| Literature DB >> 26186193 |
Davide Cacchiarelli1, Cole Trapnell2, Michael J Ziller1, Magali Soumillon1, Marcella Cesana3, Rahul Karnik1, Julie Donaghey1, Zachary D Smith1, Sutheera Ratanasirintrawoot3, Xiaolan Zhang4, Shannan J Ho Sui5, Zhaoting Wu3, Veronika Akopian1, Casey A Gifford1, John Doench4, John L Rinn1, George Q Daley3, Alexander Meissner1, Eric S Lander4, Tarjei S Mikkelsen6.
Abstract
Induced pluripotency is a promising avenue for disease modeling and therapy, but the molecular principles underlying this process, particularly in human cells, remain poorly understood due to donor-to-donor variability and intercellular heterogeneity. Here, we constructed and characterized a clonal, inducible human reprogramming system that provides a reliable source of cells at any stage of the process. This system enabled integrative transcriptional and epigenomic analysis across the human reprogramming timeline at high resolution. We observed distinct waves of gene network activation, including the ordered re-activation of broad developmental regulators followed by early embryonic patterning genes and culminating in the emergence of a signature reminiscent of pre-implantation stages. Moreover, complementary functional analyses allowed us to identify and validate novel regulators of the reprogramming process. Altogether, this study sheds light on the molecular underpinnings of induced pluripotency in human cells and provides a robust cell platform for further studies. PAPERCLIP.Entities:
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Year: 2015 PMID: 26186193 PMCID: PMC4511597 DOI: 10.1016/j.cell.2015.06.016
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582