Reprogramming of somatic cells to induced pluripotent stem cells rewrites the code of cell fate at the chromatin level. Yet, little is known about this process physically. Here, we describe a fluorescence recovery after photobleaching method to assess the dynamics of heterochromatin/euchromatin and show significant heterochromatin loosening at the initial stage of reprogramming. We identify growth arrest and DNA damage‐inducible protein a (Gadd45a) as a chromatin relaxer in mouse embryonic fibroblasts, which also enhances somatic cell reprogramming efficiency. We show that residue glycine 39 (G39) in Gadd45a is essential for interacting with core histones, opening chromatin and enhancing reprogramming. We further demonstrate that Gadd45a destabilizes histone–DNA interactions and facilitates the binding of Yamanaka factors to their targets for activation. Our study provides a method to screen factors that impact on chromatin structure in live cells, and identifies Gadd45a as a chromatin relaxer.
Using a histone FRAP method, this study identifies Gadd45a as a chromatin relaxer and somatic cell reprogramming enhancer. Gadd45a destabilizes histone–DNA interactions and facilitates the binding of Yamanaka factors to their targets.
FRAP is used to assess heterochromatin/euchromatin dynamics in somatic cell reprogramming.
Gadd45a is a chromatin relaxer and improves somatic cell reprogramming.
Gadd45a destabilizes histone–DNA interactions and facilitates the binding of Yamanaka factors to their targets.
EMBO Reports (2016) 17: 1641–1656
- Received March 18, 2016.
- Revision received August 27, 2016.
- Accepted September 2, 2016.
- © 2016 The Authors
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