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Differential acetylation of histone H4 lysine during development of in vitro fertilized, cloned and parthenogenetically activated bovine embryos

Maalouf, Walid E.; Alberio, Ramiro; Campbell, Keith H.S.

Authors

Walid E. Maalouf

Profile image of RAMIRO ALBERIO

RAMIRO ALBERIO ramiro.alberio@nottingham.ac.uk
Professor of Developmental Biology

Keith H.S. Campbell



Abstract

The oocyte is remarkable in its ability to remodel parental genomes following fertilization and to reprogram somatic nuclei after nuclear transfer (NT). To characterize the patterns of histone H4 acetylation and DNA methylation during development of bovine gametogenesis and embryogenesis, specific antibodies for histone H4 acetylated at lysine 5 (K5), K8, K12 and K16 residues and for methylated cytosine of CpG dinucleotides were used. Oocytes and sperm lacked the staining for histone acetylation, when DNA methylation staining was intense. In IVF zygotes, both pronuclei were transiently hyper-acetylated. However, the male pronucleus was faster in acquiring acethylated histones, and concurrently it was rapidly demethylated. Both pronuclei were equally acetylated during the S to G2-phase transition, while methylation staining was only still observed in the female pronucleus. In parthenogenetically activated oocytes, acetylation of the female pronucleus was enriched faster, while DNA remained methylated. A transient de-acetylation was observed in NT embryos reconstructed using a non-activated ooplast of a metaphase second arrested oocyte. Remarkably, the intensity of acetylation staining of most H4 lysine residues peaked at the 8-cell stage in IVF embryos, which coincided with zygotic genome activation and with lowest DNA methylation staining. At the blastocyst stage, trophectodermal cells of IVF and parthenogenetic embryos generally demonstrated more intense staining for most acetylated H4 lysine, whilst ICM cells stained very weakly. In contrast methylation of the DNA stained more intensely in ICM. NT blastocysts showed differential acetylation of blastomeres but not methylation. The inverse association of histone lysine acetylation and DNA methylation at different vital embryo stages suggests a mechanistically significant relationship. The complexities of these epigenetic interactions are discussed. © 2008 Landes Bioscience.

Citation

Maalouf, W. E., Alberio, R., & Campbell, K. H. (2008). Differential acetylation of histone H4 lysine during development of in vitro fertilized, cloned and parthenogenetically activated bovine embryos. Epigenetics, 3(4), 199-209. https://doi.org/10.4161/epi.3.4.6497

Journal Article Type Article
Acceptance Date Jun 24, 2008
Online Publication Date Jul 31, 2008
Publication Date Jan 1, 2008
Deposit Date Jan 6, 2020
Journal Epigenetics
Print ISSN 1559-2294
Electronic ISSN 1559-2308
Publisher Taylor and Francis
Peer Reviewed Peer Reviewed
Volume 3
Issue 4
Pages 199-209
DOI https://doi.org/10.4161/epi.3.4.6497
Public URL https://nottingham-repository.worktribe.com/output/3186175
Publisher URL https://www.tandfonline.com/doi/abs/10.4161/epi.3.4.6497