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Loss of function of the nuclear envelope protein LEMD2 causes DNA damage–dependent cardiomyopathy
Xurde M. Caravia, … , Ning Liu, Eric N. Olson
Xurde M. Caravia, … , Ning Liu, Eric N. Olson
Published November 15, 2022
Citation Information: J Clin Invest. 2022;132(22):e158897. https://doi.org/10.1172/JCI158897.
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Research Article Cardiology

Loss of function of the nuclear envelope protein LEMD2 causes DNA damage–dependent cardiomyopathy

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Abstract

Mutations in nuclear envelope proteins (NEPs) cause devastating genetic diseases, known as envelopathies, that primarily affect the heart and skeletal muscle. A mutation in the NEP LEM domain–containing protein 2 (LEMD2) causes severe cardiomyopathy in humans. However, the roles of LEMD2 in the heart and the pathological mechanisms responsible for its association with cardiac disease are unknown. We generated knockin (KI) mice carrying the human c.T38>G Lemd2 mutation, which causes a missense amino acid exchange (p.L13>R) in the LEM domain of the protein. These mice represent a preclinical model that phenocopies the human disease, as they developed severe dilated cardiomyopathy and cardiac fibrosis leading to premature death. At the cellular level, KI/KI cardiomyocytes exhibited disorganization of the transcriptionally silent heterochromatin associated with the nuclear envelope. Moreover, mice with cardiac-specific deletion of Lemd2 also died shortly after birth due to heart abnormalities. Cardiomyocytes lacking Lemd2 displayed nuclear envelope deformations and extensive DNA damage and apoptosis linked to p53 activation. Importantly, cardiomyocyte-specific Lemd2 gene therapy via adeno-associated virus rescued cardiac function in KI/KI mice. Together, our results reveal the essentiality of LEMD2 for genome stability and cardiac function and unveil its mechanistic association with human disease.

Authors

Xurde M. Caravia, Andres Ramirez-Martinez, Peiheng Gan, Feng Wang, John R. McAnally, Lin Xu, Rhonda Bassel-Duby, Ning Liu, Eric N. Olson

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Figure 5

Lemd2 deficiency in the heart leads to cardiomyopathy and premature death in mice.

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Lemd2 deficiency in the heart leads to cardiomyopathy and premature dea...
(A) Representative photograph of Lemd2fl/fl (left) and cKO (right) mice at P7. Scale bar: 1 cm. (B) Survival curve of Lemd2fl/fl (n = 19) and cKO (n = 23) mice. ****P < 0.0001, log-rank (Mantel-Cox) test. (C) Echocardiographic analysis of systolic EF of hearts from Lemd2fl/fl (n = 7) and cKO (n = 3) mice (from 2 to 10 postnatal days).**P < 0.01, 2-tailed, unpaired t test. (D) Echocardiographic analysis of systolic FS of hearts from Lemd2fl/fl (n = 7) and cKO (n = 3) mice (from 2 to 10 postnatal days). **P < 0.01, 2-tailed, unpaired t test. (E) H&E staining of 4-chamber view P7 hearts from Lemd2fl/fl and cKO mice. Scale bar: 500 μm. Note the atrial thrombi in cKO hearts. (F) Heatmap showing the DE genes in Lemd2fl/fl and cKO mice. n = 3 mice per genotype. Expression level in Z-score. FDR-adjusted P value of 0.05 was used as cutoff, Benjamini–Hochberg method. (G) Enriched GO terms up- and downregulated in cKO compared with Lemd2fl/fl mice. n = 3 mice per genotype. P < 0.01. (H) Upstream regulator analysis of DE genes in cKO mice compared with Lemd2fl/fl mice. n = 4 mice per genotype. Activation in Z-score.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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