How nuclear envelope dynamics can direct laminopathy phenotypes

van Heerden, David; Klima, Stefanie; van den Bout, Iman

doi:10.1016/j.ceb.2023.102290

Cited by 1 publication

(1 citation statement)

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“…Mutations in genes encoding nesprins and other members of the LINC complex are associated with several human pathologies ( De Silva et al, 2023 ; Horn, 2014 ; Storey and Fuller, 2022 ; van Heerden et al, 2023 ). Mutations in the nesprin SYNE1 are most often found in spinocerebellar ataxia 8 (SCAR8) with these mutations distributed throughout the protein including the spectrin repeat region(s) and the CH domain, as well as the KASH domain ( Storey and Fuller, 2022 ).…”

Section: Discussionmentioning

confidence: 99%

The Drosophila Nesprin-1 homolog MSP300 is required for muscle autophagy and proteostasis

van der Graaf,

Srivastav,

Nishad

et al. 2024

Journal of Cell Science

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Nesprin proteins, which are components of the LINC complex, are located within the nuclear envelope and play prominent roles in nuclear architecture. For example, LINC complex proteins interact with both chromatin and the cytoskeleton. Here we report that the Drosophila Nesprin MSP300 has an additional function in autophagy within larval body wall muscles. RNAi-mediated MSP300 knockdown in larval body wall muscles resulted in defects in the contractile apparatus, muscle degeneration, and defective autophagy. In particular, MSP300 knockdown caused accumulation of cytoplasmic aggregates that contained poly-ubiquitinated cargo, as well as the autophagy receptor ref(2)P/p62/SQSTM and Atg8a. Furthermore, MSP300 knockdown larvae expressing an mCh-GFP-tagged Atg8a transgene exhibited aberrant persistence of the GFP signal within these aggregates, indicating failure of autophagosome maturation. These autophagy deficits were similar to those exhibited by loss of the ER fusion protein Atlastin (Atl), raising the possibility that Atl and MSP300 might function in the same pathway. In support of this possibility, we found that a GFP-tagged MSP300 protein trap exhibit extensive localization to the ER. Alteration of ER-directed MSP300 might abrogate important cytoskeletal contacts necessary for autophagosome completion.

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