iCLIP reveals the function of hnRNP particles in splicing at individual nucleotide resolution

J König, K Zarnack, G Rot, T Curk, M Kayikci… - Nature structural & …, 2010 - nature.com
J König, K Zarnack, G Rot, T Curk, M Kayikci, B Zupan, DJ Turner, NM Luscombe, J Ule
Nature structural & molecular biology, 2010nature.com
In the nucleus of eukaryotic cells, nascent transcripts are associated with heterogeneous
nuclear ribonucleoprotein (hnRNP) particles that are nucleated by hnRNP C. Despite their
abundance, however, it remained unclear whether these particles control pre-mRNA
processing. Here, we developed individual-nucleotide resolution UV cross-linking and
immunoprecipitation (iCLIP) to study the role of hnRNP C in splicing regulation. iCLIP data
show that hnRNP C recognizes uridine tracts with a defined long-range spacing consistent …
Abstract
In the nucleus of eukaryotic cells, nascent transcripts are associated with heterogeneous nuclear ribonucleoprotein (hnRNP) particles that are nucleated by hnRNP C. Despite their abundance, however, it remained unclear whether these particles control pre-mRNA processing. Here, we developed individual-nucleotide resolution UV cross-linking and immunoprecipitation (iCLIP) to study the role of hnRNP C in splicing regulation. iCLIP data show that hnRNP C recognizes uridine tracts with a defined long-range spacing consistent with hnRNP particle organization. hnRNP particles assemble on both introns and exons but remain generally excluded from splice sites. Integration of transcriptome-wide iCLIP data and alternative splicing profiles into an 'RNA map' indicates how the positioning of hnRNP particles determines their effect on the inclusion of alternative exons. The ability of high-resolution iCLIP data to provide insights into the mechanism of this regulation holds promise for studies of other higher-order ribonucleoprotein complexes.
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