Section 60
Chapter 59,184

Two novel mutations of the ADAR1 gene associated with dyschromatosis symmetrica hereditaria

Liu, Y.; Zhang, Z.; Mu, Y.; Xiong, F.; Chen, X.; Yang, H.; Yang, P.; Liu, L.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi 33(2): 173-176


ISSN/ISBN: 1003-9406
PMID: 27060309
Accession: 059183913

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To identify potential mutation of the ADAR1 gene in a Chinese family and a sporadic case affected with dyschromatosis symmetrica hereditaria(DSH). Clinical data and peripheral blood samples from the pedigree and the sporadic patient were collected. Following extraction of genomic DNA, all 15 exons and exon-intron flanking sequences of the ADAR1 gene were amplified by polymerase chain reaction and subjected to direct sequencing. A novel frame-shift mutation c.2638delG (p.Asp880ThrfsX15) from the patients of the pedigree was detected in exon 8 of the ADAR1 gene. And a novel nonsense mutation c.2867C>A (p.Ser956X) was detected in exon 10 of the ADAR1 gene from the sporadic case. Neither mutation was identified among the unaffected family members nor 100 unrelated healthy controls. The frame-shift mutation c.2638delG (p.Asp880ThrfsX15) and the nonsense mutation c.2867C>A (p.Ser956X) in the ADAR1 gene probably underlie the DSH in our patients.

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