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Characterization of cis-acting elements that control oscillating alternative splicing

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Version 2 2018-09-28, 12:58
Version 1 2018-09-11, 00:24
journal contribution
posted on 2018-09-28, 12:58 authored by Gesine Goldammer, Alexander Neumann, Miriam Strauch, Michaela Müller-McNicoll, Florian Heyd, Marco Preußner

Alternative splicing (AS) in response to changing external conditions often requires alterations in the ability of sequence-specific RNA-binding proteins to bind to cis-acting sequences in their target pre-mRNA. While daily oscillations in AS events have been described in several organisms, cis-acting sequences that control time of the day-dependent AS remain largely elusive. Here we define cis-regulatory RNA elements that control body-temperature driven rhythmic AS using the mouse U2af26 gene as a model system. We identify a complex network of cis-regulatory sequences that regulate AS of U2af26, and show that the activity of two enhancer elements is necessary for oscillating AS. A minigene comprising these U2af26 regions recapitulates rhythmic splicing of the endogenous gene, which is controlled through temperature-regulated SR protein phosphorylation. Mutagenesis of the minigene delineates the cis-acting enhancer element for SRSF2 within exon 6 to single nucleotide resolution and reveals that the combined activity of SRSF2 and SRSF7 is required for oscillating U2af26 AS. By combining RNA-Seq with an siRNA screen and individual-nucleotide resolution cross-linking and immunoprecipitation (iCLIP), we identify a complex network of SR proteins that globally controls temperature-dependent rhythmic AS, with the direction of splicing depending on the position of the cis-acting elements. Together, we provide detailed insights into the sequence requirements that allow trans-acting factors to generate daily rhythms in AS.

Funding

This work was supported by the Deutsche Forschungsgemeinschaft [HE5398/3];Deutsche Forschungsgemeinschaft [SFB958/A21];Deutsche Forschungsgemeinschaft [HE5398/4] and SFB902.

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