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Nucleolar Translocation of Histone Deacetylase 2 Is Involved in Regulation of Transcriptional Silencing in the Cat Germinal Vesicle

机译:组蛋白脱乙酰基酶2的核易位参与调节猫萌发囊泡中的转录沉默。

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摘要

Histone deacetylase 2 (HDAC2) is a key transcriptional coregulator that is suspected to play a role during oogenesis. It is known that RNA transcription in the cat germinal vesicle (GV) stops during folliculogenesis at the late antral follicle stage and is unrelated to histone deacetylation or chromatin condensation. The objective of the present study was to determine if and how HDAC2 participates in transcription regulation in the cat GV. Spatiotemporal HDAC2 protein expression was examined by immunostaining oocytes from primary to large antral follicles. HDAC2 was detected in the majority of GVs within oocytes from early, small, and large antral follicles. At early and small antral stages, HDAC2 was found primarily in the GV's nucleoplasm. There then was a significant shift in HDAC2 localization into the nucleolus, mostly in oocytes from large antral follicles. Assessments revealed that transcription was active in oocytes that contained nucleoplasm-localized HDAC2, whereas nucleolar-bound HDAC2 was associated with loss of both global transcription and ribosomal RNA presence at all antral stages. When oocytes were exposed to the HDAC inhibitor valproic acid, results indicated that HDAC regulated transcriptional activity in the nucleoplasm, but not in the nucleolus. Collective results suggest that nucleolar translocation of HDAC2 is associated with transcriptional silencing in the GV, thereby likely contributing to an oocyte's acquisition of competence.
机译:组蛋白脱乙酰基酶2(HDAC2)是关键的转录共调节因子,被怀疑在卵子发生过程中起作用。众所周知,猫生小囊泡(GV)中的RNA转录在窦房毛囊晚期的卵泡形成过程中停止,并且与组蛋白脱乙酰化或染色质浓缩无关。本研究的目的是确定HDAC2是否以及如何参与猫GV中的转录调控。时空HDAC2蛋白表达通过从原发性卵泡到大型肛门卵泡的卵母细胞进行免疫染色进行检查。在早期,小型和大型肛门卵泡的卵母细胞中,大多数GV中均检测到HDAC2。在早期和小的肛门期,HDAC2主要在GV的核质中发现。然后,HDAC2的定位发生了显着变化,进入核仁,主要是来自大型肛门卵泡的卵母细胞。评估显示,转录在含有核质定位的HDAC2的卵母细胞中是活跃的,而与核仁结合的HDAC2与在所有肛门期的整体转录和核糖体RNA的存在都减少有关。当卵母细胞暴露于HDAC抑制剂丙戊酸时,结果表明HDAC调节核质而不是核仁的转录活性。集体的结果表明,HDAC2的核仁移位与GV中的转录沉默有关,从而可能有助于卵母细胞的能力获得。

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