Interchromosomal contacts between regulatory regions trigger stable transgenerational epigenetic inheritance in Drosophila

Mol Cell. 2025 Feb 20;85(4):677-691.e6. doi: 10.1016/j.molcel.2024.11.021. Epub 2024 Dec 11.

Abstract

Non-genetic information can be inherited across generations in a process known as transgenerational epigenetic inheritance (TEI). In Drosophila, hemizygosity of the Fab-7 regulatory element triggers inheritance of the histone mark H3K27me3 at a homologous locus on another chromosome, resulting in heritable epigenetic differences in eye color. Here, by mutating transcription factor binding sites within the Fab-7 element, we demonstrate the importance of the proteins pleiohomeotic and GAGA factor in the establishment and maintenance of TEI. We show that these proteins function by recruiting the polycomb repressive complex 2 and by mediating interchromosomal chromatin contacts between Fab-7 and its homologous locus, respectively. Using an in vivo synthetic biology system to induce them, we then show that chromatin contacts alone can establish TEI, providing a mechanism by which hemizygosity of one locus can establish epigenetic memory at another distant locus in trans through chromatin contacts.

Keywords: 3D genome organization; Fab-7; GAGA factor; chromatin contacts; epimutation; polycomb; transgenerational epigenetic inheritance.

MeSH terms

  • Animals
  • Binding Sites
  • Chromatin / genetics
  • Chromatin / metabolism
  • Chromosomes, Insect* / genetics
  • Chromosomes, Insect* / metabolism
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Drosophila Proteins* / genetics
  • Drosophila Proteins* / metabolism
  • Drosophila melanogaster* / genetics
  • Drosophila melanogaster* / metabolism
  • Epigenesis, Genetic*
  • Eye Color / genetics
  • Female
  • Histones / genetics
  • Histones / metabolism
  • Inheritance Patterns*
  • Male
  • Polycomb Repressive Complex 2 / genetics
  • Polycomb Repressive Complex 2 / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • Drosophila Proteins
  • Chromatin
  • Transcription Factors
  • Histones
  • Polycomb Repressive Complex 2
  • DNA-Binding Proteins