Multiple Arkadia/RNF111 structures coordinate its Polycomb body association and transcriptional control

Mol Cell Biol. 2014 Aug;34(16):2981-95. doi: 10.1128/MCB.00036-14. Epub 2014 Jun 9.

Abstract

The RING domain protein Arkadia/RNF111 is a ubiquitin ligase in the transforming growth factor β (TGFβ) pathway. We previously identified Arkadia as a small ubiquitin-like modifier (SUMO)-binding protein with clustered SUMO-interacting motifs (SIMs) that together form a SUMO-binding domain (SBD). However, precisely how SUMO interaction contributes to the function of Arkadia was not resolved. Through analytical molecular and cell biology, we found that the SIMs share redundant function with Arkadia's M domain, a region distinguishing Arkadia from its paralogs ARKL1/ARKL2 and the prototypical SUMO-targeted ubiquitin ligase (STUbL) RNF4. The SIMs and M domain together promote both Arkadia's colocalization with CBX4/Pc2, a component of Polycomb bodies, and the activation of a TGFβ pathway transcription reporter. Transcriptome profiling through RNA sequencing showed that Arkadia can both promote and inhibit gene expression, indicating that Arkadia's activity in transcriptional control may depend on the epigenetic context, defined by Polycomb repressive complexes and DNA methylation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Animals
  • Base Sequence
  • Carrier Proteins / genetics
  • DNA Methylation
  • Gene Expression Profiling
  • Gene Expression Regulation / genetics*
  • HEK293 Cells
  • Humans
  • Ligases
  • Mice
  • Nuclear Proteins / biosynthesis
  • Nuclear Proteins / genetics*
  • Polycomb-Group Proteins / genetics
  • Promoter Regions, Genetic
  • Protein Structure, Tertiary
  • Schizosaccharomyces / genetics
  • Sequence Analysis, RNA
  • Signal Transduction / genetics
  • Small Ubiquitin-Related Modifier Proteins / genetics*
  • Transcription Factors / genetics
  • Transcription, Genetic
  • Transforming Growth Factor beta / genetics*
  • Transforming Growth Factor beta / metabolism
  • Ubiquitin-Protein Ligases / biosynthesis
  • Ubiquitin-Protein Ligases / genetics*

Substances

  • Adaptor Proteins, Signal Transducing
  • C18ORF25 protein, human
  • Carrier Proteins
  • Nuclear Proteins
  • Polycomb-Group Proteins
  • RNF4 protein, human
  • Small Ubiquitin-Related Modifier Proteins
  • Transcription Factors
  • Transforming Growth Factor beta
  • RNF111 protein, human
  • Ubiquitin-Protein Ligases
  • Ligases
  • CBX4 protein, human