Overexpression of human BAG3P209L 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 BAG3P209L-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 hBAG3P209L-eGFP mice. The mutation renders hBAG3P209L less soluble in vivo and induces protein aggregation, but does not abrogate hBAG3 binding properties. In conclusion, we report a mouse model mimicking the human disease. Our data suggest that the disease mechanism is due to accumulation of hBAG3P209L and mouse Bag3, causing sequestering of components of the protein quality control system and autophagy machinery leading to sarcomere disruption

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch
Anmerkungen
Nature communications. - 12 (2021) , 3575, ISSN: 2041-1723

Ereignis
Veröffentlichung
(wo)
Freiburg
(wer)
Universität
(wann)
2021
Urheber
Kimura, Kenichi
Ooms, Astrid
Graf-Riesen, Kathrin
Kuppusamy, Maithreyan
Unger, Andreas
Schuld, Julia
Daerr, Jan
Lother, Achim
Geisen, Caroline
Hein, Lutz
Takahashi, Satoru
Li, Guang
Röll, Wilhelm
Bloch, Wilhelm
Ven, Petrus Frederikus Maria van der
Linke, Wolfgang
Wu, Sean M.
Huesgen, Pitter F.
Höhfeld, Jörg
Fürst, Dieter O.
Fleischmann, Bernd K.
Hesse, Michael

DOI
10.1038/s41467-021-23858-7
URN
urn:nbn:de:bsz:25-freidok-2193218
Rechteinformation
Kein Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
14.08.2025, 10:48 MESZ

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  • 2021

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