p300/CBP-catalyzed acetylation safeguards minor zygotic genome activation via activating DUX

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Abstract

Zygotic genome activation (ZGA), the first transcriptional event at the onset of life, is crucial for early embryonic development. However, the mechanisms that initiate and regulate ZGA in mammals remain poorly understood. In this study, we demonstrate that p300/CBP-catalyzed acetylation plays a vital role in regulating ZGA. Inhibition of p300/CBP acetyltransferase activity results in impaired minor ZGA and a subsequent 2-cell arrest. By profiling the dynamic landscape of p300 during the ZGA stage, we elucidate the distinct patterns of p300 establishment in promoter and enhancer regions. Moreover, p300 recruits RNA polymerase (Pol II) to pre-configure in the promoter regions of ZGA genes, and orchestrates the gradual establishment of enhancer activity during the early 2-cell stage to activate ZGA. Furthermore, p300 enhances minor ZGA by promoting the expression of DUX. Restoring DUX levels, which are diminished due to p300/CBP inhibition, rescues ZGA and embryonic development by re-establishing Pol II enrichment on minor ZGA genes. Overall, our findings elucidate the mechanism by which p300/CBP regulates ZGA through acetylation and activation of the key transcription factor DUX.

Highlights

  • p300/CBP plays a stage-specific role during preimplantation development phase.

  • p300 displays distinctive dynamic changes in promoter and enhancer regions during ZGA stage.

  • p300/CBP-catalyzed acetylation facilitates the pre-configuration and elongation of Pol II at ZGA gene regions.

  • DUX recruits p300 and Pol II to activate minor ZGA genes independently of p300’s catalytic activity.

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