K和- 20K,并且其中一些蛋白质的作用已得到证实,但这些蛋白质在植物中的大多数功能作用尚不清楚。最近一项研究表明,拟南芥U11/U12 - 65K对于U12内含子剪接和正常植物发育至关重要。然而,65K与U12 snRNA及其他剪接体蛋白结合的重要结构特征和序列基序仍不清楚。在此,我们通过结构域缺失分析表明,65K蛋白的C末端区域特异性结合U12 snRNA的茎环III,而65K蛋白的N末端区域负责与59K蛋白相互作用。利用酵母双杂交分析以及植物体内双分子荧光互补和荧光素酶互补成像分析对每个snRNP蛋白之间的相互作用进行分析,结果表明65K、59K和48K蛋白之间的核心相互作用在植物和动物之间是保守的,并且在U11/U12 - snRNP蛋白之间观察到多种相互作用。综上所述,这些结果表明U11/U12 - 65K通过与U11/U12 - 59K和U12 snRNA结合,是小剪接体复合物不可或缺的组成部分,并且U11/U12 - snRNP蛋白之间的多种相互作用对于小剪接体组装是必要的。