Gene mutations in low-density lipoprotein receptor in one Chinese padigree with homozygous familial hypercholesterolemia
- VernacularTitle:一个纯合家族性高胆固醇血症家系低密度脂蛋白受体基因突变的检测
- Author:
Junfa DING
;
Fang ZHENG
;
Xin ZHOU
;
Xiaohuan CHENG
;
Junjie MA
;
Yongmei CHEN
- Publication Type:Journal Article
- Keywords:
Hypercholesterolemia,familial;
Receptors,LDL;
Homozygote;
Mutation
- From:
Chinese Journal of Laboratory Medicine
2008;31(7):774-779
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate low density lipoprotein receptor (LDLR)gene mutation in familial hypercholesterolemia (FH) patients. Methods The proband was given clinical diagnosis of homozygous FH based on marked features and blood lipid tests results. After apoB100R3500Q mutation was excluded, the promoter region and all of the 18 exons of LDLR gene were amplified by touch-downpolymerase chain reaction (PCR). The PCR products were analyzed by single-strand conformationalpolymorphism (SSCP). The PCR products with abnormal single strands were sequenced directly. Thesecondary structures of the mutational and wild type proteins were analyzed and compared byANTHEPROT5.0, and then the tertiary structures of the mutant and wild type LDLR were predicted atSWISS MODEL homepage online. Results A homozygous mutation A606T at exon 13 of the patients wasfound by SSCP and confirmed by DNA sequencing. GOR Ⅰ method in ANTHEPROT5.0 indicates that therandom coils and turns would replace some helixes at the mutation site. The online prediction from theSWISS MODEL homepage indicates the backbone structure of the mutant LDLR has no difference from thewild type one. Conclusion The results suggest the A606T mutation of LDLR gene is the cause of the FH inthis pedigree.
