苯丙氨酸羟化酶
遗传学
基因
突变
外显子
等位基因
生物
基因突变
单链构象多态性
人口
等位基因频率
遗传多样性
氨基酸
苯丙氨酸
医学
环境卫生
作者
Wu-zhong Yu,Dong-hui Qiu,Fang Song,Li Liu,Shaoming Liu,Xin‐Jian He,Yu-wei Jin,Yanling Zhang,Hong-yun Zou,He Jiang,Lei Quan,Xing-wen Liu
出处
期刊:PubMed
日期:2009-02-01
卷期号:26 (1): 26-30
被引量:1
标识
DOI:10.3760/cma.j.issn.1003-9406.2009.01.006
摘要
To study the characteristics of the PAH gene mutation in patients with phenylketonuria (PKU) in Xinjiang area.The mutations in exons 3, 5, 6, 7, 11 and 12 and the flanking intronic sequence of the PAH gene were detected by PCR/SSCP analysis and direct DNA sequencing in 46 PKU patients.Twenty different mutations were found in 68/92 alleles (73.9%). The prevalent mutations of R243Q, EX6 96A>G, R111X, Y356X and V399V were similar to that of Northern China populations. The mutations F161S, L255S, P281L, and R413P were significantly different from that in other Chinese populations. It was the second time that E280G and A434D mutations were reported in the world, that L255S, P281L, R261Q, and I65T mutations were found in China. Thirteen different mutations were first found in Chinese Uygur, which showed a distinct ethnic characteristics.The study showed not only a distinct and conservative, but also a crossed and syncretic genetic characteristics in Xinjiang Uygur population. The results suggest that Xinjiang could be an ideal genetic resource repertoire for studying diversity of gene mutations, heterogeneity of PAH gene, human origins and migration.
科研通智能强力驱动
Strongly Powered by AbleSci AI