Abstract

In vitro embryo production success in juvenile animals is compromised due to their intrinsic lower oocyte quality. Conventional in vitro maturation (IVM) impairs oocyte competence by inducing spontaneous meiotic resumption. A series of experiments were performed to determine if maintaining meiotic arrest during a pre-maturation culture phase (pre-IVM) prior to conventional IVM improves oocyte competence of juvenile-goat (2 months old) cumulus-oocyte complexes (COCs). In experiment 1, COCs were cultured with C-type natriuretic peptide (CNP; 0, 50, 100, 200 nM) for 6 and 8 h. Nuclear stage was assessed, revealing no differences in the incidence of germinal vesicle (GV) breakdown. In experiment 2, the same CNP concentrations were assessed plus 10 nM estradiol, the known upstream agonist activating expression of NPR2, the exclusive receptor of CNP. CNP (200 nM) plus estradiol increased the rate of oocytes at GV stage at 6 h compared to control group (74.7% vs 28.3%; P<0.05) with predominantly condensed chromatin configuration. In experiment 3, relative mRNA quantification revealed NPR2 expression was down-regulated after pre-IVM (6 h). In experiment 4, analysis of transzonal projections indicated that pre-IVM maintained cumulus-oocyte communication after oocyte recovery. For experiments 5 and 6, biphasic IVM (6 h pre-IVM with CNP and estradiol, plus 24 h IVM) and control IVM (24 h) were compared. Biphasic IVM increased intra-oocyte glutathione and decreased ROS, up-regulated DNA-methyltransferase 1 and pentraxin 3 expression and led to an increase in rate of blastocyst development compared to control group (30.2% vs 17.2%; P<0.05). In conclusion, a biphasic IVM, including a pre-IVM with CNP, maintains oocyte meiotic arrest for 6 h and enhances the embryo developmental competence of oocytes from juvenile goats.

Highlights

  • Juvenile in vitro embryo transfer (JIVET) has great potential for improving breeding programs as it can increase the rate of genetic gain by reducing the generation interval [1], especially as ovaries from juvenile females provide higher numbers of oocytes than adults [2]

  • In experiment 2, chromatin configuration was assessed after 6 h of pre-in vitro maturation (IVM) (Fig 2)

  • There was a higher rate of oocytes at germinal vesicle (GV) stage with condensed clumped chromatin in the 200 nM C-type natriuretic peptide (CNP) + E2 group compared to control group (P

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Summary

Introduction

Juvenile in vitro embryo transfer (JIVET) has great potential for improving breeding programs as it can increase the rate of genetic gain by reducing the generation interval [1], especially as ovaries from juvenile females provide higher numbers of oocytes than adults [2]. Oocytes retrieved from small follicles (< 3 mm) developed to the blastocyst stage at a lower rate than oocytes from adult females (reviewed by Paramio & Izquierdo [3]). Oocyte in vitro maturation (IVM) is a limiting step for in vitro embryo production (IVEP). Conventional IVM impairs oocyte competence (the ability to sustain embryo development and lead a pregnancy to term [4]). Competence acquisition depends on changes at nuclear and cytoplasmic levels that occur during folliculogenesis prior to final oocyte maturation (reviewed by Gilchrist & Thompson [5]). Oocytes spontaneously resume meiosis in vitro following retrieval from antral follicles [6], which prevents the oocyte to fulfill this process

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