Krämer A, Utans U
University of Basel, Department of Cell Biology, Switzerland.
EMBO J. 1991 Jun;10(6):1503-9. doi: 10.1002/j.1460-2075.1991.tb07670.x.
The splicing of nuclear messenger RNA precursors can be reproduced in vitro with fractions obtained after chromatography of HeLa cell nuclear extracts. Here we report the chromatographic separation of three protein factors: SF1, SF3 and U2AF. All factors function early in the splicing reaction, in the assembly of a pre-splicing complex. Likewise, all factors are essential for the production of spliced RNA. In addition to their distinct chromatographic properties, the splicing factors can be distinguished by their sensitivities to heat and N-ethylmaleimide. All activities can be detected in a cytoplasmic A-100 fraction from HeLa cells. The fact that SF1, SF3 and U2AF are essential factors in pre-splicing complex formation raises the possibility that SF1 and/or SF3 participate in the interaction of U2 snRNP with the branch point in addition to U2AF.
利用从HeLa细胞核提取物经色谱分离得到的组分,可在体外重现核信使RNA前体的剪接过程。在此,我们报告了三种蛋白质因子的色谱分离:SF1、SF3和U2AF。所有这些因子在剪接反应早期、在前剪接复合体的组装过程中发挥作用。同样,所有因子对于剪接RNA的产生都是必不可少的。除了其独特的色谱性质外,这些剪接因子还可通过它们对热和N-乙基马来酰亚胺的敏感性加以区分。在HeLa细胞的细胞质A-100组分中可检测到所有活性。SF1、SF3和U2AF是前剪接复合体形成中的必需因子,这一事实增加了一种可能性,即除了U2AF外,SF1和/或SF3还参与U2 snRNP与分支点的相互作用。