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  • Emerging roles of the histo...
    Cheloufi, Sihem; Hochedlinger, Konrad

    Current opinion in genetics & development, 10/2017, Letnik: 46
    Journal Article

    •Recent RNAi screens have identified CAF-1 as a barrier to cell fate change in various cellular and developmental systems.•Effects of CAF-1 suppression are cell context-dependent, facilitating either differentiation, dedifferentiation or lineage conversion.•CAF-1 suppression influences cellular plasticity by altering local or global chromatin states. During embryonic development, cells become progressively restricted in their differentiation potential. This is thought to be regulated by dynamic changes in chromatin structure and associated modifications, which act together to stabilize distinct specialized cell lineages. Remarkably, differentiated cells can be experimentally reprogrammed to a stem cell-like state or to alternative lineages. Thus, cellular reprogramming provides a valuable platform to study the mechanisms that normally safeguard cell identity and uncover factors whose manipulation facilitates cell fate transitions. Recent work has identified the chromatin assembly factor complex CAF-1 as a potent barrier to cellular reprogramming. In addition, CAF-1 has been implicated in the reversion of pluripotent cells to a totipotent-like state and in various lineage conversion paradigms, suggesting that modulation of CAF-1 levels may endow cells with a developmentally more plastic state. Here, we review these exciting results, discuss potential mechanisms and speculate on the possibility of exploiting chromatin assembly pathways to manipulate cell identity.