Analysis of ADAR1 gene variants in two pedigrees affected with dyschromatosis symmetrica hereditaria.
10.3760/cma.j.cn511374-20200413-00256
- Author:
Qian MA
1
;
Jinlin WU
;
Xiangdong KONG
Author Information
1. Genetics and Prenatal Diagnosis Center, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, China. kongxd@zzu.edu.cn.
- Publication Type:Journal Article
- MeSH:
Adenosine Deaminase/genetics*;
Humans;
Mutation;
Pedigree;
Pigmentation Disorders/genetics*;
RNA-Binding Proteins/genetics*
- From:
Chinese Journal of Medical Genetics
2020;37(11):1233-1235
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To detect variants of ADAR1 gene in two Chinese pedigrees affected with dyschromatosis symmetrica hereditaria (DSH).
METHODS:Clinical data and peripheral blood samples of the pedigrees were collected. All exons of the ADAR1 gene were amplified by PCR and subjected to Sanger sequencing. Suspected pathogenic variants were validated among other members of the pedigrees and 100 unrelated healthy controls.
RESULTS:For pedigree 1, Sanger sequencing has identified a heterozygous missense variant c.3002G>C (p.Asp968His) in exon 11 of the ADAR1 gene in the proband and his father. For pedigree 2, a novel nonsense variant c.3145C>T (p.Gln1049Ter) was identified in exon 12 of the ADAR1 gene in the proband and his son, which were previously unreported and absent among the healthy controls.
CONCLUSION:The c.3002G>C (p.Asp968His) and c.3145C>T (p.Gln1049Ter)variants of the ADAR1 gene probably underlay the DSH in the two pedigrees.
