Identification and functional analysis of a novel HAND1 mutation associated with congenital ventricular septal defect
10.11817/j.issn.1672-7347.2017.12.005
- VernacularTitle:先天性室间隔缺损相关HAND1基因新突变的识别及功能
- Author:
Cheng WANG
1
;
Bin ZHOU
;
Xiangqing KONG
Author Information
1. 南京医科大学第一附属医院心内科
- Keywords:
congenital heart disease;
ventricular septal defect;
genetics;
transcriptional factor;
HAND1 gene
- From:
Journal of Central South University(Medical Sciences)
2017;42(12):1383-1388
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To identify the novel HAND 1 mutation associated with congenital ventricular septal defect (VSD) and to perform the functional analysis.Methods:A total of 125 patients with congenital VSD and 210 control individuals were recruited,and their clinical data and blood samples were collected.The genomic DNA from each study subject was isolated,and all the coding exons of HAND1 were amplified.The amplicons from HAND 1 were sequenced to identify a sequence variation.The functional characteristics of the mutant HAND 1 were analyzed by a dual-luciferase reporter assay system.Results:A novel heterozygous HAND1 mutation c.355G＞T,equivalent to E119X,was identified in a patient with sporadic VSD.This nonsense mutation was absent in the 210 control subjects.Functional analysis revealed that the mutant HAND1 lost the ability to transactivate a target gene.Conclusion:A novel HAND1 mutation with VSD is identified in this study.
