H3K27me3 dictates atypical genome-nuclear lamina interactions and allelic asymmetry during early embryogenesis

Guerreiro, I.; Rang, F. J.; Kawamura, Y. K.; Groenveld, F. C.; van Beek, R. E.; Lochs, S. J. A.; Boele, E.; Peters, A.; Kind, J.

doi:10.1101/2023.02.06.527307

bioRxiv · 10.1101/2023.02.06.527307

H3K27me3 dictates atypical genome-nuclear lamina interactions and allelic asymmetry during early embryogenesis

Guerreiro, I.·Rang, F. J.·Kawamura, Y. K.·Groenveld, F. C.·van Beek, R. E.·Lochs, S. J. A.·Boele, E.·Peters, A.·Kind, J.

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Abstract

The very first days of mammalian embryonic development are accompanied by epigenetic reprogramming and extensive changes in nuclear organization. In particular, genomic regions located at the periphery of the nucleus, termed lamina-associated domains (LADs), undergo major rearrangements after fertilization. However, the role of LADs in regulating gene expression as well as the interplay with various chromatin marks during preimplantation development remains elusive. In this study, we obtained single-cell LAD profiles coupled with the corresponding gene expression readout throughout the first days of mouse development. We detect extensive cell-cell LAD variability at the 2-cell stage, which surprisingly does not seem to functionally affect gene expression. This suggests an unusual uncoupling between 3D-nuclear genome organization and gene expression during totipotent developmental stages. By analyzing LAD dynamics and chromatin states across early developmental stages in an allelic-specific manner, we identify genomic regions that transiently detach from the nuclear lamina and are enriched by non-canonical H3K27me3. Upon maternal knock-out of a component of the Polycomb repressive complex 2 and concomitant loss of H3K27me3 during early embryogenesis, these regions relocate to the lamina at the 2-cell stage. Our results suggest that H3K27me3 is the prime determinant in establishing the atypical distribution of the genome at the nuclear periphery during the first days of embryonic development. This study provides insight into the molecular mechanisms regulating nuclear organization of parental genomes during very early mammalian development.

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Guerreiro, I., Rang, F. J., Kawamura, Y. K., Groenveld, F. C., van Beek, R. E., Lochs, S. J. A., Boele, E., Peters, A., Kind, J.. 2023-02-07. H3K27me3 dictates atypical genome-nuclear lamina interactions and allelic asymmetry during early embryogenesis. https://doi.org/10.1101/2023.02.06.527307

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