The Histone Deacetylase Inhibitor Trichostatin A Induces Retrogressive Chromatin Decondensation in the Germinal Vesicle of Porcine Cumulus-enclosed Oocytes

Y. Hirao, N. Takenouchi, M. Shimizu, K. Iga, T. Miyano, T. Nagai
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Abstract

In porcine growing oocytes, chromatin remains diffuse. As the oocytes approach their final size, 120 μm, the chromatin becomes partly condensed and forms a perinucleolar sheath. These changes occur simultaneously with a decrease in transcriptional activity. In many other cell types, it has been shown that the state of acetylation of nucleosome core histones is essential in chromatin remodeling and transcription so that partial chromatin condensation in oocytes may involve the recruitment of histone deacetylases. In order to test this hypothesis, porcine oocyte-cumulus cell complexes were treated with a specific inhibitor of histone deacetylases, trichostatin A (TSA). The perinucleolar sheath loosened or disappeared after 24 hr culture with 100 nM TSA, but after further culture in TSA-free medium, about 40% developed the perinucleolar sheath again. In the presence of 4 mM hypoxanthine, the decondensation induced by TSA progressed rather slowly, but continuously, for 72 hr. When oocytes were denuded before culture, spontaneous maturation occurred in the presence of TSA. Thus, the inhibitor-induced decondensation is not attributed to the inhibition of the maturation-promoting factor. These results suggest that deacetylation of histones may be involved in chromatin remodeling in oocytes near the end of the growth phase.
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组蛋白去乙酰化酶抑制剂曲古霉素A诱导猪卵母细胞生发囊中染色质退行性去浓缩
在生长中的猪卵母细胞中,染色质仍然是弥散的。当卵母细胞接近其最终大小(120 μm)时,染色质部分浓缩并形成核周鞘。这些变化与转录活性的降低同时发生。在许多其他细胞类型中,研究表明核小体核心组蛋白的乙酰化状态在染色质重塑和转录中是必不可少的,因此卵母细胞中部分染色质凝聚可能涉及组蛋白去乙酰化酶的募集。为了验证这一假设,用特异性组蛋白去乙酰化酶抑制剂曲古霉素a (TSA)处理猪卵母细胞-卵丘细胞复合物。100 nM TSA培养24小时后,核周鞘松动或消失,但在无TSA培养基中进一步培养后,约40%的核周鞘重新发育。在4 mM次黄嘌呤存在的情况下,TSA诱导的去浓缩进展缓慢,但持续72小时。在培养前剥去卵母细胞,在TSA存在下发生自发成熟。因此,抑制剂诱导的去致密化不能归因于成熟促进因子的抑制。这些结果表明,组蛋白的去乙酰化可能参与了卵母细胞生长末期染色质重塑。
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