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The activity and copy number of mitochondrial DNA in ovine oocytes throughout oogenesis in vivo and during oocyte maturation in vitro

机译:整个卵子生成过程中以及体外卵母细胞成熟过程中绵羊卵母细胞中线粒体DNA的活性和拷贝数

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摘要

Mitochondria are responsible for the production of ATP, which drives cellular metabolic and biosynthetic processes. This is the first study to quantify the mtDNA copy number across all stages of oogenesis in a large monovulatory species, it includes assessment of the activity of mitochondria in germinal vesicle (GV) and metaphase II (MII) oocytes through JC1 staining. Primordial to early antral follicles (n = 249) were isolated from the sheep ovarian cortex following digestion at 37°C for 1 h and all oocytes were disaggregated from their somatic cells. Germinal vesicle oocytes (n = 133) were aspirated from 3- to 5-mm diameter antral follicles, and mature MII oocytes (n = 71) were generated following in vitro maturation (IVM). The mtDNA copy number in each oocyte was quantified using real-time PCR and showed a progressive, but variable increase in the amount of mtDNA in oocytes from primordial follicles (605 ± 205, n = 8) to mature MII oocytes (744 633 ± 115 799, n = 13; P < 0.05). Mitochondrial activity (P > 0.05) was not altered during meiotic progression from GV to MII during IVM. The observed increase in the mtDNA copy number across oogenesis reflects the changing ATP demands needed to orchestrate cytoskeletal and cytoplasmic reorganization during oocyte growth and maturation and the need to fuel the resumption of meiosis in mature oocytes following the pre-ovulatory gonadotrophin surge.
机译:线粒体负责ATP的产生,该ATP驱动细胞的代谢和生物合成过程。这是第一个量化大型单控物种在卵子发生各个阶段的mtDNA拷贝数的研究,其中包括通过JC1染色评估生小泡(GV)和中期II(MII)卵母细胞中线粒体的活性。在37°C消化1 h后,从绵羊卵巢皮质分离出原始至早期的肛门卵泡(n = 249),并将所有卵母细胞从体细胞中分解。从直径3到5毫米的肛门卵泡中抽吸出胚泡卵母细胞(n = 133),并在体外成熟(IVM)后生成成熟的MII卵母细胞(n = 71)。使用实时PCR定量每个卵母细胞中mtDNA的拷贝数,并显示从原始卵泡(605±205,n = 8)到成熟MII卵母细胞(744 633±115)的卵母细胞中mtDNA的数量逐渐增加,但变化不定799,n = 13; P <0.05)。在IVM期间,从GV到MII的减数分裂进程中,线粒体活性(P> 0.05)没有改变。观察到的整个卵子发生过程中mtDNA拷贝数的增加反映了在卵母细胞生长和成熟过程中协调细胞骨架和细胞质重组所需的ATP需求变化,以及排卵前促性腺激素激增后成熟卵母细胞恢复减数分裂的需求。

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