Essential Role of Nr2f Nuclear Receptors in Patterning the Vertebrate Upper Jaw

Dev Cell. 2018 Feb 5;44(3):337-347.e5. doi: 10.1016/j.devcel.2017.12.022. Epub 2018 Jan 18.

Abstract

The jaw is central to the extensive variety of feeding and predatory behaviors across vertebrates. The bones of the lower but not upper jaw form around an early-developing cartilage template. Whereas Endothelin1 patterns the lower jaw, the factors that specify upper-jaw morphology remain elusive. Here, we identify Nuclear Receptor 2f genes (Nr2fs) as enriched in and required for upper-jaw formation in zebrafish. Combinatorial loss of Nr2fs transforms maxillary components of the upper jaw into lower-jaw-like structures. Conversely, nr2f5 misexpression disrupts lower-jaw development. Genome-wide analyses reveal that Nr2fs repress mandibular gene expression and early chondrogenesis in maxillary precursors. Rescue of lower-jaw defects in endothelin1 mutants by reducing Nr2f dosage further demonstrates that Nr2f expression must be suppressed for normal lower-jaw development. We propose that Nr2fs shape the upper jaw by protecting maxillary progenitors from early chondrogenesis, thus preserving cells for later osteogenesis.

Keywords: COUP-TF; Endothelin1; Nr2f1; Nr2f2; Nr2f5; bone; cartilage; jaw; nuclear receptor; pharyngeal arches.

Publication types

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

MeSH terms

  • Animals
  • Body Patterning / physiology*
  • Chondrogenesis / physiology
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Endothelin-1 / genetics
  • Endothelin-1 / metabolism*
  • Gene Expression Regulation, Developmental
  • Jaw / embryology*
  • Jaw / physiology
  • Maxilla / embryology*
  • Maxilla / physiology
  • Mutation
  • Odontogenesis / physiology
  • Signal Transduction
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Zebrafish / embryology*
  • Zebrafish / physiology
  • Zebrafish Proteins / genetics
  • Zebrafish Proteins / metabolism*

Substances

  • DNA-Binding Proteins
  • Endothelin-1
  • Transcription Factors
  • Zebrafish Proteins
  • edn1 protein, zebrafish
  • nr2f1a protein, zebrafish