Analyses of coding sequence point mutation and polymorphism of TGFBI gene in Chinese patients with keratoconus.
- VernacularTitle:中国人圆锥角膜患者的TGFBI基因编码区点突变及多态性的检测和分析
- Author:
Tao GUAN
1
;
Zhang-wei MA
;
Shi-ping DING
Author Information
- Publication Type:Journal Article
- MeSH: Adolescent; Adult; Case-Control Studies; Child; China; Extracellular Matrix Proteins; genetics; Female; Glycine; deficiency; genetics; Humans; Keratoconus; genetics; Male; Middle Aged; Point Mutation; Polymerase Chain Reaction; methods; Polymorphism, Single Nucleotide; Polymorphism, Single-Stranded Conformational; Sequence Analysis, DNA; methods; Transforming Growth Factor beta; genetics; Young Adult
- From: Chinese Journal of Medical Genetics 2011;28(2):152-155
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the point mutations and polymorphisms of transforming growth factor beta-induced gene (TGFBI) in Chinese patients with keratoconus and discuss the relationship between the feature of gene mutations and single nucleotide polymorphisms of TGFBI gene and keratoconus.
METHODSPolymerase chain reaction single strand conformation polymorphism and DNA direct sequencing were performed in 30 keratoconus cases and 30 healthy controls. All 17 exons of the TGFBI gene were analyzed for point mutations and single nucleotide polymorphisms.
RESULTSTotally two heterozygous nucleotide changes were identified in exon 12 of the TGFBI gene. The codon 535 is changed from GGA to TGA in 1 patient, leading to a substitution of glycine to a stop codon at the protein level (G535X). The codon 540 is changed from TTT to TTC in 2 patients and 1 control individual, resulting in a nonsense mutation (F54F), and is a single nucleotide polymorphism of the gene.
CONCLUSIONMutation and polymorphisms of the TGFBI gene were detected in Chinese patients with keratoconus in this study. The results suggest that TGFBI gene might play an important role in the pathogenesis of keratoconus.
