EWS splicing regulation contributes to balancing Foxp1 isoforms required for neuronal differentiation

Nucleic Acids Res. 2022 Apr 8;50(6):3362-3378. doi: 10.1093/nar/gkac154.

Abstract

Alternative splicing is a key regulatory process underlying the amplification of genomic information and the expansion of proteomic diversity, particularly in brain. Here, we identify the Ewing sarcoma protein (EWS) as a new player of alternative splicing regulation during neuronal differentiation. Knockdown of EWS in neuronal progenitor cells leads to premature differentiation. Transcriptome profiling of EWS-depleted cells revealed global changes in splicing regulation. Bioinformatic analyses and biochemical experiments demonstrated that EWS regulates alternative exons in a position-dependent fashion. Notably, several EWS-regulated splicing events are physiologically modulated during neuronal differentiation and EWS depletion in neuronal precursors anticipates the splicing-pattern of mature neurons. Among other targets, we found that EWS controls the alternative splicing of the forkhead family transcription factor FOXP1, a pivotal transcriptional regulator of neuronal differentiation, possibly contributing to the switch of gene expression underlying the neuronal differentiation program.

MeSH terms

  • Forkhead Transcription Factors / genetics
  • Forkhead Transcription Factors / metabolism
  • Gene Expression Regulation, Neoplastic
  • Oncogene Proteins, Fusion / genetics
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Proteomics*
  • RNA-Binding Protein EWS / genetics
  • RNA-Binding Protein EWS / metabolism

Substances

  • Forkhead Transcription Factors
  • Oncogene Proteins, Fusion
  • Protein Isoforms
  • RNA-Binding Protein EWS