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Updated: Oct 12, 2025

Author Spotlight: Understanding DNA Damage Response in Mammalian Oocytes and Preimplantation Embryos
Published on: June 23, 2023
DNA damage repair is suppressed in porcine aged oocytes
Tao Lin1,2, Ling Sun1,2, Jae Eun Lee2
1School of Life Sciences and Food Engineering, Hebei University of Engineering, Handan 056038, China.
Abstract:
This study sought to evaluate DNA damage and repair in porcine postovulatory aged oocytes. The DNA damage response, which was assessed by H2A.X expression, increased in porcine aged oocytes over time. However, the aged oocytes exhibited a significant decrease in the expression of RAD51, which reflects the DNA damage repair capacity. Further experiments suggested that the DNA repair ability was suppressed by the downregulation of genes involved in the homologous recombination (HR) and nonhomologous end-joining (NHEJ) pathways. The expression levels of the cell cycle checkpoint genes, CHEK1 and CHEK2, were upregulated in porcine aged oocytes in response to induced DNA damage. Immunofluorescence results revealed that the expression level of H3K79me2 was significantly lower in porcine aged oocytes than in control oocytes. In addition, embryo quality was significantly reduced in aged oocytes, as assessed by measuring the cell proliferation capacity. Our results provide evidence that DNA damage is increased and the DNA repair ability is suppressed in porcine aged oocytes. These findings increase our understanding of the events that occur during postovulatory oocyte aging.
Insights
Aging porcine oocytes accumulate DNA damage and show reduced DNA repair capacity. This is linked to decreased homologous recombination and nonhomologous end-joining pathway gene expression, impacting embryo quality.
Area of Science:
- Reproductive Biology
- Molecular Biology
- Genetics
Background:
- Oocyte aging is a significant factor affecting female fertility.
- Understanding the molecular mechanisms underlying oocyte aging is crucial for reproductive health.
Purpose of the Study:
- To investigate DNA damage and repair mechanisms in postovulatory aged porcine oocytes.
- To elucidate the impact of aging on DNA repair pathways and subsequent oocyte quality.
Main Methods:
- Assessed DNA damage via H2A.X expression.
- Evaluated DNA repair capacity by measuring RAD51 expression.
- Analyzed gene expression in homologous recombination (HR) and nonhomologous end-joining (NHEJ) pathways.
- Quantified cell cycle checkpoint gene expression (CHEK1, CHEK2).
- Measured H3K79me2 levels using immunofluorescence.
- Assessed embryo quality by cell proliferation capacity.
Main Results:
- Increased DNA damage response (H2A.X expression) in aged porcine oocytes.
- Decreased DNA damage repair capacity (RAD51 expression) in aged oocytes.
- Downregulation of HR and NHEJ pathway genes, suppressing DNA repair.
- Upregulation of cell cycle checkpoint genes (CHEK1, CHEK2) in response to DNA damage.
- Reduced H3K79me2 levels in aged oocytes.
- Significantly reduced embryo quality in aged oocytes.
Conclusions:
- Postovulatory aging in porcine oocytes leads to increased DNA damage.
- DNA repair ability is suppressed in aged oocytes due to impaired HR and NHEJ pathways.
- Oocyte aging negatively impacts embryo development and quality.
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