首页> 外文期刊>Sexual development: genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation >A New Primer for Sex Identification of Ducks and a Minimally Invasive Technique for Sampling of Allantoic Fluid to Detect Sex during Bird Embryo Development
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A New Primer for Sex Identification of Ducks and a Minimally Invasive Technique for Sampling of Allantoic Fluid to Detect Sex during Bird Embryo Development

机译:一种新的鸭性别鉴定引物和一种用于尿囊液的微创采样技术,以检测鸟类胚胎发育过程中的性别

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During the early incubation period of the duck, from embryonic day 1 to 13, a precise identification of the sex may be difficult. In a preliminary test, we found a defect in the use of the classical P2/P8, 1237L/1272H, and 2550F/2718R primers for chromo-helicase-DNA-binding 1 gene (CHD1) as a PCR-based test to identify sex in ducks. Therefore, universal PCR primers HPF/HPR for sexing ducks were designed. The PCR product was cloned, sequenced, and analyzed using GenBank. The effectiveness of the primers was compared using samples of blood and feathers from adult birds and chorioallantoic membranes and allantoic fluid (AF) of embryos as a source of DNA. The 495-bp CHD1-Z and the 351-bp CHD1-W PCR amplicons could be easily distinguished on a 3% agarose gel, and females (ZW) displayed 2 visible bands whereas only a single band was found in males (ZZ). The results indicated that HPF/HPR primers were highly efficient and more reliable than the classical primers used for sexing ducks. During the design of the new primers, an AF sampling technique was established to collect a very small amount of AF from free-living birds. This technique, which was minimally inva- sive, had no adverse effects on either embryos or the posthatching survival of young ducks and could be used in developmental biology research in birds. (C) 2015 S. Karger AG, Basel
机译:在鸭子的早期潜伏期(从胚胎的第1天到第13天),可能很难准确识别性别。在初步测试中,我们发现将经典P2 / P8、1237L / 1272H和2550F / 2718R引物用于染色体-helasease-DNA结合1基因(CHD1)的缺陷,无法用作基于PCR的鉴定性别的试验在鸭子里。因此,设计了用于野鸭的通用PCR引物HPF / HPR。使用GenBank克隆,测序和分析PCR产物。使用成年鸟类的血液和羽毛样本以及绒毛尿囊膜和胚胎的尿囊液(AF)作为DNA来源,比较了引物的有效性。 495 bp CHD1-Z和351 bp CHD1-W PCR扩增子可在3%琼脂糖凝胶上轻松区分,雌性(ZW)显示2条可见条带,而雄性(ZZ)仅发现一条条带。结果表明,HPF / HPR引物比用于鸭性别鉴定的经典引物更高效,更可靠。在设计新引物的过程中,建立了一种AF采样技术以从自由活动的禽类中收集非常少量的AF。这种技术具有最小的侵入性,对胚胎或幼鸭的孵化后存活均无不利影响,可用于鸟类的发育生物学研究。 (C)2015 S.Karger AG,巴塞尔

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