Germline and mosaic variants in PRKACA and PRKACB cause a multiple congenital malformation syndrome
Details
Publication Year 2020-11-05,Volume 107,Issue #5,Page 977-988
Journal Title
American Journal of Human Genetics
Publication Type
Journal Article
Abstract
PRKACA and PRKACB code for two catalytic subunits (Cα and Cβ) of cAMP-dependent protein kinase (PKA), a pleiotropic holoenzyme that regulates numerous fundamental biological processes such as metabolism, development, memory, and immune response. We report seven unrelated individuals presenting with a multiple congenital malformation syndrome in whom we identified heterozygous germline or mosaic missense variants in PRKACA or PRKACB. Three affected individuals were found with the same PRKACA variant, and the other four had different PRKACB mutations. In most cases, the mutations arose de novo, and two individuals had offspring with the same condition. Nearly all affected individuals and their affected offspring shared an atrioventricular septal defect or a common atrium along with postaxial polydactyly. Additional features included skeletal abnormalities and ectodermal defects of variable severity in five individuals, cognitive deficit in two individuals, and various unusual tumors in one individual. We investigated the structural and functional consequences of the variants identified in PRKACA and PRKACB through the use of several computational and experimental approaches, and we found that they lead to PKA holoenzymes which are more sensitive to activation by cAMP than are the wild-type proteins. Furthermore, expression of PRKACA or PRKACB variants detected in the affected individuals inhibited hedgehog signaling in NIH 3T3 fibroblasts, thereby providing an underlying mechanism for the developmental defects observed in these cases. Our findings highlight the importance of both Cα and Cβ subunits of PKA during human development.
Publisher
Cell Press
Keywords
Ellis-van Creveld syndrome; GLI transcritpion factors; Pka; Prkaca; Prkacb; cAMP signaling; congenital heart defects; hedgehog signaling; mosaicism; postaxial polydactyly
Research Division(s)
Population Health And Immunity
PubMed ID
33058759
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 2021-02-01 12:05:20
Last Modified: 2021-03-02 10:14:37
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