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Concurrent Measurement of Mitochondrial DNA Copy Number and ATP Concentration in Single Bovine Oocytes

机译:单牛卵母细胞中的线粒体DNA拷贝数和ATP浓度的同时测量

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To sustain energy-demanding developmental processes, oocytes must accumulate adequate stores of metabolic substrates and mitochondrial numbers prior to the initiation of maturation. In the past, researchers have utilized pooled samples to study oocyte metabolism, and studies that related multiple metabolic outcomes in single oocytes, such as ATP concentration and mitochondrial DNA copy number, were not possible. Such scenarios decreased sensitivity to intraoocyte metabolic relationships and made it difficult to obtain adequate sample numbers during studies with limited oocyte availability. Therefore, we developed and validated procedures to measure both mitochondrial DNA (mtDNA) copy number and ATP quantity in single oocytes. Validation of our procedures revealed that we could successfully divide oocyte lysates into quarters and measure consistent results from each of the aliquots for both ATP and mtDNA copy number. Coefficient of variation between the values retrieved for mtDNA copy number and ATP quantity quadruplicates were 4.72 ± 0.98 and 1.61 ± 1.19, respectively. We then utilized our methodology to concurrently measure mtDNA copy number and ATP quantity in germinal vesicle (GV) and metaphase two (MII) stage oocytes. Our methods revealed a significant increase in ATP levels (GV = 628.02 ± 199.53 pg, MII = 1326.24 ± 199.86 pg, p 0.001) and mtDNA copy number (GV = 490,799.4 ± 544,745.9 copies, MII = 1,087,126.9 ± 902,202.8 copies, p = 0.035) in MII compared to GV stage oocytes. This finding is consistent with published literature and provides further validation of the accuracy of our methods. The ability to produce consistent readings and expected results from aliquots of the lysate from a single oocyte reveals the sensitivity and feasibility of using this method.
机译:为了维持能量苛刻的发育过程,卵母细胞必须在开始成熟之前积累代谢底物和线粒体数的足够储存。在过去,研究人员利用汇集的样品来研究卵母细胞代谢,并且不可能研究单一卵母细胞中的多种代谢结果,例如ATP浓度和线粒体DNA拷贝数。这种情景降低了对胃癌代谢关系的敏感性,并使在具有有限的卵母细胞可用性的研究期间难以获得适当的样品数。因此,我们开发和经过验证的程序,以测量单卵母细胞中的线粒体DNA(MTDNA)拷贝数和ATP量。验证我们的程序揭示我们可以成功将卵母细胞裂解物分为季度,并测量ATP和MTDNA拷贝数的每种等分试样的一致结果。检索MTDNA拷贝数和ATP量四分单位的值之间的变化系数分别为4.72±0.98和1.61±1.19。然后我们利用我们的方法来同时测量发芽囊泡(GV)和中期卵囊中的MTDNA拷贝数和ATP数量和中期卵母细胞。我们的方法揭示了ATP水平的显着增加(GV = 628.02±199.53 pg,MII = 1326.24±199.86 pg,P <0.001)和MTDNA拷贝数(GV = 490,799.4±544,745.9拷贝,MII = 1,087,126.9±902,202.8份,P =与GV阶段卵母细胞相比,在MII中为0.035)。这一发现与已发表的文献一致,并进一步验证了我们的方法的准确性。从单个卵母细胞的裂解物的等分试样产生一致读数和预期结果的能力揭示了使用该方法的敏感性和可行性。

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