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首页> 外文期刊>The Journal of Reproduction and Development >The possibility of a false positive arising from sperm DNA in genetic diagnosis of bovine embryos.
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The possibility of a false positive arising from sperm DNA in genetic diagnosis of bovine embryos.

机译:在牛胚胎的基因诊断中,精子DNA产生假阳性的可能性。

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摘要

The present study was conducted to evaluate the effect of accessory sperm cells that adhered to the zona pellucida or blastomeres on the accuracy of genetic diagnosis of preimplantation embryos. The properties of sperm cells as a template for DNA amplification were examined using bovine sperm cells frozen-thawed or incubated in PBS after thawing for 7 days at 39 C. Sexing by loop-mediated isothermal amplification (LAMP) and claudin-16 genotyping by polymerase chain reaction (PCR) were performed using 10, 50 and 100 sperm cells. When sexing based on LAMP was performed, no amplified DNA was detected in 10 sperm-derived samples, whereas male-specific (10-60%) and gender-natural DNA (30-100%) sequences were detected in 50 and 100 sperm-derived samples. The detection rates for gender-natural DNA sequences were higher in incubated sperm samples than in sperm samples immediately after freeze-thawing. The detection rates for claudin-16 were low (7-13%) regardless of the concentration of sperm cells and the period of incubation after thawing. The present results showed that male-specific DNA, gender-natural DNA and claudin-16 sequences were not usually amplified from a small number of sperm cells (< or =10 cells). However, when a large number of sperm cells (> or =50 cells) were present, male-specific and gender-natural DNA sequences were amplified at a high rate, and claudin-16 DNA sequences were also occasionally detected. These results raise the possibility that accessory sperm cells may reduce the accuracy of the genetic diagnosis of bovine embryos. Therefore, steps to prevent the contamination of sperm cells, such as removal of the zona pellucida and washing of sample blastomeres, are necessary to obtain an accurate result.
机译:本研究旨在评估附着在透明带或卵裂球上的辅助精子细胞对植入前胚胎遗传诊断准确性的影响。在39°C解冻7天后,使用冻融或在PBS中孵育的牛精子细胞检查作为DNA扩增模板的精子细胞的特性。通过环介导的等温扩增(LAMP)进行性别鉴定和通过聚合酶进行claudin-16基因分型。使用10、50和100个精子细胞进行链反应(PCR)。当基于LAMP进行性别鉴定时,在10个精子来源的样品中未检测到扩增的DNA,而在50个精子和100个精子中检测到了男性特异性(10-60%)和性别自然的DNA(30-100%)序列。衍生样本。孵育后的精子样品中的性别天然DNA序列的检出率要比冻融后立即的精子样品中的更高。无论精子细胞的浓度和解冻后的培养时间长短,claudin-16的检出率均较低(7-13%)。目前的结果表明,通常不从少数精子细胞(<或= 10个细胞)中扩增出雄性特异性DNA,性别天然DNA和claudin-16序列。但是,当存在大量的精子细胞(>或= 50个细胞)时,雄性特异性和性别天然的DNA序列会被高速扩增,并且偶尔还会检测到claudin-16 DNA序列。这些结果增加了辅助精子细胞可能降低牛胚胎遗传诊断准确性的可能性。因此,为了获得准确的结果,必须采取防止精子细胞污染的步骤,例如去除透明带和清洗卵裂球样品。

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