Zhang Y, Yu W, Shen M, Fang Q, Fan M
China-Japan Friendship Institute of Clinical Medical Sciences, Beijing, P. R. China.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2000 Aug;17(4):252-5.
To study the gene mutation of Chinese patients with achondroplasia(ACH) and to set up a simple and rapid molecular diagnostic method to differentiate ACH from other similar genetic dwarfism.
The specific fragment of fibroblast growth factor receptor 3(FGFR3) transmembrane domain was amplified from dried blood spots of 21 patients with ACH and 6 suspicious patients with ACH by polymerase chain reaction, then mutation was screened and detected by restrictive enzyme analysis, single strand conformation polymorphism(SSCP) and denaturing gradient gel electrophoresis(DGGE).
One out of 6 suspicious cases was ACH and 5 were pseudoachondroplasia(PSACH). Twenty-one out of 22 patients with ACH bore a G to A transition at nucleotide 1138 and 1 bore a G to C transversion at this same position.
The nucleotide 1138 of FGFR3 gene is also the hotspot of mutation in Chinese patients with ACH. A simple and rapid molecular diagnostic method has been set up to differentiate ACH from other similar genetic dwarfism.
研究中国软骨发育不全(ACH)患者的基因突变情况,并建立一种简单快速的分子诊断方法,以将ACH与其他类似的遗传性侏儒症区分开来。
通过聚合酶链反应从21例ACH患者和6例疑似ACH患者的干血斑中扩增成纤维细胞生长因子受体3(FGFR3)跨膜结构域的特定片段,然后通过限制性酶切分析、单链构象多态性(SSCP)和变性梯度凝胶电泳(DGGE)筛选和检测突变。
6例疑似病例中有1例为ACH患者,5例为假性软骨发育不全(PSACH)。22例ACH患者中有21例在核苷酸1138处发生了G到A的转换,1例在同一位置发生了G到C的颠换。
FGFR3基因的核苷酸1138也是中国ACH患者的突变热点。已建立一种简单快速的分子诊断方法,以将ACH与其他类似的遗传性侏儒症区分开来。