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HDAC3 inhibition disrupts the assembly of meiotic apparatus during porcine oocyte maturation.

Ling GuXiaoyan LiXiaohui LiuMin GaoYongfu HeBo XiongHonglin Liu
Published in: Journal of cellular physiology (2018)
Histone deacetylases (HDACs) are involved in a wide array of biological processes. However, the role of HDAC3 in porcine oocytes remains unclear. In the current study, we examine the effects of HDAC3 inhibition on porcine oocyte maturation using RGFP966, a selective HDAC3 inhibitor. We find that suppression of HDAC3 activity prevents not only the expansion of cumulus cells but also the meiotic progression of oocytes. It is interesting to note that HDAC3 displays a spindle-like distribution pattern as the porcine oocytes enter meiosis. In line with this, confocal microscopy reveals the high frequency of spindle defects and chromosomal congression failure in metaphase oocytes exposed to RGFP966. Moreover, HDAC3 inhibition results in the hyperacetylation of α-tubulin during oocyte meiosis. These findings indicate that HDAC3 activity might control the microtubule stability via the deacetylation of tubulin, which is critical for maintaining the proper spindle assembly, accurate chromosome separation, and orderly meiotic progression during porcine oocyte maturation.
Keyphrases
  • histone deacetylase
  • high frequency
  • dna methylation
  • copy number
  • oxidative stress
  • cell proliferation
  • mass spectrometry