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Identification of novel rare copy number variants associated with sporadic tetralogy of Fallot and clinical implications.
He, Guo-Wei; Maslen, Cheryl L; Chen, Huan-Xin; Hou, Hai-Tao; Bai, Xiao-Yan; Wang, Xiu-Li; Liu, Xiao-Cheng; Lu, Wan-Li; Chen, Xin-Xin; Chen, Wei-Dan; Xing, Quan-Sheng; Wu, Qin; Wang, Jun; Yang, Qin.
Afiliación
  • He GW; Institute of Cardiovascular Diseases & Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Tianjin University & Chinese Academy of Medical Sciences, Tianjin, China.
  • Maslen CL; Department of Surgery, Oregon Health and Science University, Portland, Oregon, USA.
  • Chen HX; Knight Cardiovascular Institute, Oregon Health & Science University, Portland, Oregon, USA.
  • Hou HT; Institute of Cardiovascular Diseases & Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Tianjin University & Chinese Academy of Medical Sciences, Tianjin, China.
  • Bai XY; Institute of Cardiovascular Diseases & Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Tianjin University & Chinese Academy of Medical Sciences, Tianjin, China.
  • Wang XL; Institute of Cardiovascular Diseases & Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Tianjin University & Chinese Academy of Medical Sciences, Tianjin, China.
  • Liu XC; Institute of Cardiovascular Diseases & Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Tianjin University & Chinese Academy of Medical Sciences, Tianjin, China.
  • Lu WL; Institute of Cardiovascular Diseases & Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Tianjin University & Chinese Academy of Medical Sciences, Tianjin, China.
  • Chen XX; Institute of Cardiovascular Diseases & Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Tianjin University & Chinese Academy of Medical Sciences, Tianjin, China.
  • Chen WD; Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
  • Xing QS; Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
  • Wu Q; Qingdao Women and Children's Hospital, Qingdao University, Qingdao, China.
  • Wang J; Qingdao Women and Children's Hospital, Qingdao University, Qingdao, China.
  • Yang Q; Institute of Cardiovascular Diseases & Department of Cardiovascular Surgery, TEDA International Cardiovascular Hospital, Tianjin University & Chinese Academy of Medical Sciences, Tianjin, China.
Clin Genet ; 102(5): 391-403, 2022 11.
Article en En | MEDLINE | ID: mdl-35882632
Tetralogy of Fallot (TOF) is the most common cyanotic congenital heart disease. Highly penetrant copy number variants (CNVs) and genes related to the etiology of TOF likely exist with differences among populations. We aimed to identify CNV contributions to sporadic TOF cases in Han Chinese. Genomic DNA was extracted from peripheral blood in 605 subjects (303 sporadic TOF and 302 unaffected Han Chinese [Control] from cardiac centers in China) and analyzed by genome-wide association study (GWAS). The GWAS results were compared with existing Database of Genetic Variants. These CNVs were further validated by qPCR. Bioinformatics analyses were performed with protein-protein interaction (PPI) network and KEGG pathway enrichment. Across all chromosomes 119 novel "TOF-specific CNVs" were identified with prevalence of CNVs of 21.5% in chromosomes 1-20 and 37.0% including Chr21/22. In chromosomes 1-20, CNVs on 11q25 (encompasses genes ACAD8, B3GAT1, GLB1L2, GLB1L3, IGSF9B, JAM3, LOC100128239, LOC283177, MIR4697, MIR4697HG, NCAPD3, OPCML, SPATA19, THYN1, and VPS26B) and 14q32.33 (encompasses genes THYN1, OPCML, and NCAPD3) encompass genes most likely to be associated with TOF. Specific CNVs found on the chromosome 21 (6.3%) and 22(11.9%) were also identified in details. PPI network analysis identified the genes covering the specific CNVs related to TOF and the signaling pathways. This study for first time identified novel TOF-specific CNVs in the Han Chinese with higher frequency than in Caucasians and with 11q25 and 14q32.33 not reported in TOF of Caucasians. These novel CNVs identify new candidate genes for TOF and provide new insights into genetic basis of TOF.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tetralogía de Fallot / Variaciones en el Número de Copia de ADN Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Clin Genet Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Dinamarca
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Tetralogía de Fallot / Variaciones en el Número de Copia de ADN Tipo de estudio: Diagnostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Clin Genet Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Dinamarca