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人类剪接因子ASF/SF2的第二个RNA结合结构域是控制腺病毒E1A 5'端可变剪接位点选择的关键结构域。

The second RNA-binding domain of the human splicing factor ASF/SF2 is the critical domain controlling adenovirus E1A alternative 5'-splice site selection.

作者信息

Dauksaite Vita, Akusjärvi Göran

机构信息

Department of Medical Biochemistry and Microbiology, Uppsala University, BMC, Box 582, 751 23 Uppsala, Sweden.

出版信息

Biochem J. 2004 Jul 15;381(Pt 2):343-50. doi: 10.1042/BJ20040408.

Abstract

The human splicing factor ASF/SF2 (alternative splicing factor/splicing factor 2) is modular in structure with two RNA-binding domains (RBD1 and RBD2) and a C-terminal domain rich in arginine-serine dipeptide repeats. ASF/SF2 is an essential splicing factor that also functions as an important regulator of alternative splicing. In adenovirus E1A (early region 1A) alternative pre-mRNA splicing, ASF/SF2 functions as a strong inducer of proximal 5'-splice-site selection, both in vitro and in vivo. In the present study, we tested the functional role of individual domains of ASF/SF2 in alternative splicing in vitro. We show that ASF/SF2-RBD2 is the critical domain controlling E1A alternative splicing. In fact, RBD2 alone is sufficient to mimic the activity of the full-length ASF/SF2 protein as an inducer of proximal 5'-splice-site selection in vitro. The RBD2 domain induces a switch to E1A-proximal 5'-splice-site usage by repressing distal 12 S splicing and simultaneously stimulates proximal 13 S splicing. In contrast, the ASF/SF2-RBD1 domain has a more general splicing enhancer phenotype and appears to stimulate preferentially cap-proximal 5'-splice-site selection. Furthermore, the SWQDLKD motif, which is conserved in all SR proteins (serine/arginine-rich proteins) containing two RBDs, and the ribonucleoprotein-1-type RNA recognition motif were both found to be necessary for the alternative splice-site-switching activity of ASF/SF2. The RNP-1 motif was necessary for efficient RNA binding, whereas the SWQDLKD motif most probably contributes by functioning as a surface-mediating critical protein-protein contact during spliceosome assembly.

摘要

人类剪接因子ASF/SF2(可变剪接因子/剪接因子2)结构呈模块化,具有两个RNA结合结构域(RBD1和RBD2)以及一个富含精氨酸 - 丝氨酸二肽重复序列的C末端结构域。ASF/SF2是一种必需的剪接因子,同时也是可变剪接的重要调节因子。在腺病毒E1A(早期区域1A)可变前体mRNA剪接中,ASF/SF2在体外和体内均作为近端5'剪接位点选择的强诱导剂发挥作用。在本研究中,我们在体外测试了ASF/SF2各个结构域在可变剪接中的功能作用。我们发现ASF/SF2 - RBD2是控制E1A可变剪接的关键结构域。事实上,单独的RBD2就足以模拟全长ASF/SF2蛋白在体外作为近端5'剪接位点选择诱导剂的活性。RBD2结构域通过抑制远端12S剪接并同时刺激近端13S剪接,诱导向E1A近端5'剪接位点使用的转变。相比之下,ASF/SF2 - RBD1结构域具有更普遍的剪接增强子表型,似乎优先刺激帽近端5'剪接位点的选择。此外,在所有含有两个RBD的SR蛋白(富含丝氨酸/精氨酸的蛋白)中保守的SWQDLKD基序以及核糖核蛋白1型RNA识别基序,对于ASF/SF2的可变剪接位点转换活性都是必需的。RNP - 1基序对于有效的RNA结合是必需的,而SWQDLKD基序很可能通过在剪接体组装过程中作为介导关键蛋白质 - 蛋白质接触的表面发挥作用。

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