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Extended In Vitro Maturation Enhances Oocyte Developmental Competence but Alters Gene Expression in Bovine Embryos
Thomas Chia-Tang Ho1, Takashi Tanida2, Takashi Fujii3
1Laboratory of Theriogenology, Graduate School of Veterinary Science, Osaka Metropolitan University, Izumisano, Japan.
Molecular Reproduction and Development
|November 19, 2025
Summary
Extending in vitro maturation (IVM) to 28 hours improves bovine oocyte development, especially for slow nuclear maturation speed (NMS) oocytes. However, longer IVM reduces pluripotency gene expression, impacting embryo quality.
Area of Science:
- Veterinary Science
- Reproductive Biology
- Biotechnology
Background:
- In vitro maturation (IVM) is crucial for bovine oocyte development.
- Nuclear maturation speed (NMS) varies among oocytes, affecting developmental potential.
- Machine learning can predict NMS, enabling tailored IVM protocols.
Purpose of the Study:
- To determine the optimal IVM duration for bovine oocytes based on predicted NMS.
- To assess the impact of IVM duration on oocyte developmental competence and embryo quality.
- To correlate IVM duration with gene expression in resulting blastocysts.
Main Methods:
- Machine learning was used to classify bovine oocytes into fast- or slow-predicted NMS groups.
- Oocytes were subjected to IVM for 24, 28, or 32 hours.
- Developmental competence (cleavage, blastocyst formation) and embryo quality (gene expression) were evaluated.
Main Results:
- Extending IVM to 28 hours significantly improved cleavage rates and accelerated first cleavage timing in slow NMS oocytes.
- Blastocyst formation rates for slow NMS oocytes matured for 24 hours improved to levels comparable to fast NMS oocytes at 28 hours IVM.
- Extended IVM (28 and 32 hours) decreased the expression of pluripotency genes (NANOG, OCT4) in blastocysts, irrespective of NMS.
Conclusions:
- A 28-hour IVM duration enhances the developmental competence of slow NMS bovine oocytes.
- Optimizing IVM duration based on predicted NMS is key for efficient bovine embryo production.
- While improving developmental rates, extended IVM may compromise embryonic developmental potential by reducing pluripotency gene expression.

