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.

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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