Cold‐induced deposition of bivalent H3K4me3‐H3K27me3 modification and nucleosome depletion in Arabidopsis

Abstract

SUMMARYEpigenetic regulation of gene expression plays a crucial role in plant development and environmental adaptation. The H3K4me3 and H3K27me3 have not only been discovered in the regulation of gene expression in multiple biological processes but also in responses to abiotic stresses in plants. However, evidence for the presence of both H3K4me3 and H3K27me3 on the same nucleosome is sporadic. Cold‐induced deposition of bivalent H3K4me3‐H3K27me3 modifications and nucleosome depletion over a considerable number of active genes is documented in potato tubers and provides clues on an additional role of the bivalent modifications. Limited by the available information of genes encoding PcG/TrxG proteins as well as their corresponding mutants in potatoes, the molecular mechanism underlying the cold‐induced deposition of the bivalent mark remains elusive. In this study, we found a similar deposition of the bivalent H3K4me3‐H3K27me3 mark over 2129 active genes in cold‐treated Arabidopsis Col‐0 seedlings. The expression levels of the bivalent mark‐associated genes tend to be independent of bivalent modification levels. However, these genes were associated with greater chromatin accessibility, presumably to provide a distinct chromatin environment for gene expression. In mutants clf28 and lhp1, failure to deposit H3K27me3 in active genes upon cold treatment implies that the CLF is potentially involved in cold‐induced deposition of H3K27me3, with assistance from LHP1. Failure to deposit H3K4me3 during cold treatment in atx1‐2 suggests a regulatory role of ATX1 in the deposition of H3K4me3. In addition, we observed a cold‐induced global reduction in nucleosome occupancy, which is potentially mediated by LHP1 in an H3K27me3‐dependent manner.