Chang Hsueh-Wei, Cheng Chun-An, Gu De-Leung, Chang Chia-Che, Su San-Hua, Wen Cheng-Hao, Chou Yii-Cheng, Chou Ta-Ching, Yao Cheng-Te, Tsai Chi-Li, Cheng Chien-Chung
Faculty of Biomedical Science and Environmental Biology, Kaohsiung Medical University, Kaohsiung, Taiwan.
BMC Biotechnol. 2008 Feb 12;8:12. doi: 10.1186/1472-6750-8-12.
Combination of CHD (chromo-helicase-DNA binding protein)-specific polymerase chain reaction (PCR) with electrophoresis (PCR/electrophoresis) is the most common avian molecular sexing technique but it is lab-intensive and gel-required. Gender determination often fails when the difference in length between the PCR products of CHD-Z and CHD-W genes is too short to be resolved.
Here, we are the first to introduce a PCR-melting curve analysis (PCR/MCA) to identify the gender of birds by genomic DNA, which is gel-free, quick, and inexpensive. Spilornis cheela hoya (S. c. hoya) and Pycnonotus sinensis (P. sinensis) were used to illustrate this novel molecular sexing technique. The difference in the length of CHD genes in S. c. hoya and P. sinensis is 13-, and 52-bp, respectively. Using Griffiths' P2/P8 primers, molecular sexing failed both in PCR/electrophoresis of S. c. hoya and in PCR/MCA of S. c. hoya and P. sinensis. In contrast, we redesigned sex-specific primers to yield 185- and 112-bp PCR products for the CHD-Z and CHD-W genes of S. c. hoya, respectively, using PCR/MCA. Using this specific primer set, at least 13 samples of S. c. hoya were examined simultaneously and the Tm peaks of CHD-Z and CHD-W PCR products were distinguished.
In this study, we introduced a high-throughput avian molecular sexing technique and successfully applied it to two species. This new method holds a great potential for use in high throughput sexing of other avian species, as well.
将CHD(染色体解旋酶-DNA结合蛋白)特异性聚合酶链反应(PCR)与电泳相结合(PCR/电泳)是最常用的鸟类分子性别鉴定技术,但该技术需要大量实验操作且依赖凝胶。当CHD-Z和CHD-W基因的PCR产物长度差异过短而无法分辨时,性别鉴定往往会失败。
在此,我们首次引入了一种PCR熔解曲线分析(PCR/MCA)方法,通过基因组DNA鉴定鸟类性别,该方法无需凝胶、快速且成本低廉。利用蛇雕(Spilornis cheela hoya,S. c. hoya)和白头鹎(Pycnonotus sinensis,P. sinensis)对这种新型分子性别鉴定技术进行了验证。S. c. hoya和P. sinensis的CHD基因长度差异分别为13bp和52bp。使用格里菲斯(Griffiths)的P2/P8引物时,S. c. hoya的PCR/电泳以及S. c. hoya和P. sinensis的PCR/MCA均无法实现分子性别鉴定。相比之下,我们重新设计了性别特异性引物,利用PCR/MCA分别获得了S. c. hoya的CHD-Z和CHD-W基因长度为185bp和112bp的PCR产物。使用该特异性引物组,至少可同时检测13个S. c. hoya样本,并区分CHD-Z和CHD-W PCR产物的熔解温度(Tm)峰。
在本研究中,我们引入了一种高通量鸟类分子性别鉴定技术,并成功应用于两个物种。这种新方法在其他鸟类物种的高通量性别鉴定中也具有巨大的应用潜力。