Park Juw Won, Jung Sungbo, Rouchka Eric C, Tseng Yu-Ting, Xing Yi
Department of Computer Engineering and Computer Science, University of Louisville, Louisville, KY 40292, USA KBRIN Bioinformatics Core, University of Louisville, Louisville, KY 40202, USA Department of Microbiology, Immunology & Molecular Genetics, University of California, Los Angeles, CA 90095, USA
Department of Computer Engineering and Computer Science, University of Louisville, Louisville, KY 40292, USA.
Nucleic Acids Res. 2016 Jul 8;44(W1):W333-8. doi: 10.1093/nar/gkw410. Epub 2016 May 12.
RNA-binding proteins (RBPs) play a critical role in the regulation of alternative splicing (AS), a prevalent mechanism for generating transcriptomic and proteomic diversity in eukaryotic cells. Studies have shown that AS can be regulated by RBPs in a binding-site-position dependent manner. Depending on where RBPs bind, splicing of an alternative exon can be enhanced or suppressed. Therefore, spatial analyses of RBP motifs and binding sites around alternative exons will help elucidate splicing regulation by RBPs. The development of high-throughput sequencing technologies has allowed transcriptome-wide analyses of AS and RBP-RNA interactions. Given a set of differentially regulated alternative exons obtained from RNA sequencing (RNA-seq) experiments, the rMAPS web server (http://rmaps.cecsresearch.org) performs motif analyses of RBPs in the vicinity of alternatively spliced exons and creates RNA maps that depict the spatial patterns of RBP motifs. Similarly, rMAPS can also perform spatial analyses of RBP-RNA binding sites identified by cross-linking immunoprecipitation sequencing (CLIP-seq) experiments. We anticipate rMAPS will be a useful tool for elucidating RBP regulation of alternative exon splicing using high-throughput sequencing data.
RNA结合蛋白(RBPs)在可变剪接(AS)的调控中起着关键作用,可变剪接是真核细胞中产生转录组和蛋白质组多样性的一种普遍机制。研究表明,可变剪接可由RNA结合蛋白以依赖于结合位点位置的方式进行调控。根据RNA结合蛋白的结合位置,可变外显子的剪接可被增强或抑制。因此,对可变外显子周围RNA结合蛋白基序和结合位点进行空间分析,将有助于阐明RNA结合蛋白对剪接的调控机制。高通量测序技术的发展使得对可变剪接和RNA结合蛋白-RNA相互作用进行全转录组分析成为可能。给定一组从RNA测序(RNA-seq)实验中获得的差异调控可变外显子,rMAPS网络服务器(http://rmaps.cecsresearch.org)可对可变剪接外显子附近的RNA结合蛋白进行基序分析,并创建描绘RNA结合蛋白基序空间模式的RNA图谱。同样,rMAPS也可以对通过交联免疫沉淀测序(CLIP-seq)实验鉴定出的RNA结合蛋白-RNA结合位点进行空间分析。我们预计rMAPS将成为利用高通量测序数据阐明RNA结合蛋白对可变外显子剪接调控机制的有用工具。