Chromatin Architecture of the Pitx2 Locus Requires CTCF- and Pitx2-Dependent Asymmetry that Mirrors Embryonic Gut Laterality

Cell Rep. 2015 Oct 13;13(2):337-49. doi: 10.1016/j.celrep.2015.08.075. Epub 2015 Sep 24.

Abstract

Expression of Pitx2 on the left side of the embryo patterns left-right (LR) organs including the dorsal mesentery (DM), whose asymmetric cell behavior directs gut looping. Despite the importance of organ laterality, chromatin-level regulation of Pitx2 remains undefined. Here, we show that genes immediately neighboring Pitx2 in chicken and mouse, including a long noncoding RNA (Pitx2 locus-asymmetric regulated RNA or Playrr), are expressed on the right side and repressed by Pitx2. CRISPR/Cas9 genome editing of Playrr, 3D fluorescent in situ hybridization (FISH), and variations of chromatin conformation capture (3C) demonstrate that mutual antagonism between Pitx2 and Playrr is coordinated by asymmetric chromatin interactions dependent on Pitx2 and CTCF. We demonstrate that transcriptional and morphological asymmetries driving gut looping are mirrored by chromatin architectural asymmetries at the Pitx2 locus. We propose a model whereby Pitx2 auto-regulation directs chromatin topology to coordinate LR transcription of this locus essential for LR organogenesis.

Publication types

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

MeSH terms

  • Animals
  • Base Sequence
  • CCCTC-Binding Factor
  • Chick Embryo
  • Chromatin / chemistry
  • Chromatin / genetics*
  • Gene Expression Regulation, Developmental*
  • Genetic Loci
  • Homeobox Protein PITX2
  • Homeodomain Proteins / genetics*
  • Intestinal Mucosa / metabolism*
  • Intestines / embryology
  • Mice
  • Molecular Sequence Data
  • Morphogenesis
  • RNA, Long Noncoding / genetics*
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism*
  • Transcription Factors / genetics*

Substances

  • CCCTC-Binding Factor
  • Chromatin
  • Ctcf protein, mouse
  • Homeodomain Proteins
  • RNA, Long Noncoding
  • Repressor Proteins
  • Transcription Factors

Associated data

  • GEO/GSE71117