Distinct roles for canonical and variant histone H3 lysine 36 in Polycomb silencing

Abstract

AbstractPolycomb complexes regulate cell-type specific gene expression programs through heritable silencing of target genes. Trimethylation of histone H3 lysine 27 (H3K27me3) is essential for this process. Perturbation of H3K36 is thought to interfere with H3K27me3. We show that mutants ofDrosophilareplication-dependent(H3.2K36R)or -independent(H3.3K36R)histone H3 genes generally maintain Polycomb silencing and reach later stages of development. In contrast, combined(H3.3K36RH3.2K36R)mutants display widespread Hox gene misexpression and fail to develop past the first larval stage. Chromatin profiling revealed that theH3.2K36Rmutation disrupts H3K27me3 levels broadly throughout silenced domains, whereas these regions are mostly unaffected inH3.3K36Ranimals. Analysis of H3.3 distributions showed that this histone is enriched at presumptive PREs (Polycomb Response Elements) located outside of silenced domains but relatively depleted from those inside. We conclude that H3.2 and H3.3 K36 residues collaborate to repress Hox genes using different mechanisms.Short summaryHistone H3.2 and H3.3 K36 residues ensure Hox gene silencing and enable development by different, but synergistic mechanisms.