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Maintenance of sarcomeric integrity in adult muscle cells crucially depends on Z-disc anchored titin.


ABSTRACT: The giant protein titin is thought to be required for sarcomeric integrity in mature myocytes, but direct evidence for this hypothesis is limited. Here, we describe a mouse model in which Z-disc-anchored TTN is depleted in adult skeletal muscles. Inactivation of TTN causes sarcomere disassembly and Z-disc deformations, force impairment, myocyte de-stiffening, upregulation of TTN-binding mechanosensitive proteins and activation of protein quality-control pathways, concomitant with preferential loss of thick-filament proteins. Interestingly, expression of the myosin-bound Cronos-isoform of TTN, generated from an alternative promoter not affected by the targeting strategy, does not prevent deterioration of sarcomere formation and maintenance. Finally, we demonstrate that loss of Z-disc-anchored TTN recapitulates muscle remodeling in critical illness 'myosinopathy' patients, characterized by TTN-depletion and loss of thick filaments. We conclude that full-length TTN is required to integrate Z-disc and A-band proteins into the mature sarcomere, a function that is lost when TTN expression is pathologically lowered.

SUBMITTER: Swist S 

PROVIDER: S-EPMC7478974 | biostudies-literature | 2020 Sep

REPOSITORIES: biostudies-literature

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Maintenance of sarcomeric integrity in adult muscle cells crucially depends on Z-disc anchored titin.

Swist Sandra S   Unger Andreas A   Li Yong Y   Vöge Anja A   von Frieling-Salewsky Marion M   Skärlén Åsa Å   Cacciani Nicola N   Braun Thomas T   Larsson Lars L   Linke Wolfgang A WA  

Nature communications 20200908 1


The giant protein titin is thought to be required for sarcomeric integrity in mature myocytes, but direct evidence for this hypothesis is limited. Here, we describe a mouse model in which Z-disc-anchored TTN is depleted in adult skeletal muscles. Inactivation of TTN causes sarcomere disassembly and Z-disc deformations, force impairment, myocyte de-stiffening, upregulation of TTN-binding mechanosensitive proteins and activation of protein quality-control pathways, concomitant with preferential lo  ...[more]

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