PLoS Computational Biology · 2014 · 128 citations · 51 references
Life SciencesCell BiologyDevelopmental BiologyEpigeneticsGene ExpressionGene Regulatory NetworksCell Fate ModelingCell-fate DynamicsCellular ReprogrammingEpigenetic Regulation In DevelopmentEpigenetic Regulatory NetworksEpigenetic ReprogrammingAttractor DynamicsAttractor NetworksCell Fate ConversionCell Fate DecisionsEpigenetic Landscape DynamicsEpigenetic Regulation Of Cell IdentityEpigenetic Regulation Of FateEpigenomic Landscape
Development is often depicted as a rugged epigenetic landscape where cell fates are dynamic attractors that can shift in response to external signals. The study introduces a framework that constructs epigenetic landscapes by integrating genomic data with spin‑glass physics techniques. The framework combines genomic data with spin‑glass physics and is validated by reanalyzing existing datasets. The model predicts partially reprogrammed cells are hybrids co‑expressing genes from multiple fates, reproduces known reprogramming protocols, and identifies candidate transcription factors for novel fates, underscoring epigenetic landscapes as a powerful paradigm.
A common metaphor for describing development is a rugged "epigenetic landscape" where cell fates are represented as attracting valleys resulting from a complex regulatory network. Here, we introduce a framework for explicitly constructing epigenetic landscapes that combines genomic data with techniques from spin-glass physics. Each cell fate is a dynamic attractor, yet cells can change fate in response to external signals. Our model suggests that partially reprogrammed cells are a natural consequence of high-dimensional landscapes, and predicts that partially reprogrammed cells should be hybrids that co-express genes from multiple cell fates. We verify this prediction by reanalyzing existing datasets. Our model reproduces known reprogramming protocols and identifies candidate transcription factors for reprogramming to novel cell fates, suggesting epigenetic landscapes are a powerful paradigm for understanding cellular identity.
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Construction of a genetic toggle switch in Escherichia coli
Timothy S. Gardner, Charles R. Cantor, James J. Collins · Nature · 2000 · 4.4K citations