[Association of ventricular septal defect with rare variations of the HAND2 gene]. / 室é´é缺æä¸HAND2åºå ç½è§åå¼çå
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Zhongguo Dang Dai Er Ke Za Zhi
; 25(4): 388-393, 2023 Apr 15.
Article
in Zh
| MEDLINE
| ID: mdl-37073844
ABSTRACT
OBJECTIVES:
To study the association of ventricular septal defect (VSD) with rare variations in the promoter region of HAND2 gene, as well as related molecular mechanisms.METHODS:
Blood samples were collected from 349 children with VSD and 345 healthy controls. The target fragments were amplified by polymerase chain reaction and sequenced to identify the rare variation sites in the promoter region of the HAND2 gene. Dual-luciferase reporter assay was used to perform a functional analysis of the variation sites. Electrophoretic mobility shift assay (EMSA) was used to investigate related molecular mechanisms. TRANSFAC and JASPAR databases were used to predict transcription factors.RESULTS:
Sequencing revealed that three variation sites (g.173530852A>G, g.173531173A>G, and g.173531213C>G) were only observed in the promoter region of the HAND2 gene in 10 children with VSD, among whom 4 children had only one variation site. The dual-luciferase reporter assay revealed that g.173531213C>G reduced the transcriptional activity of the HAND2 gene promoter. EMSA and transcription factor prediction revealed that g.173531213C>G created a binding site for transcription factor.CONCLUSIONS:
The rare variation, g.173531213C>G, in the promoter region of the HAND2 gene participates in the development and progression of VSD possibly by affecting the binding of transcription factors.Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Heart Septal Defects, Ventricular
Type of study:
Prognostic_studies
/
Risk_factors_studies
Limits:
Child
/
Humans
Language:
Zh
Journal:
Zhongguo Dang Dai Er Ke Za Zhi
Year:
2023
Document type:
Article
Affiliation country:
China