Mutations in exon 7 of the PAH gene in Chinese phenylketonuria patients in Xinjiang
- VernacularTitle:新疆地区苯丙氨酸羟化酶基因外显子7的突变研究
- Author:
Wu-Zhong YU
;
Dong-Hui QIU
;
Fang SONG
;
Li LIU
;
Yu-Wei JIN
;
Jiang HE
;
Jun-Hao GUI
;
Rui WANG
;
Hong-Yun ZOU
;
Zheng WANG
;
Yu ZHOU
;
Quan LEI
;
Zhanping ZHANG
;
Xingwen LIU
;
- Publication Type:Journal Article
- Keywords:
Phenylketonuria;
Phenylalanine hydroxylase;
Gene mutation;
Exon
- From:
Chinese Journal of Laboratory Medicine
2000;0(06):-
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the mutation characteristics in exon 7 of the PAH gene in phenylketonuria(PKU) patients in Xinjiang.Methods The mutations in exon 7 of PAH gene were detected by PCR/SSCP in 37 PKU patients.Results Five missense mutations including R243Q,L255S,E280G, E280K and P281L were identified in 74 chromosomes from 37 PKU patients,with relative frequencies of 18.9%,4.1%,1.4%,1.4% and 1.4% respectively.The frequency of mutant alleles in exon 7 was 27%. Among the five mutations,it was the second time the E280G mutation was reported in the world.In China,it was the second time the L255S,E280K and P281 L mutations were found.P281L and R243Q mutations were first found in 2 of Chinese Uygur.Considering the previous reports and the present study,R243Q was the most prevalent form in Asian PKU populations.P281L and E280K were two common mutations in PKU patients from European countries.However,E280G and L255S were two characteristic forms in Chinese. Condusions Characteristics of PAH gene mutations are shown in Chinese PKU population from Xinjiang, which is a special distribution belt that located between China and Europe.The results give a clue that Xinjiang could probably be an ideal genetic resource repertoire for studying diversity of gene mutations, heterogeneity of PAH gene,human genesis and migration.
