Mutation analysis on DACT1 gene in children with neural tube defects in northern Chinese Han population
FANG Yu-lian
ZHAO Lin-sheng
ZHANG Rui-ping
ZHI Xiu-fang
WANG Yi-zheng
CAO Li-rong
CAI Chun-quan
Abstract:Objective To investigate the correlation between neural tube defects (NTDs) and DACT1 gene, and provide the basic data for disease diagnosis and genetic counseling. Methods Blood samples were obtained from 163 NTDs patients and 480 unrelated healthy individuals. Mutation detection of DACT1 gene and DNA direct sequencing was carried out by PCR amplification. Bioinformatics analysis of these mutated loci was performed. Results Six mutations were found in NTDs patients, including 4 missense mutations (p.R45W, p.D142G, p.N356K and p.V702G). But these mutations were not found in 480 healthy individuals. Three mutated amino acid residues (p.45R, p.142D and p.356N) were highly conservative in evolution, and the mutated carriers were female patients, and suffered from anencephaly. Conclusion DACT1 gene mutation may be a risk factor of NTDs in Han population of northern China.
Keywords:neural tube defectsmutationHan nationalityDACT1
Publication Date:2017-01-01
Online Publishing Date:2025-08-15(First online date of this platform, not the publication date of the document)
Pages:4( 297-300 )
Tianjin Medical Journal

Tianjin Medical Journal

PKUISTIC
ISSN:0253-9896
Year, Vol.(Issue):2017,45(3)