PUBLICATION
WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation
- Authors
- Hao, L., Ma, J., Wu, F., Ma, X., Qian, M., Sheng, W., Yan, T., Tang, N., Jiang, X., Zhang, B., Xiao, D., Qian, Y., Zhang, J., Jiang, N., Zhou, W., Chen, W., Ma, D., Huang, G.
- ID
- ZDB-PUB-220710-15
- Date
- 2022
- Source
- Clinical and translational medicine 12: e941 (Journal)
- Registered Authors
- Keywords
- cardiomyocyte proliferation, cell cycle, congenital heart disease, spindle assembly, the WDR62 gene
- MeSH Terms
-
- Animals
- Aurora Kinase A/genetics
- Aurora Kinase A/metabolism
- Cell Cycle Proteins*/genetics
- Cell Cycle Proteins*/metabolism
- Cell Division
- Exome
- Heart Defects, Congenital*/genetics
- Heart Septal Defects, Ventricular*/genetics
- Humans
- Mice
- Myocytes, Cardiac*/cytology
- Myocytes, Cardiac*/metabolism
- Nerve Tissue Proteins/genetics
- Nerve Tissue Proteins/metabolism
- Tetralogy of Fallot*/genetics
- Zebrafish/genetics
- Zebrafish/metabolism
- PubMed
- 35808830 Full text @ Clin Transl Med
Citation
Hao, L., Ma, J., Wu, F., Ma, X., Qian, M., Sheng, W., Yan, T., Tang, N., Jiang, X., Zhang, B., Xiao, D., Qian, Y., Zhang, J., Jiang, N., Zhou, W., Chen, W., Ma, D., Huang, G. (2022) WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation. Clinical and translational medicine. 12:e941.
Abstract
Background Congenital heart disease (CHD) is the most common birth defect and has high heritability. Although some susceptibility genes have been identified, the genetic basis underlying the majority of CHD cases is still undefined.
Methods A total of 1320 unrelated CHD patients were enrolled in our study. Exome-wide association analysis between 37 tetralogy of Fallot (TOF) patients and 208 Han Chinese controls from the 1000 Genomes Project was performed to identify the novel candidate gene WD repeat-containing protein 62 (WDR62). WDR62 variants were searched in another expanded set of 200 TOF patients by Sanger sequencing. Rescue experiments in zebrafish were conducted to observe the effects of WDR62 variants. The roles of WDR62 in heart development were examined in mouse models with Wdr62 deficiency. WDR62 variants were investigated in an additional 1083 CHD patients with similar heart phenotypes to knockout mice by multiplex PCR-targeting sequencing. The cellular phenotypes of WDR62 deficiency and variants were tested in cardiomyocytes, and the molecular mechanisms were preliminarily explored by RNA-seq and co-immunoprecipitation.
Results Seven WDR62 coding variants were identified in the 237 TOF patients and all were indicated to be loss of function variants. A total of 25 coding and 22 non-coding WDR62 variants were identified in 80 (6%) of the 1320 CHD cases sequenced, with a higher proportion of WDR62 variation (8%) found in the ventricular septal defect (VSD) cohort. WDR62 deficiency resulted in a series of heart defects affecting the outflow tract and right ventricle in mouse models, including VSD as the major abnormality. Cell cycle arrest and an increased number of cells with multipolar spindles that inhibited proliferation were observed in cardiomyocytes with variants or knockdown of WDR62. WDR62 deficiency weakened the association between WDR62 and the cell cycle-regulated kinase AURKA on spindle poles, reduced the phosphorylation of AURKA, and decreased expression of target genes related to cell cycle and spindle assembly shared by WDR62 and AURKA.
Conclusions WDR62 was identified as a novel susceptibility gene for CHD with high variant frequency. WDR62 was shown to participate in the cardiac development by affecting spindle assembly and cell cycle pathway in cardiomyocytes.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping