Variant Histone H2afv reprograms DNA methylation during early zebrafish development

ABSTRACT

The DNA methylome is re-patterned during discrete phases of vertebrate development. In zebrafish, there are 2 waves of global DNA demethylation and re-methylation: the first occurs before gastrulation when the parental methylome is changed to the zygotic pattern and the second occurs after formation of the embryonic body axis, during organ specification. The occupancy of the histone variant H2A.Z and regions of DNA methylation are generally anti-correlated, and it has been proposed that H2A.Z restricts the boundaries of highly methylated regions. While many studies have described the dynamics of methylome changes during early zebrafish development, the factors involved in establishing the DNA methylation landscape in zebrafish embryos have not been identified. We test the hypothesis that the zebrafish ortholog of H2A.Z (H2afv) restricts DNA methylation during development. We find that, in control embryos, bulk genome methylation decreases after gastrulation, with a nadir at the bud stage, and peaks during mid-somitogenesis; by 24 hours post -fertilization, total DNA methylation levels return to those detected in gastrula. Early zebrafish embryos depleted of H2afv have significantly more bulk DNA methylation during somitogenesis, suggesting that H2afv limits methylation during this stage of development. H2afv deficient embryos are small, with multisystemic abnormalities. Genetic interaction experiments demonstrate that these phenotypes are suppressed by depletion of DNA methyltransferase 1 (Dnmt1). This work demonstrates that H2afv is essential for global DNA methylation reprogramming during early vertebrate development and that embryonic development requires crosstalk between H2afv and Dnmt1.

Disclosure of potential conflicts of interest

The authors have no conflicts of interest.

Acknowledgments

The authors wish to acknowledge Brandon Kent for his technical assistance. The work was funded by grants awarded by the UK Medical Research Council (MK/K001949/1 to D.A.M) and NIH (R01DK80789 to K.C.S and UO1AA018663 to D.A.M and J.M). We thank John Parant for providing the constructs encoding H2afva-GFP.

Additional information

Funding

The work was funded by grants awarded by the UK Medical Research Council (MK/K001949/1 to D.A.M) and NIH (R01DK80789 to K.C.S and UO1AA018663 to D.A.M and J.M). We thank John Parant for providing the constructs encoding H2afva-GFP.