Stem Cell Proliferation Is Kept in Check by the Chromatin Regulators Kismet/CHD7/CHD8 and Trr/MLL3/4

Chromatin remodeling accompanies differentiation, however, its role in self-renewal is less well understood. We report that in Drosophila, the chromatin remodeler Kismet/CHD7/CHD8 limits intestinal stem cell (ISC) number and proliferation without affecting differentiation. Stem-cell-specific whole-genome profiling of Kismet revealed its enrichment at transcriptionally active regions bound by RNA polymerase II and Brahma, its recruitment to the transcription start site of activated genes and developmental enhancers and its depletion from regions bound by Polycomb, Histone H1, and heterochromatin Protein 1. We demonstrate that the Trithorax-related/MLL3/4 chromatin modifier regulates ISC proliferation, colocalizes extensively with Kismet throughout the ISC genome, and co-regulates genes in ISCs, including Cbl, a negative regulator of Epidermal Growth Factor Receptor (EGFR). Loss of kismet or trr leads to elevated levels of EGFR protein and signaling, thereby promoting ISC self-renewal. We propose that Kismet with Trr establishes a chromatin state that limits EGFR proliferative signaling, preventing tumor-like stem cell overgrowths. [Display omitted] •Chromatin modifiers Kismet and Trr limit intestinal stem cell proliferation•Kismet and Trr colocalize at transcriptionally active regions and co-regulate genes•EGFR negative regulator Cbl is a target gene of Kismet and Trr•Kismet and Trr limit EGFR signaling in ISCs, preventing tumor-like ISC accumulation Stem cell proliferation control is essential to maintaining tissue homeostasis. Gervais et al. compare Drosophila intestinal stem cell (ISC) whole-genome profiling of chromatin modifier Kismet/CHD7/CHD8 binding to DamID reporters of different chromatin states and demonstrate that Kismet and Trr/MLL3/4 are regulators of ISC self-renewal by limiting EGFR signaling.