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Protein Phosphatase 6 Protects Prophase I-Arrested Oocytes by Safeguarding Genomic Integrity

机译:蛋白磷酸酶6通过保护基因组完整性保护前期I捕集的卵母细胞

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摘要

Mammalian oocytes are arrested at prophase of the first meiotic division in the primordial follicle pool for months, even years, after birth depending on species, and only a limited number of oocytes resume meiosis, complete maturation, and ovulate with each reproductive cycle. We recently reported that protein phosphatase 6 (PP6), a member of the PP2A-like subfamily, which accounts for cellular serine/threonine phosphatase activity, functions in completing the second meiosis. Here, we generated mutant mice with a specific deletion of Ppp6c in oocytes from the primordial follicle stage by crossing Ppp6cF/F mice with Gdf9-Cre mice and found that Ppp6cF/F; GCre+ mice are infertile. Depletion of PP6c caused folliculogenesis defects and germ cell loss independent of the traditional AKT/mTOR pathway, but due to persistent phosphorylation of H2AX (a marker of double strand breaks), increased susceptibility to DNA damage and defective DNA repair, which led to massive oocyte elimination and eventually premature ovarian failure (POF). Our findings uncover an important role for PP6 as an indispensable guardian of genomic integrity of the lengthy prophase I oocyte arrest, maintenance of primordial follicle pool, and thus female fertility.
机译:哺乳动物卵母细胞在出生后的第一代减数分裂分裂前期被捕,取决于种类,数月甚至数年,只有有限数量的卵母细胞恢复减数分裂,完全成熟并在每个生殖周期排卵。我们最近报道蛋白质磷酸酶6(PP6),PP2A样亚科的成员,占细胞丝氨酸/苏氨酸磷酸酶活性,在完成第二次减数分裂中起作用。在这里,我们通过将Ppp6c F / F 小鼠与Gdf9-Cre小鼠杂交,从原始卵泡期的卵母细胞中产生了具有Ppp6c特异性缺失的突变小鼠,并发现Ppp6c F / F ; GCre +小鼠不育。 PP6c的消耗导致卵泡发生缺陷和生殖细胞损失,而与传统的AKT / mTOR途径无关,但由于H2AX的持续磷酸化(双链断裂的标志),对DNA损伤的敏感性增加和DNA修复缺陷,导致卵母细胞大量增多消除并最终导致卵巢早衰(POF)。我们的发现揭示了PP6作为长期前期I卵母细胞停滞,原始卵泡池维持以及女性生育能力的基因组完整性必不可少的保护者。

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