Changes in large-scale chromatin structure and function during oogenesis: A journey in company with follicular cells

• Published in: Animal reproduction science Vol. 149; no. 1-2; pp. 3 - 10
• Main Authors: Luciano, Alberto M., Franciosi, Federica, Dieci, Cecilia, Lodde, Valentina
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.09.2014
• Subjects: Animals; biomarkers; breeding; Chromatin; Chromatin - physiology; Chromatin Assembly and Disassembly - physiology; Cumulus cells; DNA methylation; Female; gap junctions; gene expression; genes; Germinal vesicle; health status; histones; human fertility; Humans; mammals; meiosis; Oocyte; oogenesis; Oogenesis - physiology; Ovarian Follicle - cytology; prophase; transcription (genetics); Transcriptional activity; Transcriptome; Chromatin; Germinal vesicle; Transcriptional activity; Oocyte; Transcriptome; Cumulus cells
• ISSN: 0378-4320; 1873-2232; 1873-2232
• DOI: 10.1016/j.anireprosci.2014.06.026

•Chromatin remodeling is a marker of oocyte differentiation and developmental competence.•Chromatin remodeling requires functional GJ communications between oocyte and follicular cells.•GJC functionality affects chromatin remodeling and transcription by cAMP-mediated mechanism(s).•Transcriptome of cumulus cells investment is a tool to gain information on oocyte competence. The mammalian oocyte nucleus or germinal vesicle (GV) exhibits characteristic chromatin configurations, which are subject to dynamic modifications through oogenesis. Aim of this review is to highlight how changes in chromatin configurations are related to both functional and structural modifications occurring in the oocyte nuclear and cytoplasmic compartments. During the long phase of meiotic arrest at the diplotene stage, the chromatin enclosed within the GV is subjected to several levels of regulation. Morphologically, the chromosomes lose their individuality and form a loose chromatin mass. The decondensed configuration of chromatin then undergoes profound rearrangements during the final stages of oocyte growth that are tightly associated with the acquisition of meiotic and developmental competence. Functionally, the discrete stages of chromatin condensation are characterized by different level of transcriptional activity, DNA methylation and covalent histone modifications. Interestingly, the program of chromatin rearrangement is not completely intrinsic to the oocyte, but follicular cells exert their regulatory actions through gap junction mediated communications and intracellular messenger dependent mechanism(s). With this in mind and since oocyte growth mostly relies on the bidirectional interaction with the follicular cells, a connection between cumulus cells gene expression profile and oocyte developmental competence, according to chromatin configuration is proposed. This analysis can help in identifying candidate genes involved in the process of oocyte developmental competence acquisition and in providing non-invasive biomarkers of oocyte health status that can have important implications in treating human infertility as well as managing breeding schemes in domestic mammals.