Masuyama Kaoru, Taniguchi Ichiro, Okawa Katsuya, Ohno Mutsuhito
Institute for Virus Research, Kyoto University, Kyoto 606-8507, Japan and CREST, JST, Japan.
Biochem Biophys Res Commun. 2007 Aug 3;359(3):580-5. doi: 10.1016/j.bbrc.2007.05.144. Epub 2007 May 30.
Purine-rich exonic splicing enhancers (ESEs) stimulate splicing of the adjacent introns with suboptimal splice sites. To elucidate the mechanism regarding ESEs, factors specifically associated with ESEs in HeLa cell nuclear extracts were previously investigated, and shown to include SR (serine/arginine-rich) proteins. However, factors associated with ESEs in vivo have not yet been explored. Here we show that a GAA repeat RNA sequence, a typical ESE, is associated in Xenopus oocyte nuclei with at least one SR protein, SF2/ASF, as was expected. Moreover, components of SF3a/b complexes, U2 snRNA, and U2AF(65) were also found to be associated with the ESE in the nucleus. Since SF3a/b complexes are the constituents of the 17S U2 snRNP, these results suggest that the 17S U2 snRNP is associated with the ESE in the nucleus, probably through bridging interactions of U2AF and SR proteins. The identified factors may represent a functional splicing enhancer complex in vivo.
富含嘌呤的外显子剪接增强子(ESEs)可刺激具有次优剪接位点的相邻内含子的剪接。为阐明ESEs的作用机制,此前研究了HeLa细胞核提取物中与ESEs特异性相关的因子,结果表明其中包括SR(富含丝氨酸/精氨酸)蛋白。然而,尚未对体内与ESEs相关的因子进行探索。在此我们发现,如预期的那样,典型的ESE——GAA重复RNA序列在非洲爪蟾卵母细胞核中与至少一种SR蛋白SF2/ASF相关联。此外,还发现SF3a/b复合物的组分、U2 snRNA和U2AF(65)也在细胞核中与该ESE相关联。由于SF3a/b复合物是17S U2 snRNP的组成部分,这些结果表明17S U2 snRNP在细胞核中与ESE相关联,可能是通过U2AF和SR蛋白的桥接相互作用。所鉴定的这些因子可能代表了体内一种功能性的剪接增强子复合物。