1. Jmjd3 inhibits reprogramming by upregulating expression of INK4a/Arf and targeting PHF20 for ubiquitination.
- Author
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Zhao W, Li Q, Ayers S, Gu Y, Shi Z, Zhu Q, Chen Y, Wang HY, and Wang RF
- Subjects
- Animals, Cyclin-Dependent Kinase Inhibitor p16 genetics, DNA-Binding Proteins, Embryo, Mammalian cytology, Fibroblasts metabolism, Kinetics, Mice, Proteasome Endopeptidase Complex metabolism, Proteolysis, Transcription Factors, Tripartite Motif Proteins, Ubiquitin-Protein Ligases metabolism, Ubiquitination, Up-Regulation, Cellular Reprogramming, Homeodomain Proteins metabolism, Induced Pluripotent Stem Cells metabolism, Jumonji Domain-Containing Histone Demethylases metabolism
- Abstract
Although somatic cell reprogramming to generate inducible pluripotent stem cells (iPSCs) is associated with profound epigenetic changes, the roles and mechanisms of epigenetic factors in this process remain poorly understood. Here, we identify Jmjd3 as a potent negative regulator of reprogramming. Jmjd3-deficient MEFs produced significantly more iPSC colonies than did wild-type cells, whereas ectopic expression of Jmjd3 markedly inhibited reprogramming. We show that the inhibitory effects of Jmjd3 are produced through both histone demethylase-dependent and -independent pathways. The latter pathway involves Jmjd3 targeting of PHF20 for ubiquitination and degradation via recruitment of an E3 ligase, Trim26. Importantly, PHF20-deficient MEFs could not be converted to fully reprogrammed iPSCs, even with knockdown of Jmjd3, Ink4a, or p21, indicating that PHF20 is required for reprogramming. Our findings demonstrate, to the best of our knowledge, a previously unrecognized role of Jmjd3 in cellular reprogramming and provide molecular insight into the mechanisms by which the Jmjd3-PHF20 axis controls this process., (Copyright © 2013 Elsevier Inc. All rights reserved.)
- Published
- 2013
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