Opposing, spatially-determined epigenetic forces impose restrictions on stochastic olfactory receptor choice

Elife. 2023 Dec 18:12:RP87445. doi: 10.7554/eLife.87445.

Abstract

Olfactory receptor (OR) choice represents an example of genetically hardwired stochasticity, where every olfactory neuron expresses one out of ~2000 OR alleles in the mouse genome in a probabilistic, yet stereotypic fashion. Here, we propose that topographic restrictions in OR expression are established in neuronal progenitors by two opposing forces: polygenic transcription and genomic silencing, both of which are influenced by dorsoventral gradients of transcription factors NFIA, B, and X. Polygenic transcription of OR genes may define spatially constrained OR repertoires, among which one OR allele is selected for singular expression later in development. Heterochromatin assembly and genomic compartmentalization of OR alleles also vary across the axes of the olfactory epithelium and may preferentially eliminate ectopically expressed ORs with more dorsal expression destinations from this 'privileged' repertoire. Our experiments identify early transcription as a potential 'epigenetic' contributor to future developmental patterning and reveal how two spatially responsive probabilistic processes may act in concert to establish deterministic, precise, and reproducible territories of stochastic gene expression.

Keywords: chromatin; developmental biology; genomics; heterochromatin; mouse; nuclear architecture; olfaction; patterning.

MeSH terms

  • Alleles
  • Animals
  • Epigenesis, Genetic
  • Epigenomics
  • Mice
  • Olfactory Receptor Neurons*
  • Receptors, Odorant* / genetics

Substances

  • Receptors, Odorant

Associated data

  • GEO/GSE158730
  • GEO/GSE93570