Overexpression of human BAG3^P209L in mice causes restrictive cardiomyopathy.

ABSTRACT: An amino acid exchange (P209L) in the HSPB8 binding site of the human co-chaperone BAG3 gives rise to severe childhood cardiomyopathy. To phenocopy the disease in mice and gain insight into its mechanisms, we generated humanized transgenic mouse models. Expression of human BAG3^P209L-eGFP in mice caused Z-disc disintegration and formation of protein aggregates. This was accompanied by massive fibrosis resulting in early-onset restrictive cardiomyopathy with increased mortality as observed in patients. RNA-Seq and proteomics revealed changes in the protein quality control system and increased autophagy in hearts from hBAG3^P209L-eGFP mice. The mutation renders hBAG3^P209L less soluble in vivo and induces protein aggregation, but does not abrogate hBAG3 binding

SUBMITTER: Kimura K 

PROVIDER: S-EPMC8196106 | biostudies-literature | 2021 Jun

REPOSITORIES: biostudies-literature