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dc.contributor.authorChakraborty, Meenakshi
dc.contributor.authorHu, Sofia
dc.contributor.authorVisness, Erica
dc.contributor.authorDel Giudice, Marco
dc.contributor.authorDe Martino, Andrea
dc.contributor.authorBosia, Carla
dc.contributor.authorSharp, Phillip A
dc.contributor.authorGarg, Salil
dc.date.accessioned2021-10-27T20:34:27Z
dc.date.available2021-10-27T20:34:27Z
dc.date.issued2020
dc.identifier.urihttps://hdl.handle.net/1721.1/136242
dc.description.abstract© 2020 National Academy of Sciences. All rights reserved. Pluripotent embryonic stem cells (ESCs) contain the potential to form a diverse array of cells with distinct gene expression states, namely the cells of the adult vertebrate. Classically, diversity has been attributed to cells sensing their position with respect to external morphogen gradients. However, an alternative is that diversity arises in part from cooption of fluctuations in the gene regulatory network. Here we find ESCs exhibit intrinsic heterogeneity in the absence of external gradients by forming interconverting cell states. States vary in developmental gene expression programs and display distinct activity of microRNAs (miRNAs). Notably, miRNAs act on neighborhoods of pluripotency genes to increase variation of target genes and cell states. Loss of miRNAs that vary across states reduces target variation and delays state transitions, suggesting variable miRNAs organize and propagate variation to promote state transitions. Together these findings provide insight into how a gene regulatory network can coopt variation intrinsic to cell systems to form robust gene expression states. Interactions between intrinsic heterogeneity and environmental signals may help achieve developmental outcomes.
dc.language.isoen
dc.publisherProceedings of the National Academy of Sciences
dc.relation.isversionof10.1073/PNAS.1920695117
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
dc.sourcePNAS
dc.titleMicroRNAs organize intrinsic variation into stem cell states
dc.typeArticle
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MIT
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biology
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technology
dc.relation.journalProceedings of the National Academy of Sciences of the United States of America
dc.eprint.versionFinal published version
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2021-08-02T17:55:56Z
dspace.orderedauthorsChakraborty, M; Hu, S; Visness, E; Del Giudice, M; De Martino, A; Bosia, C; Sharp, PA; Garg, S
dspace.date.submission2021-08-02T17:55:58Z
mit.journal.volume117
mit.journal.issue12
mit.licensePUBLISHER_POLICY
mit.metadata.statusAuthority Work and Publication Information Needed


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