Mutational analysis of patients with 6-pyruvoyltetrahydrobiopterin synthesis deficiency.
- VernacularTitle:55例6-丙酮酰四氢蝶呤合成酶缺乏症基因突变分析
- Author:
Mei-qing GU
1
;
Jun YE
;
Wen-juan QIU
;
Lian-shu HAN
;
Ya-feng ZHANG
;
Xue-fan GU
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Asian Continental Ancestry Group; genetics; Base Sequence; China; DNA Mutational Analysis; Female; Genotype; Humans; Male; Metabolic Diseases; genetics; Mutation; Pedigree; Phenylalanine Hydroxylase; genetics; metabolism; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Pregnancy; Pterins; metabolism; Steroid 21-Hydroxylase; genetics; metabolism
- From: Chinese Journal of Medical Genetics 2009;26(2):183-186
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo determine the gene mutation spectrum of patients with 6-pyruvoyltetrahydrobiopterin synthesis deficiency (PTPSD) in Mainland China.
METHODSThe 6-pyruvoyltetrahydrobiopterin synthesis gene lz(PTS)lz was analyzed in 55 PTPSD patients by using PCR-restriction fragment length polymorphism (PCR-RFLP) and direct DNA sequencing. The relationship between the genotype and phenotype was analyzed.
RESULTSEighteen mutations were identified and the detection rate of gene mutation was 95.28%. Four hot-spot mutations, namely P87S (40.57%), N52S(13.21%), D96N(12.26%) and IVS1nt-291A to G(10.38%) were found in this study, and the first three were associated with severe phenotype. The P87L was reported firstly in Chinese patients, and the Q13X, M80T, IVS4nt-2A to G, L93M and K131N were novel mutations.
CONCLUSIONThe P87S, N52S, D96N and IVS1nt-291A to G mutations are the hot-spots mutations of the PTS gene in Chinese PTPSD patients. Using PCR-RFLP technique to screen the mutations in the PTS gene can increase the efficiency of gene diagnosis.
