Wang Jinhua, Smith Philip J, Krainer Adrian R, Zhang Michael Q
Cold Spring Harbor Laboratory, 1 Bungtown Road, Cold Spring Harbor, NY 11724, USA.
Nucleic Acids Res. 2005 Sep 7;33(16):5053-62. doi: 10.1093/nar/gki810. Print 2005.
Exonic splicing enhancers (ESEs) are pre-mRNA cis-acting elements required for splice-site recognition. We previously developed a web-based program called ESEfinder that scores any sequence for the presence of ESE motifs recognized by the human SR proteins SF2/ASF, SRp40, SRp55 and SC35 (http://rulai.cshl.edu/tools/ESE/). Using ESEfinder, we have undertaken a large-scale analysis of ESE motif distribution in human protein-coding genes. Significantly higher frequencies of ESE motifs were observed in constitutive internal protein-coding exons, compared with both their flanking intronic regions and with pseudo exons. Statistical analysis of ESE motif frequency distributions revealed a complex relationship between splice-site strength and increased or decreased frequencies of particular SR protein motifs. Comparison of constitutively and alternatively spliced exons demonstrated slightly weaker splice-site scores, as well as significantly fewer ESE motifs, in the alternatively spliced group. Our results underline the importance of ESE-mediated SR protein function in the process of exon definition, in the context of both constitutive splicing and regulated alternative splicing.
外显子剪接增强子(ESEs)是前体mRNA剪接位点识别所需的顺式作用元件。我们之前开发了一个名为ESEfinder的基于网络的程序,该程序可对任何序列进行评分,以确定其是否存在被人类SR蛋白SF2/ASF、SRp40、SRp55和SC35识别的ESE基序(http://rulai.cshl.edu/tools/ESE/)。利用ESEfinder,我们对人类蛋白质编码基因中的ESE基序分布进行了大规模分析。与侧翼内含子区域和假外显子相比,在组成型内部蛋白质编码外显子中观察到ESE基序的频率显著更高。对ESE基序频率分布的统计分析揭示了剪接位点强度与特定SR蛋白基序频率增加或减少之间的复杂关系。组成型剪接外显子和可变剪接外显子的比较表明,可变剪接组中的剪接位点得分略弱,ESE基序也明显较少。我们的结果强调了在组成型剪接和受调控的可变剪接背景下,ESE介导的SR蛋白功能在外显子定义过程中的重要性。