1. A unique bipartite Polycomb signature regulates stimulus-response transcription during development.
- Author
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Kitazawa T, Machlab D, Joshi O, Maiorano N, Kohler H, Ducret S, Kessler S, Gezelius H, Soneson C, Papasaikas P, López-Bendito G, Stadler MB, and Rijli FM
- Subjects
- Animals, Chromatin metabolism, Embryonic Stem Cells physiology, Enhancer of Zeste Homolog 2 Protein genetics, Enhancer of Zeste Homolog 2 Protein metabolism, Epigenesis, Genetic, Histones metabolism, Mice, Transgenic, Mutation, Polycomb-Group Proteins metabolism, Promoter Regions, Genetic, RNA Polymerase II genetics, RNA, Messenger genetics, RNA, Messenger metabolism, Rhombencephalon drug effects, Rhombencephalon embryology, Sensory Receptor Cells physiology, Chromatin genetics, Gene Expression Regulation, Developmental, Genes, Immediate-Early, Polycomb-Group Proteins genetics
- Abstract
Rapid cellular responses to environmental stimuli are fundamental for development and maturation. Immediate early genes can be transcriptionally induced within minutes in response to a variety of signals. How their induction levels are regulated and their untimely activation by spurious signals prevented during development is poorly understood. We found that in developing sensory neurons, before perinatal sensory-activity-dependent induction, immediate early genes are embedded into a unique bipartite Polycomb chromatin signature, carrying active H3K27ac on promoters but repressive Ezh2-dependent H3K27me3 on gene bodies. This bipartite signature is widely present in developing cell types, including embryonic stem cells. Polycomb marking of gene bodies inhibits mRNA elongation, dampening productive transcription, while still allowing for fast stimulus-dependent mark removal and bipartite gene induction. We reveal a developmental epigenetic mechanism regulating the rapidity and amplitude of the transcriptional response to relevant stimuli, while preventing inappropriate activation of stimulus-response genes.
- Published
- 2021
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