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Proteotoxic stresses stimulate dissociation of UBL4A from the tail-anchored protein recognition complex.

ABSTRACT: Inclusion body formation is associated with cytotoxicity in a number of neurodegenerative diseases. However, the molecular basis of the toxicity caused by the accumulation of aggregation-prone proteins remains controversial. In this study, we found that disease-associated inclusions induced by elongated polyglutamine chains disrupt the complex formation of BAG6 with UBL4A, a mammalian homologue of yeast Get5. UBL4A also dissociated from BAG6 in response to proteotoxic stresses such as proteasomal inhibition and mitochondrial depolarization. These findings imply that the cytotoxicity of pathological protein aggregates might be attributed in part to disruption of the BAG6-UBL4A complex that is required for the biogenesis of tail-anchored proteins.

SUBMITTER: Hagiwara T

PROVIDER: S-EPMC10586765 | biostudies-literature | 2023 Oct

REPOSITORIES: biostudies-literature

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Proteotoxic stresses stimulate dissociation of UBL4A from the tail-anchored protein recognition complex.

Hagiwara Takumi T Minami Ryosuke R Ushio Chizuru C Yokota Naoto N Kawahara Hiroyuki H

The Biochemical journal 20231001 19

Inclusion body formation is associated with cytotoxicity in a number of neurodegenerative diseases. However, the molecular basis of the toxicity caused by the accumulation of aggregation-prone proteins remains controversial. In this study, we found that disease-associated inclusions induced by elongated polyglutamine chains disrupt the complex formation of BAG6 with UBL4A, a mammalian homologue of yeast Get5. UBL4A also dissociated from BAG6 in response to proteotoxic stresses such as proteasoma ...[more]

PMID: 37747814

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