Disrupting the three-dimensional regulatory topology of the Pitx1 locus results in overtly normal development

Development. 2018 Apr 9;145(7):dev158550. doi: 10.1242/dev.158550.

Abstract

Developmental gene expression patterns are orchestrated by thousands of distant-acting transcriptional enhancers. However, identifying enhancers essential for the expression of their target genes has proven challenging. Maps of long-range regulatory interactions may provide the means to identify enhancers crucial for developmental gene expression. To investigate this hypothesis, we used circular chromosome conformation capture coupled with interaction maps in the mouse limb to characterize the regulatory topology of Pitx1, which is essential for hindlimb development. We identified a robust hindlimb-specific interaction between Pitx1 and a putative hindlimb-specific enhancer. To interrogate the role of this interaction in Pitx1 regulation, we used genome editing to delete this enhancer in mouse. Although deletion of the enhancer completely disrupts the interaction, Pitx1 expression in the hindlimb is only mildly affected, without any detectable compensatory interactions between the Pitx1 promoter and potentially redundant enhancers. Pitx1 enhancer null mice did not exhibit any of the characteristic morphological defects of the Pitx1-/- mutant. Our results suggest that robust, tissue-specific physical interactions at essential developmental genes have limited predictive value for identifying enhancer mutations with strong loss-of-function phenotypes.

Keywords: Enhancer loss-of-function mutations; Enhancer-promoter interactions; Genomics; Limb development.

Publication types

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

MeSH terms

  • Animals
  • Enhancer Elements, Genetic / genetics
  • Extremities / embryology*
  • Gene Expression Regulation, Developmental / genetics*
  • In Situ Hybridization
  • Mice
  • Mice, Knockout
  • Morphogenesis / genetics*
  • Paired Box Transcription Factors / metabolism*
  • Phenotype
  • Real-Time Polymerase Chain Reaction

Substances

  • Paired Box Transcription Factors
  • homeobox protein PITX1