Deterministic Restriction on Pluripotent State Dissolution by Cell-Cycle Pathways

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Deterministic Restriction on Pluripotent State Dissolution by Cell-Cycle Pathways
Title:
Deterministic Restriction on Pluripotent State Dissolution by Cell-Cycle Pathways
Journal Title:
Cell
Keywords:
Publication Date:
30 July 2015
Citation:
Kevin Andrew Uy Gonzales, Hongqing Liang, Yee-Siang Lim, Yun-Shen Chan, Jia-Chi Yeo, Cheng-Peow Tan, Bin Gao, Beilin Le, Zi-Ying Tan, Kok-Yao Low, Yih-Cherng Liou, Frederic Bard, Huck-Hui Ng, Deterministic Restriction on Pluripotent State Dissolution by Cell-Cycle Pathways, Cell, Volume 162, Issue 3, 30 July 2015, Pages 564-579, ISSN 0092-8674, http://dx.doi.org/10.1016/j.cell.2015.07.001.
Abstract:
During differentiation, human embryonic stem cells (hESCs) shut down the regulatory network conferring pluripotency in a process we designated pluripotent state dissolution (PSD). In a high-throughput RNAi screen using an inclusive set of differentiation conditions, we identify centrally important and context-dependent processes regulating PSD in hESCs, including histone acetylation, chromatin remodeling, RNA splicing, and signaling pathways. Strikingly, we detected a strong and specific enrichment of cell-cycle genes involved in DNA replication and G2 phase progression. Genetic and chemical perturbation studies demonstrate that the S and G2 phases attenuate PSD because they possess an intrinsic propensity toward the pluripotent state that is independent of G1 phase. Our data therefore functionally establish that pluripotency control is hardwired to the cell-cycle machinery, where S and G2 phase-specific pathways deterministically restrict PSD, whereas the absence of such pathways in G1 phase potentially permits the initiation of differentiation.
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ISSN:
0092-8674
1097-4172
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