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Foshay, K. M.

Publications and source records attributed to Foshay, K. M..

2 recordsLinked to original sources

Mechanistic basis of lineage restriction

Lineage restriction is the biological phenomenon where cells lose developmental potency during differentiation for all except their adopted lineages. Lineage restriction is foundational to multicellularity as it secures the functional identities of the myriad cell types in the body. As yet, the mechanisms of lineage restriction remain enigmatic. By developing Potency-Seq to systematically map transcriptional potency of genes across the genome, we uncovered a link between the restriction of developmental potency of cells and the occlusion of transcriptional potency of their genomes. We further showed that, strikingly, genes can undergo irreversible occlusion of their transcriptional potency simply by chromatinization into the nucleosomal form with unmodified histones. These findings led to a comprehensive mechanistic account of lineage restriction as driven by gene occlusion. Specifically, naive pluripotent stem cells at the onset of development possess the unique capacity to erase occlusion globally to reset full transcriptional potency of the genome, which in turn establishes full developmental potency of the cells. Such deocclusion capacity is abolished when cells progress from naive to primed pluripotency. From this stage onward, lineage-inappropriate genes can undergo nucleosome-mediated occlusion in an irreversible manner when their cognate transcription factors (TFs) and/or placeholder factors (PFs) no longer exist in cells to protect them. Consequently, the transcriptionally potent portion of the genome shrinks progressively and irreversibly during differentiation, thus permanently restricting the developmental potency of differentiating cells. ONE-SENTENCE SUMMARYDevelopmental potency of cells is linked to transcriptional potency of their genomes

developmental biology↗

Capacity to erase gene occlusion is a defining feature distinguishing naive from primed pluripotency

Pluripotent stem cells can exist in either the naive state representing a developmental blank slate or the downstream primed state poised for differentiation. Currently, known differences between these two states are mostly phenomenological, and none can adequately explain why the two states should differ in developmental priming. Gene occlusion is a mode of epigenetic inactivation that renders genes unresponsive to their cognate transcriptional activators. It plays a crucial role in lineage restriction. Here, we report that a defining feature distinguishing the two pluripotent states lies in the ability of naive but not primed cells to erase occlusion. This "deocclusion" capacity requires Esrrb, a gene expressed only in the naive but not primed state. Notably, Esrrb silencing in the primed state is itself due to occlusion. Collectively, our data argue that the Esrrb-dependent deocclusion capacity in naive cells is key for sustaining naive pluripotency, and the loss of this capacity in the primed state via the occlusion of Esrrb poises cells for differentiation.

molecular biology↗