Brosi R, Hauri H P, Krämer A
Département de Biologie Cellulaire, Sciences III, Université de Genève, Switzerland.
J Biol Chem. 1993 Aug 15;268(23):17640-6.
Components required for the splicing of nuclear messenger RNA precursors in vitro have been isolated from HeLa cells. Here we describe the separation of splicing factor SF3 into two components, SF3a and SF3b. Both activities are required together with several other protein factors and U1 and U2 small nuclear ribonucleoproteins for the assembly of a presplicing complex which represents the first ATP-dependent step in the assembly of the active spliceosome. SF3a has been purified to homogeneity by a combination of ion-exchange chromatography, gel filtration, and glycerol gradient sedimentation. It consists of a complex of three polypeptides of 60, 66, and 120 kDa. The association of SF3a activity with these polypeptides has been confirmed by immunoprecipitation and depletion experiments using a monoclonal antibody directed against the 66-kDa subunit.
用于体外剪接细胞核信使RNA前体所需的成分已从HeLa细胞中分离出来。在此我们描述了剪接因子SF3分离为两个成分,即SF3a和SF3b。这两种活性与其他几种蛋白质因子以及U1和U2小核核糖核蛋白一起,是组装前体剪接复合物所必需的,该复合物代表活性剪接体组装过程中第一个依赖ATP的步骤。通过离子交换色谱、凝胶过滤和甘油梯度沉降相结合的方法,已将SF3a纯化至同质。它由60 kDa、66 kDa和120 kDa的三种多肽组成的复合物。使用针对66 kDa亚基的单克隆抗体进行的免疫沉淀和去除实验已证实SF3a活性与这些多肽相关。