Characterization of cis-acting elements that control oscillating alternative splicing

RNA Biol. 2018;15(8):1081-1092. doi: 10.1080/15476286.2018.1502587. Epub 2018 Sep 10.

Abstract

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.

Keywords: Alternative splicing; SR proteins; body temperature cycle; circadian clock; iCLIP; minigene; phosphorylation; splicing network.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing*
  • Animals
  • Cells, Cultured
  • Exons
  • Mice
  • RNA Precursors / genetics*
  • RNA Precursors / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism*
  • Regulatory Sequences, Nucleic Acid*
  • Serine-Arginine Splicing Factors / genetics
  • Serine-Arginine Splicing Factors / metabolism*
  • Splicing Factor U2AF / genetics*
  • Splicing Factor U2AF / metabolism

Substances

  • RNA Precursors
  • RNA, Messenger
  • SRSF2 protein, mouse
  • Splicing Factor U2AF
  • U2af1l4 protein, mouse
  • Serine-Arginine Splicing Factors

Grants and funding

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