| First Author | Rollo C | Year | 2017 |
| Journal | Reproduction | Volume | 154 |
| Issue | 4 | Pages | 375-385 |
| PubMed ID | 28878090 | Mgi Jnum | J:250236 |
| Mgi Id | MGI:5923296 | Doi | 10.1530/REP-17-0112 |
| Citation | Rollo C, et al. (2017) Histone 3 lysine 9 acetylation is a biomarker of the effects of culture on zygotes. Reproduction 154(4):375-385 |
| abstractText | Acetylation of histone proteins is a major determinant of chromatin structure and function. Fertilisation triggers a round of chromatin remodelling that prepares the genome for the first round of transcription from the new embryonic genome. In this study we confirm that fertilisation leads to a marked progressive increase in the level of histone 3 lysine 9 acetylation in both the paternally and maternally derived genomes. The culture of zygotes in simple defined media caused a marked increase in the global level of acetylation and this affected the male pronucleus more than the female. The culture created a marked asymmetry in staining between the two pronuclei that was not readily detected in zygotes collected directly from the reproductive tract and was ameliorated to some extent by optimized culture media. The increased acetylation caused by culture resulted in increased transcription of Hspa1b, a marker of embryonic genome activation. Pharmacological analyses showed the hyperacetylation of H3K9 and the increased expression of Hspa1b caused by culture were due to the altered net activity of a range of histone acetylases and deacetylases. The marked hyperacetylation of histone 3 lysine 9 caused by culture of zygotes may serve as an early biomarker for the effects of culture on the normal function of the embryo. The results also provide further evidence for an effect of the stresses associated with assisted reproductive technologies on the normal patterns of epigenetic reprogramming in the early embryo. |
