Structural insights into the targeting of mRNA GU-rich elements by the three RRMs of CELF1

Nucleic Acids Res. 2013 Aug;41(14):7153-66. doi: 10.1093/nar/gkt470. Epub 2013 Jun 6.

Abstract

The CUG-BP, Elav-like family (CELF) of RNA-binding proteins control gene expression at a number of different levels by regulating pre-mRNA splicing, deadenylation and mRNA stability. We present structural insights into the binding selectivity of CELF member 1 (CELF1) for GU-rich mRNA target sequences of the general form 5'-UGUNxUGUNyUGU and identify a high affinity interaction (Kd ∼ 100 nM for x = 2 and y = 4) with simultaneous binding of all three RNA recognition motifs within a single 15-nt binding element. RNA substrates spin-labelled at either the 3' or 5' terminus result in differential nuclear magnetic resonance paramagnetic relaxation enhancement effects, which are consistent with a non-sequential 2-1-3 arrangement of the three RNA recognition motifs on UGU sites in a 5' to 3' orientation along the RNA target. We further demonstrate that CELF1 binds to dispersed single-stranded UGU sites at the base of an RNA hairpin providing a structural rationale for recognition of CUG expansion repeats and splice site junctions in the regulation of alternative splicing.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Electron Spin Resonance Spectroscopy
  • Guanine / analysis
  • Models, Molecular
  • Nuclear Magnetic Resonance, Biomolecular
  • Protein Binding
  • Protein Structure, Tertiary
  • RNA, Messenger / chemistry*
  • RNA, Messenger / metabolism
  • RNA-Binding Proteins / chemistry*
  • RNA-Binding Proteins / metabolism
  • Uridine / analysis
  • Xenopus Proteins / chemistry*
  • Xenopus Proteins / metabolism

Substances

  • CELF1 protein, Xenopus
  • RNA, Messenger
  • RNA-Binding Proteins
  • Xenopus Proteins
  • Guanine
  • Uridine