Chromatin Regulation and DNA Repair

A key discovery from the lab is that histone H3K4 methylation marks recruit DNA repair proteins in plants, providing a mechanistic explanation for why mutation rates are lower in gene-rich, H3K4me-enriched regions of the genome. This work has broad implications for understanding the evolution of genome stability.

Current projects:

  • H3K4me-associated hypomutation in plants (with Satoyo Oya)
  • Convergent evolution of epigenome-recruited DNA repair across the Tree of Life
  • Chromatin features predicting intron architecture and mutation rates

Notable papers:

Grey Monroe
Grey Monroe
Associate Professor

Plant genome biologist studying mutation rate variation, epigenome-recruited DNA repair, and functional genomics.