Epistatic interaction of PDE4DIP and DES mutations in familial atrial fibrillation with slow conduction

Autor: Maen D. Abou Ziki, Johny Michel Abboud, Neha Bhat, Arpita Neogi, Arya Mani, Nelson Ugwu, Ya Liu, Tristan P. Driscoll, Emily Smith, Martin A. Schwartz, Joseph G. Akar, Salah Chouairi
Rok vydání: 2021
Předmět:
Zdroj: Hum Mutat
ISSN: 1098-1004
1059-7794
DOI: 10.1002/humu.24265
Popis: The genetic causes of atrial fibrillation (AF) with slow conduction are unknown. Eight kindreds with familial AF and slow conduction, including a family affected by early onset AF, heart block and incompletely penetrant non-ischemic dilated cardiomyopathy (DCM) underwent whole exome sequencing. A known pathogenic mutation in the desmin (DES) gene resulting in p.S13F substitution (NM_001927.3:c.38C>T) at a PKC phosphorylation site was identified in all four members of the kindred with early-onset AF and heart block, while only two developed DCM. Higher penetrance for AF and heart block prompted a genetic screening for DES modifier(s). A deleterious mutation in the phosphodiesterase-4D-interacting-protein (PDE4DIP) gene resulting in p.A123T substitution (NM_001002811:c.367G>A) was identified that segregated with early onset AF, heart block and the DES mutation. Three additional novel deleterious PDE4DIP mutations were identified in four other unrelated kindreds. Characterization of PDE4DIP(A123T) in vitro suggested impaired compartmentalization of PKA and PDE4D characterized by reduced colocalization with PDE4D, increased cAMP activation leading to higher PKA phosphorylation of the β2-adrenergic-receptor, and decreased PKA phosphorylation of desmin after isoproterenol stimulation. Our findings identify PDE4DIP as a novel gene for slow AF and unravel its epistatic interaction with DES mutations in development of conduction disease and arrhythmia.
Databáze: OpenAIRE
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