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Stem Cell Reports ; 7(3): 307-315, 2016 09 13.
Article in English | MEDLINE | ID: mdl-27546532

ABSTRACT

Identification of cell-fate determinants for directing stem cell differentiation remains a challenge. Moreover, little is known about how cell-fate determinants are regulated in functionally important subnetworks in large gene-regulatory networks (i.e., GRN motifs). Here we propose a model of stem cell differentiation in which cell-fate determinants work synergistically to determine different cellular identities, and reside in a class of GRN motifs known as feedback loops. Based on this model, we develop a computational method that can systematically predict cell-fate determinants and their GRN motifs. The method was able to recapitulate experimentally validated cell-fate determinants, and validation of two predicted cell-fate determinants confirmed that overexpression of ESR1 and RUNX2 in mouse neural stem cells induces neuronal and astrocyte differentiation, respectively. Thus, the presented GRN-based model of stem cell differentiation and computational method can guide differentiation experiments in stem cell research and regenerative medicine.


Subject(s)
Cell Differentiation/genetics , Cell Lineage/genetics , Gene Expression Regulation, Developmental , Gene Regulatory Networks , Models, Biological , Stem Cells/cytology , Stem Cells/metabolism , Algorithms , Animals , Astrocytes/cytology , Astrocytes/metabolism , Computational Biology/methods , Computer Simulation , Core Binding Factor Alpha 1 Subunit/metabolism , Databases, Genetic , Embryonic Stem Cells/cytology , Embryonic Stem Cells/metabolism , Estrogen Receptor alpha/metabolism , Mice , Neurons/cytology , Neurons/metabolism
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