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Naked Mole Rat Cells Have a Stable Epigenome that Resists iPSC Reprogramming
Li Tan1, Zhonghe Ke2, Gregory Tombline2
1Department of Biology, University of Rochester, Rochester, NY 14627, USA; Laboratory of Epigenetics, Institutes of Biomedical Sciences and Department of Cellular and Genetic Medicine, School of Basic Medical Sciences, Shanghai Medical College of Fudan University, Shanghai 200032, P. R. China.
Abstract:
Naked mole rat (NMR) is a valuable model for aging and cancer research due to its exceptional longevity and cancer resistance. We observed that the reprogramming efficiency of NMR fibroblasts in response to OSKM was drastically lower than that of mouse fibroblasts. Expression of SV40 LargeT antigen (LT) dramatically improved reprogramming of NMR fibroblasts. Inactivation of Rb alone, but not p53, was sufficient to improve reprogramming efficiency, suggesting that NMR chromatin may be refractory to reprogramming. Analysis of the global histone landscape revealed that NMR had higher levels of repressive H3K27 methylation marks and lower levels of activating H3K27 acetylation marks than mouse. ATAC-seq revealed that in NMR, promoters of reprogramming genes were more closed than mouse promoters, while expression of LT led to massive opening of the NMR promoters. These results suggest that NMR displays a more stable epigenome that resists de-differentiation, contributing to the cancer resistance and longevity of this species.
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