Li Huifang, Hu Yan, Song Chi, Ji Gaige, Liu Hongxiang, Xu Wenjuan, Ding Jing
Jiangsu Provincial Key Laboratory of Poultry Genetics & Breeding, Institute of Poultry Science of Jiangsu Province, Yangzhou, PR China.
Sex Dev. 2015;9(3):173-81. doi: 10.1159/000381075. Epub 2015 Apr 17.
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 invasive, had no adverse effects on either embryos or the post-hatching survival of young ducks and could be used in developmental biology research in birds.
在鸭的早期孵化期,即胚胎发育的第1天到第13天,精确鉴定性别可能会比较困难。在一项初步试验中,我们发现用于基于PCR的检测以鉴定鸭性别时,经典的用于解旋酶DNA结合蛋白1基因(CHD1)的P2/P8、1237L/1272H和2550F/2718R引物存在缺陷。因此,设计了用于鸭性别鉴定的通用PCR引物HPF/HPR。对PCR产物进行克隆、测序,并使用GenBank进行分析。使用成年鸟类的血液和羽毛样本以及胚胎的绒毛尿囊膜和尿囊液(AF)作为DNA来源,比较了引物的有效性。495bp的CHD1-Z和351bp的CHD1-W PCR扩增产物在3%的琼脂糖凝胶上很容易区分,雌性(ZW)显示出两条可见带,而雄性(ZZ)只发现一条带。结果表明,HPF/HPR引物比用于鸭性别鉴定的经典引物效率更高、更可靠。在设计新引物的过程中,建立了一种从自由生活的鸟类中收集极少量AF的采样技术。这种技术微创,对胚胎或幼鸭孵化后的存活均无不良影响,可用于鸟类发育生物学研究。