4.8 Article

Opposing microRNA families regulate self-renewal in mouse embryonic stem cells

Journal

NATURE
Volume 463, Issue 7281, Pages 621-U45

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nature08725

Keywords

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Funding

  1. National Institutes of Health (NIH) [K08 NS48118, R01 NS057221]
  2. California Institute of Regenerative Medicine (CIRM) [RS1-00161, RN2-00906]
  3. American Health Assistance Foundation
  4. Pew Charitable Trust
  5. National Science Foundation (NSF)

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When embryonic stem cells (ESCs) differentiate, they must both silence the ESC self-renewal program and activate new tissue-specific programs. In the absence of DGCR8 (Dgcr8(-/-)), a protein required for microRNA (miRNA) biogenesis, mouse ESCs are unable to silence self-renewal. Here we show that the introduction of let-7 miRNAs-a family of miRNAs highly expressed in somatic cells-can suppress self-renewal in Dgcr8(-/-) but not wild-type ESCs. Introduction of ESC cell cycle regulating (ESCC) miRNAs into the Dgcr8(-/-) ESCs blocks the capacity of let-7 to suppress self-renewal. Profiling and bioinformatic analyses show that let-7 inhibits whereas ESCC miRNAs indirectly activate numerous self-renewal genes. Furthermore, inhibition of the let-7 family promotes de-differentiation of somatic cells to induced pluripotent stem cells. Together, these findings show how the ESCC and let-7 miRNAs act through common pathways to alternatively stabilize the self-renewing versus differentiated cell fates.

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