Co-transcriptional Loading of RNA Export Factors Shapes the Human Transcriptome

Mol Cell. 2019 Jul 25;75(2):310-323.e8. doi: 10.1016/j.molcel.2019.04.034. Epub 2019 May 16.

Abstract

During gene expression, RNA export factors are mainly known for driving nucleo-cytoplasmic transport. While early studies suggested that the exon junction complex (EJC) provides a binding platform for them, subsequent work proposed that they are only recruited by the cap binding complex to the 5' end of RNAs, as part of TREX. Using iCLIP, we show that the export receptor Nxf1 and two TREX subunits, Alyref and Chtop, are recruited to the whole mRNA co-transcriptionally via splicing but before 3' end processing. Consequently, Alyref alters splicing decisions and Chtop regulates alternative polyadenylation. Alyref is recruited to the 5' end of RNAs by CBC, and our data reveal subsequent binding to RNAs near EJCs. We demonstrate that eIF4A3 stimulates Alyref deposition not only on spliced RNAs close to EJC sites but also on single-exon transcripts. Our study reveals mechanistic insights into the co-transcriptional recruitment of mRNA export factors and how this shapes the human transcriptome.

Keywords: EJC; TREX; alternative polyadenylation; co-transcriptional splicing; nucleo-cytoplasmic transport.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus / genetics
  • Binding Sites
  • DEAD-box RNA Helicases / chemistry
  • DEAD-box RNA Helicases / genetics*
  • Eukaryotic Initiation Factor-4A / chemistry
  • Eukaryotic Initiation Factor-4A / genetics*
  • Exons / genetics
  • Gene Expression Regulation / genetics
  • Humans
  • Nuclear Proteins / chemistry
  • Nuclear Proteins / genetics*
  • Nucleocytoplasmic Transport Proteins / chemistry
  • Nucleocytoplasmic Transport Proteins / genetics*
  • Polyadenylation
  • RNA Transport / genetics
  • RNA, Messenger / chemistry
  • RNA, Messenger / genetics
  • RNA-Binding Proteins / chemistry
  • RNA-Binding Proteins / genetics*
  • Transcription Factors / chemistry
  • Transcription Factors / genetics*
  • Transcription, Genetic*
  • Transcriptome / genetics

Substances

  • ALYREF protein, human
  • NXF1 protein, human
  • Nuclear Proteins
  • Nucleocytoplasmic Transport Proteins
  • RNA, Messenger
  • RNA-Binding Proteins
  • Transcription Factors
  • Eukaryotic Initiation Factor-4A
  • EIF4A3 protein, human
  • DEAD-box RNA Helicases