Chromatin condensation fluctuations rather than steady-state predict chromatin accessibility

Audugé N., Padilla-Parra S., Tramier M., Borghi N., Coppey-Moisan M.

<jats:title>Abstract</jats:title> <jats:p>Chromatin accessibility to protein factors is critical for genome activities. However, the dynamic properties of chromatin higher-order structures that regulate its accessibility are poorly understood. Here, we took advantage of the microenvironment sensitivity of the fluorescence lifetime of EGFP-H4 histone incorporated in chromatin to map in the nucleus of live cells the dynamics of chromatin condensation and its direct interaction with a tail acetylation recognition domain (the double bromodomain module of human TAFII250, dBD). We reveal chromatin condensation fluctuations supported by mechanisms fundamentally distinct from that of condensation. Fluctuations are spontaneous, yet their amplitudes are affected by their sub-nuclear localization and by distinct and competing mechanisms dependent on histone acetylation, ATP and both. Moreover, we show that accessibility of acetylated histone H4 to dBD is not restricted by chromatin condensation nor predicted by acetylation, rather, it is predicted by chromatin condensation fluctuations.</jats:p>

DOI

10.1093/nar/gkz373

Type

Journal article

Journal

Nucleic Acids Research

Publisher

Oxford University Press (OUP)

Publication Date

09/07/2019

Volume

47

Pages

6184 - 6194

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