The establishment of a high resolution melting analysis based rapid screening system for UGT1A1 gene mutation
10.3760/cma.j.issn.1009-9158.2017.02.006
- VernacularTitle:高分辨熔解曲线技术快速筛查 UGT1 A1基因变异
- Author:
Hui YANG
;
Liye YANG
;
Lei ZHENG
;
Zhen CAI
- Keywords:
Gilbert disease;
Crigler-Najjar syndrome;
Hyperbilirubinemia,neonatal;
Glucuronosyltransferase;
Mutation;
Polymerase chain reaction;
High resolution melting
- From:
Chinese Journal of Laboratory Medicine
2017;40(2):101-104
- CountryChina
- Language:Chinese
-
Abstract:
Objective To develop a high-resolution melting ( HRM ) assay for rapidly screening Gilbert syndrome ( GS) and Crigler-Najjar syndrome ( CNS) associated with UGT1A1 defects.Method Methodology was developed .Then, we applied the established method to analyze 61 clinical samples from neonatal patients with severe unexplained unconjugated hyperbilirubinemia .Neonates with known risk factors for developing hyperbilirubinemia , such as ABO hemolysis, G6PD deficiency, sepsis, hypoxic ischemic encephalopathy were excluded .Five pairs of PCR primers were designed to detect the five common mutations (G211A, C686A, C1091T, C1352T and T1456G) in Asia population.PCR and HRM Assay conditions were optimized.UGT1A1 genotyping in clinical samples was performed by using the established HRM analysis , and all results were subsequently confirmed by direct DNA sequencing .Results The mutants were readily differentiated by using HRM analysis .In this study, 42 neonates were identified with UGT1A1 mutation, and 4 different known variants were detected .Conclusion HRM analysis in this study was economical, convenient, rapid, effective for screening UGT1A1 gene mutations, which can serve as an reliable method for the clinical diagnosis of GS and CNS and the large-scale molecular epidemiological research of UGT1A1 gene-related diseases.
