Spatial epigenetic control of mono- and bistable gene expression.
Ontology highlight
ABSTRACT: Bistability in signaling networks is frequently employed to promote stochastic switch-like transitions between cellular differentiation states. Differentiation can also be triggered by antagonism of activators and repressors mediated by epigenetic processes that constitute regulatory circuits anchored to the chromosome. Their regulatory logic has remained unclear. A reaction-diffusion model reveals that the same reaction mechanism can support both graded monostable and switch-like bistable gene expression, depending on whether recruited repressor proteins generate a single silencing gradient or two interacting gradients that flank a gene. Our experiments confirm that chromosomal recruitment of activator and repressor proteins permits a plastic form of control; the stability of gene express
SUBMITTER: Kelemen JZ
PROVIDER: S-EPMC2838748 | biostudies-literature | 2010 Mar
REPOSITORIES: biostudies-literature
ACCESS DATA