Effects of In Vitro Maturation on Histone Acetylation in Metaphase II Oocytes and Early Cleavage Embryos

Author:

Wang Ning1,Le Fang1,Zhan Qi-Tao1,Li Li1,Dong Min-Yue1,Ding Guo-Lian1,Xu Chen-Ming1,Jiang Shi-Wen23,Huang He-Feng1,Jin Fan1

Affiliation:

1. Department of Reproductive Endocrinology, Women's Hospital, School of Medicine, Zhejiang University, 310006 Hangzhou, China

2. Department of Biomedical Science, Mercer University School of Medicine, Savannah, GA 31499, USA

3. Department of Obstetrics and Gynecology, Mayo Clinic, Rochester, MN 55905, USA

Abstract

In vitro maturation (IVM) of oocyte is an effective procedure for avoiding ovarian hyperstimulation syndrome in patients with polycystic ovaries (PCOS) during in vitro fertilization (IVF). To investigate the influences of IVM on epigenetic reprogramming and to search for the possible reasons for the lower rates of fertilization and cleavage in IVM oocytes, we examined the expression of two enzymes controlling histone acetylation, histone acetyltransferase GCN5 (GCN5) and histone deacetylase 1 (HDAC1), as well as their common target, acetyl-histone H3 (Ac-H3), in mouse metaphase II (MII) oocytes and preimplantation embryos. Results showed that IVM downregulated the protein expression of GCN5 in MII oocytes and two-cell embryos and changed the distribution of GCN5 in two-cell embryos. Expression of HDAC1 mRNA in MII oocytes and two-cell embryos decreased in the IVM group. However, none of these changes persisted after two-cell embryos. Levels of Ac-H3 in both oocytes and embryos remained unchanged after IVM. Our studies indicated that IVM could affect the protein and gene expression related to histone acetylation in oocytes and early cleavage embryos. By function of selection, parts of the changes could be recovered in late embryo development.

Funder

National Basic Research Program of China

Publisher

Hindawi Limited

Subject

Obstetrics and Gynecology

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