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dc.contributor.authorCacchiarelli, Davide
dc.contributor.authorTrapnell, Cole
dc.contributor.authorZiller, Michael J.
dc.contributor.authorSoumillon, Magali
dc.contributor.authorCesana, Marcella
dc.contributor.authorKarnik, Rahul
dc.contributor.authorDonaghey, Julie
dc.contributor.authorSmith, Zachary D.
dc.contributor.authorRatanasirintrawoot, Sutheera
dc.contributor.authorZhang, Xiaolan
dc.contributor.authorHo Sui, Shannan J.
dc.contributor.authorWu, Zhaoting
dc.contributor.authorAkopian, Veronika
dc.contributor.authorGifford, Casey A.
dc.contributor.authorDoench, John
dc.contributor.authorRinn, John L.
dc.contributor.authorDaley, George Q.
dc.contributor.authorMeissner, Alexander
dc.contributor.authorMikkelsen, Tarjei S.
dc.contributor.authorLander, Eric Steven
dc.date.accessioned2017-01-18T16:46:55Z
dc.date.available2017-01-18T16:46:55Z
dc.date.issued2015-07
dc.date.submitted2015-03
dc.identifier.issn0092-8674
dc.identifier.issn1097-4172
dc.identifier.urihttp://hdl.handle.net/1721.1/106526
dc.description.abstractInduced 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.en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.cell.2015.06.016en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleIntegrative Analyses of Human Reprogramming Reveal Dynamic Nature of Induced Pluripotencyen_US
dc.typeArticleen_US
dc.identifier.citationCacchiarelli, Davide et al. “Integrative Analyses of Human Reprogramming Reveal Dynamic Nature of Induced Pluripotency.” Cell 162.2 (2015): 412–424.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.mitauthorLander, Eric Steven
dc.relation.journalCellen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsCacchiarelli, Davide; Trapnell, Cole; Ziller, Michael J.; Soumillon, Magali; Cesana, Marcella; Karnik, Rahul; Donaghey, Julie; Smith, Zachary D.; Ratanasirintrawoot, Sutheera; Zhang, Xiaolan; Ho Sui, Shannan J.; Wu, Zhaoting; Akopian, Veronika; Gifford, Casey A.; Doench, John; Rinn, John L.; Daley, George Q.; Meissner, Alexander; Lander, Eric S.; Mikkelsen, Tarjei S.en_US
dspace.embargo.termsNen_US
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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