| Literature DB >> 33440162 |
Victor Olariu1, Mary A Yui2, Pawel Krupinski1, Wen Zhou2, Julia Deichmann1, Emil Andersson1, Ellen V Rothenberg3, Carsten Peterson4.
Abstract
Intrathymic development of committed progenitor (pro)-T cells from multipotent hematopoietic precursors offers an opportunity to dissect the molecular circuitry establishing cell identity in response to environmental signals. This transition encompasses programmed shutoff of stem/progenitor genes, upregulation of T cell specification genes, proliferation, and ultimately commitment. To explain these features in light of reported cis-acting chromatin effects and experimental kinetic data, we develop a three-level dynamic model of commitment based upon regulation of the commitment-linked gene Bcl11b. The levels are (1) a core gene regulatory network (GRN) architecture from transcription factor (TF) perturbation data, (2) a stochastically controlled chromatin-state gate, and (3) a single-cell proliferation model validated by experimental clonal growth and commitment kinetic assays. Using RNA fluorescence in situ hybridization (FISH) measurements of genes encoding key TFs and measured bulk population dynamics, this single-cell model predicts state-switching kinetics validated by measured clonal proliferation and commitment times. The resulting multi-scale model provides a mechanistic framework for dissecting commitment dynamics.Entities:
Keywords: T cell development; epigenetic modeling; experimental validations; kinetic measurements; population modeling; proliferation measurements; single-cell measurements; stochastic simulations; transcriptional modeling
Mesh:
Year: 2021 PMID: 33440162 PMCID: PMC7943435 DOI: 10.1016/j.celrep.2020.108622
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423