Supplementation with serine-enriched non-essential amino acids from minimum essential medium promotes blastocyst development of in vitro-fertilized bovine embryos.

J Reprod Dev

Division of Dairy Cattle Feeding and Breeding Research, Institute of Livestock and Grassland Science, National Agriculture and Food Research Organization, Ibaraki, 305-0901, Japan.

Published: December 2024

AI Article Synopsis

  • To produce high-quality embryos, it's crucial to meet a set of four criteria related to early development and embryo shape.
  • Non-essential amino acids, particularly serine, are vital in the culture of bovine embryos; higher concentrations of serine (1,000 µM) significantly boost the formation of compliant blastocysts compared to the standard 100 µM.
  • The increase in serine aids in DNA methylation processes essential for embryo growth, while inhibiting serine metabolism leads to fewer methyl donors and reduced blastocyst formation.

Article Abstract

To produce an embryo, a high conception rate must be complied along with four evaluation criteria based on the timing of early cleavage and proper embryo morphology (hereafter, these blastocysts will be referred to as "four-criteria-compliant blastocysts"). Therefore, it is necessary to construct a culture system for high efficiency production of embryos meeting these four criteria. Non-essential amino acids (NEAAs) are widely used for the culture of bovine embryos fertilized in vitro; however, the necessity and optimal concentration of individual NEAA must be verified to produce four-criteria-compliant blastocysts. DNA methylation is a critical event for blastocyst formation in bovines, and serine is a common NEAA that serves as a methyl donor and participates in DNA methylation. Serine is generally added at a concentration of 100 µM in bovine embryo culture medium. However, the rate of formation of four-criteria-compliant blastocysts was significantly improved when 1,000 µM of serine was added. Analysis of endogenous serine synthases gene expression in oocytes and embryos revealed that phosphoglycerate dehydrogenase, the rate-limiting enzyme in the serine synthesis pathway, is expressed at the morula stage and beyond. The addition of serine at 1,000 µM increased the amount of methyl donors; moreover, the addition of an inhibitor of serine-metabolizing enzymes decreased the number of methyl donors and markedly inhibited blastocyst formation. These results indicate that the addition of serine at an optimal concentration of 1,000 µM favors production of four-criteria-compliant blastocysts, and that methyl donor synthesis may be involved in this effect.

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Source
http://dx.doi.org/10.1262/jrd.2024-090DOI Listing

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Supplementation with serine-enriched non-essential amino acids from minimum essential medium promotes blastocyst development of in vitro-fertilized bovine embryos.

J Reprod Dev

December 2024

Division of Dairy Cattle Feeding and Breeding Research, Institute of Livestock and Grassland Science, National Agriculture and Food Research Organization, Ibaraki, 305-0901, Japan.

Article Synopsis
  • To produce high-quality embryos, it's crucial to meet a set of four criteria related to early development and embryo shape.
  • Non-essential amino acids, particularly serine, are vital in the culture of bovine embryos; higher concentrations of serine (1,000 µM) significantly boost the formation of compliant blastocysts compared to the standard 100 µM.
  • The increase in serine aids in DNA methylation processes essential for embryo growth, while inhibiting serine metabolism leads to fewer methyl donors and reduced blastocyst formation.
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Embryonic transfer of bovine blastocysts produced by in vitro fertilization is widely utilized-despite a compromised conception rate. It has been suggested that a set of four evaluation criteria for judging the quality of embryos, based on the timing of early cleavages and proper morphologies of embryos, can effectively predict pregnancy success. These blastocysts are hereafter referred to as four-criteria-compliant blastocysts.

View Article and Find Full Text PDF

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