A novel point mutation in parkin gene was identified in an early-onset case of Parkinson's disease.
- Author:
Tao WANG
1
;
Zhihou LIANG
;
Shenggang SUN
;
Xuebing CAO
;
Hai PENG
;
Fei CAO
;
Hongjin LIU
;
Etang TONG
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Age of Onset; Aged; Base Sequence; China; DNA; chemistry; genetics; DNA Mutational Analysis; Female; Humans; Ligases; genetics; Male; Middle Aged; Mutation, Missense; Parkinson Disease; genetics; Point Mutation; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Ubiquitin-Protein Ligases
- From: Chinese Journal of Medical Genetics 2003;20(2):111-113
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the distribution of possible novel mutation of parkin gene in variant subset patients with Parkinson's disease (PD) in China and to explore the role of parkin gene in the pathogenesis of PD.
METHODSSeventy patients were divided into early onset and late-onset groups, and 70 healthy subjects were included as controls. Genomic DNA from 70 normal controls and from those of PD patients were extracted from peripheral blood leukocytes with standard procedures. Mutations of parkin gene (exons 1-12) in all subjects mentioned above were screened by PCR-SSCP. And in the samples with abnormal SSCP result, further sequencing was performed to confirm the mutation and its location.
RESULTSA new missense mutation (Gly284Arg) on exon 7 was found in a sample, while 4 samples from all subjects exhibited abnormal mobility shift on SSCP electrophoresis. All mentioned DNA variants were sourced from the samples of the patients with early-onset PD.
CONCLUSIONPoint mutation in parkin gene also contributes partly to the development of early-onset Parkinson's disease in Chinese population.
