microRNAs regulate human embryonic stem cell division

Junlin Qi(California Institute for Regenerative Medicine), Jenn‐Yah Yu(National Yang Ming Chiao Tung University), Halyna R. Shcherbata(Max Planck Society), Julie Mathieu(University of Washington), Amy Jia Wang(University of Washington), Sudeshna Seal(University of Washington), Wenyu Zhou(University of Washington), Bradford Stadler(University of Washington), David Bourgin(University of Washington), Linlin Wang(University of Washington), Angel Nelson(University of Washington), Carol B. Ware(University of Washington), Christopher K. Raymond(Merck Biopharma Co., Ltd. (Japan)), Lee P. Lim(Merck Biopharma Co., Ltd. (Japan)), Jill Magnus(Merck Biopharma Co., Ltd. (Japan)), Irena L. Ivanovska(Merck Biopharma Co., Ltd. (Japan)), Robert L. Diaz(Merck Biopharma Co., Ltd. (Japan)), Alexey Ball(Merck Biopharma Co., Ltd. (Japan)), Michele A. Cleary(Mercy University Hospital), Hannele Ruohola‐Baker(University of Washington)
Cell Cycle
November 15, 2009
Cited by 160Open Access
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Abstract

microRNAs (miRNAs) regulate numerous physiological processes such as cell division and differentiation in many tissue types including stem cells. To probe the role that miRNAs play in regulating processes relevant to embryonic stem cell biology, we used RNA interference to silence DICER and DROSHA, the two main miRNA processing enzymes. Consistent with a role for miRNAs in maintaining normal stem cell division and renewal, we found that perturbation of miRNA pathway function in human embryonic stem cells (hESCs) attenuates cell proliferation. Normal cell growth can be partially restored by introduction of the mature miRNAs miR-195 and miR-372. These miRNAs regulate two tumor suppressor genes, respectively: WEE1, which encodes a negative G2/M kinase modulator of the CycB/CDK complex and CDKN1A, which encodes p21, a CycE/CDK cyclin dependent kinase inhibitor that regulates the G1/S transition. We show that in wild-type hESCs, WEE 1 levels control the rate of hESC division, whereas p21 levels must be maintained at a low level for hESC division to proceed. These data support a model for hESC cell cycle control in which miRNAs regulate negative cell cycle modulators at two phases of the cell cycle to ensure proper replenishment of the stem cell population.


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