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Naked Mole Rat Cells Have a Stable Epigenome that Resists iPSCÂ Reprogramming.
- Source :
-
Stem cell reports [Stem Cell Reports] 2017 Nov 14; Vol. 9 (5), pp. 1721-1734. Date of Electronic Publication: 2017 Oct 26. - Publication Year :
- 2017
-
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.<br /> (Copyright © 2017 The Authors. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Antigens, Polyomavirus Transforming genetics
Antigens, Polyomavirus Transforming metabolism
Chimera embryology
Chromatin genetics
Chromatin metabolism
Fibroblasts cytology
Fibroblasts metabolism
Genome
Induced Pluripotent Stem Cells cytology
Mice
Mole Rats
Animals, Genetically Modified genetics
Cellular Reprogramming
Chimera genetics
Epigenesis, Genetic
Histone Code
Induced Pluripotent Stem Cells metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2213-6711
- Volume :
- 9
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Stem cell reports
- Publication Type :
- Academic Journal
- Accession number :
- 29107597
- Full Text :
- https://doi.org/10.1016/j.stemcr.2017.10.001