首页> 外文期刊>Fertility and Sterility: Official Journal of the American Fertility Society, Pacific Coast Fertility Society, and the Canadian Fertility and Andrology Society >Age-associated alteration of oocyte-specific gene expression in polar bodies: Potential markers of oocyte competence
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Age-associated alteration of oocyte-specific gene expression in polar bodies: Potential markers of oocyte competence

机译:年龄相关的极体卵母细胞特异性基因表达的改变:卵母细胞能力的潜在标志

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Objective: To confirm that oocyte-specific messenger RNAs are detectable in the polar body (PB) of metaphase II (MII) oocytes and determine the effect of age on oocyte-specific transcript levels. Design: Prospective study. Setting: Hospital-based academic research laboratory. Animal(s): CD1 female mice. Intervention(s): Aged (40-50 weeks) and young (7-9 weeks) mice were administered pregnant mare serum gonadotropin (PMSG) and hCG. Oocytes were fertilized in vitro to assess fertilization and developmental competence. The MII oocytes were obtained and first PBs were removed. Messenger RNAs from each PB and its sibling oocyte were reverse transcribed and analyzed by real-time quantitative polymerase chain reaction (PCR). Main Outcome Measure(s): Fertilization and developmental rates and expression of six oocyte-specific genes (Bmp15, Gdf9, H1foo, Nlrp5, Tcl1, and Zp3) in PBs and sibling oocytes from young versus aged mice. Result(s): Oocytes from aged mice had lower developmental competence. Four genes (H1foo, Nlrp5, Tcl1, and Zp3) were differentially expressed in aged versus young oocytes. All six transcripts were present in PBs from aged and young mice at lower levels than in the sibling oocytes; transcript levels were lower in aged PBs compared with young PBs. Conclusion(s): There is a significant difference in the transcript levels of oocyte-specific genes in aged versus young PB that correlates with age-related decreases in oocyte competence. Differences in gene expression in PB may be potential biomarkers of MII oocyte competence.
机译:目的:确认卵母细胞特异性信使RNAs在中期II(MII)卵母细胞的极体(PB)中可检测到,并确定年龄对卵母细胞特异性转录本水平的影响。设计:前瞻性研究。地点:基于医院的学术研究实验室。动物:CD1雌性小鼠。干预措施:给老年(40-50周)和幼年(7-9周)的小鼠注射母马血清促性腺激素(PMSG)和hCG。卵母细胞体外受精,以评估受精和发育能力。获得了MII卵母细胞并去除了第一个PB。来自每个PB及其兄弟卵母细胞的Messenger RNA进行逆转录,并通过实时定量聚合酶链反应(PCR)进行分析。主要观察指标:受精和发育率以及六个卵母细胞特异性基因(Bmp15,Gdf9,H1foo,Nlrp5,Tcl1和Zp3)在PB和同龄和老年小鼠的同卵卵母细胞中的表达。结果:衰老小鼠的卵母细胞发育能力较低。四个基因(H1foo,Nlrp5,Tcl1和Zp3)在老年卵母细胞和年轻卵母细胞中差异表达。所有六种转录本均以同胞卵母细胞中较低的水平存在于成年和幼年小鼠的PB中。老年PB的转录水平低于年轻PB。结论:老年和年轻PB中卵母细胞特异性基因的转录水平存在显着差异,这与年龄相关的卵母细胞能力下降有关。 PB中基因表达的差异可能是MII卵母细胞能力的潜在生物标志物。

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