![]() Additional sequence elements can recruit regulatory RNA-binding proteins either to enhance or silence splice site recognition depending on their position relative to the splice sites. These core splice site motifs, however, contain only about half of the information required to define exon/intron boundaries. U1 and U2 snRNPs recognise the core motifs present at the 5′ and 3′ splice sites, respectively. Pre-mRNA splicing is catalysed by small nuclear ribonucleoprotein particles (snRNP) that recognise the splice sites on pre-mRNA and remove the introns with great precision. Small nuclear ribonucleoprotein particles TIA1, Individual-nucleotide resolution UV-crosslinking and immunoprecipitation KD, Individual-nucleotide resolution UV-crosslinking and affinity purification iCLIP, The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.Ĭompeting interests: The authors have declared that no competing interests exist. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.įunding: This work was supported by Medical Research Council (MRC, European Research Council (ERC,, 206726-CLIP), Human Frontier Science Program (HFSP, RGP0024/2008-C), and Slovenian Research Agency (P2-0209, J2-2197, L2-1112, Z7-3665). Received: ApAccepted: SeptemPublished: October 26, 2010Ĭopyright: © 2010 Wang et al. PLoS Biol 8(10):Īcademic Editor: Tom Misteli, National Cancer Institute, United States of America (2010) iCLIP Predicts the Dual Splicing Effects of TIA-RNA Interactions. These findings highlight the importance of analysing distal regulatory sites in order to fully understand the regulation of alternative splicing.Ĭitation: Wang Z, Kayikci M, Briese M, Zarnack K, Luscombe NM, Rot G, et al. This result suggests that alternative splicing is affected by the timing of alternative exon definition relative to the recognition of the preceding 5′ splice site. In particular, we show that TIA proteins can regulate distal alternative 3′ splice sites by binding at the 5′ splice site of the preceding exon. The identified binding positions successfully predict the local enhancing and distal silencing effects of TIA proteins. Here, we use a new method to map the positions of TIA-RNA interactions with high resolution on a transcriptome-wide scale. The TIA proteins are key splicing regulators that enhance the recognition of 5′ splice sites, and their distal effects have remained unexplored so far. Recently, it has been suggested that splicing of alternative exons can also be regulated by distal regulatory sites, but the underlying mechanism is not clear. Studies of splicing regulation have generally focused on RNA elements located close to alternative exons. Thus, our findings indicate that changes in splicing kinetics could mediate the distal regulation of alternative splicing. These data are consistent with a model where TIA proteins shorten the time available for definition of an alternative exon by enhancing recognition of the preceding 5′ splice site. Using transcriptome-wide high-resolution mapping of TIA-RNA interactions we evaluated the distal splicing effects of TIA proteins. Surprisingly, TIA binding at 5′ splice sites silenced distal cassette and variable-length exons without binding in proximity to the regulated alternative 3′ splice sites. The predictions were validated in an unbiased manner using splice-junction microarrays, RT-PCR, and minigene constructs, which showed that TIA proteins maintain splicing fidelity and regulate alternative splicing by binding exclusively downstream of 5′ splice sites. Binding downstream of 5′ splice sites was used to predict the effects of TIA proteins in enhancing inclusion of proximal exons and silencing inclusion of distal exons. ![]() We used UV-crosslinking and immunoprecipitation (iCLIP) to find that TIA1 and TIAL1 bind at the same positions on human RNAs. ![]() ![]() However, effects of TIA proteins on splicing of distal exons have not yet been explored. T-cell intracellular antigen 1 (TIA1) and TIA1-like 1 (TIAL1) locally enhance exon inclusion by recruiting U1 snRNP to 5′ splice sites. The regulation of alternative splicing involves interactions between RNA-binding proteins and pre-mRNA positions close to the splice sites. ![]()
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