Key result
HRP-2, the C. elegans homolog of mammalian hnRNP Q and R, binds to the UCUAUC intronic hexamer and regulates the alternative splicing of unc-52 and lin-10 genes.
Identifies HRP-2 as an alternative splicing factor in C. elegans that binds to the UCUAUC regulatory element.
Findings in C. elegans warrant caution for translation; extends splicing regulation models and leaves open hnRNP Q/R conservation in mammals.
Alternative splicing is regulated by cis sequences in the pre-mRNA that serve as binding sites for trans-acting alternative splicing factors. In a previous study, we used bioinformatics and molecular biology to identify and confirm that the intronic hexamer sequence UCUAUC is a nematode alternative splicing regulatory element. In this study, we used RNA affinity chromatography to identify trans factors that bind to this sequence. HRP-2, the Caenorhabditis elegans homolog of human heterogeneous nuclear ribonucleoproteins Q and R, binds to UCUAUC in the context of unc-52 intronic regulatory sequences as well as to RNAs containing tandem repeats of this sequence. The three Us in the hexamer are the most important determinants of this binding specificity. We demonstrate, using RNA interference, that HRP-2 regulates the alternative splicing of two genes, unc-52 and lin-10, both of which have cassette exons flanked by an intronic UCUAUC motif. We propose that HRP-2 is a protein responsible for regulating alternative splicing through binding interactions with the UCUAUC sequence.
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Kabat et al. (2009) studied this question. RNA interference of HRP-2 was evaluated on Alternative splicing of unc-52 and lin-10 genes. HRP-2, the C. elegans homolog of mammalian hnRNP Q and R, binds to the UCUAUC intronic hexamer and regulates the alternative splicing of unc-52 and lin-10 genes.
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