Hong Ping, Zhu Pei-yuan, Huang Yu-feng, Luan Jian-feng
Department of Micobiology & Immunology, Nanjing Medical University, Jiangsu, China.
Zhonghua Nan Ke Xue. 2006 Apr;12(4):333-6.
To develop a nested polymerase chain reaction (PCR) technique for fetal SRY gene identification using cell-free fetal DNA in maternal plasma.
Peripheral blood samples were obtained from 30 pregnant women and cell-free DNA was extracted by the phenol/chloroform method from plasma. The nested PCR was carried out to amplify the fragment of SRY gene by two sets of PCR primer pairs. Direct sequencing analysis was then performed on the PCR product.
Among the 17 women bearing male fetuses, SRY sequences were detected in 15 plasma samples after nested PCR amplification, while none of the 13 women bearing female fetuses had the positive results. The accuracy and sensitivity were 93.3% (28/30) and 88.2% (15/17), respectively.
The phenol/chloroform extraction for fetal DNA in maternal plasma was effective and simple. And the nested PCR amplification of SRY sequence is a convenient and low-cost approach for the non-invasive early prenatal diagnosis of sex-linked inheritant diseases.
开发一种利用孕妇血浆中游离胎儿DNA鉴定胎儿SRY基因的巢式聚合酶链反应(PCR)技术。
采集30名孕妇的外周血样本,采用酚/氯仿法从血浆中提取游离DNA。通过两组PCR引物对进行巢式PCR扩增SRY基因片段,然后对PCR产物进行直接测序分析。
在17名怀有男胎的孕妇中,巢式PCR扩增后15份血浆样本检测到SRY序列,而13名怀有女胎的孕妇均无阳性结果。准确率和灵敏度分别为93.3%(28/30)和88.2%(15/17)。
酚/氯仿法提取孕妇血浆中胎儿DNA有效且简便。SRY序列的巢式PCR扩增是一种用于性连锁遗传病非侵入性早期产前诊断的便捷、低成本方法。