RRC ID 302
著者 Kanuka H, Kuranaga E, Hiratou T, Igaki T, Nelson B, Okano H, Miura M.
タイトル Cytosol-endoplasmic reticulum interplay by Sec61alpha translocon in polyglutamine-mediated neurotoxicity in Drosophila.
ジャーナル Proc Natl Acad Sci U S A
Abstract Intracellular deposition of aggregated and ubiquitinated proteins is a prominent cytopathological feature of most neurodegenerative disorders frequently correlated with neural cell death. To elucidate mechanisms in neural cell death and degeneration, we characterized the Drosophila ortholog of Sec61alpha (DSec61alpha), a component of the translocon that is involved in both protein import and endoplasmic reticulum-associated degradation. Loss-of-function experiments for DSec61alpha revealed that the translocon contributes to expanded polyglutamine-mediated neuronal toxicity, likely resulting from proteasome inhibition and leading to accumulation of ubiquitinated proteins. Taken together, proteasome inhibition by expanded polyglutamine tracts may lead to the accumulation of toxic undegraded proteins normally transported by the Sec61alpha translocon.
巻・号 100(20)
ページ 11723-8
公開日 2003-9-30
DOI 10.1073/pnas.1934748100
PII 1934748100
PMID 14504396
PMC PMC208825
MeSH Animals Carrier Proteins / genetics* Cell Line Cysteine Endopeptidases Cytosol / metabolism* Drosophila Endoplasmic Reticulum / metabolism* Multienzyme Complexes / antagonists & inhibitors Nervous System / cytology Nervous System / drug effects* Peptides / toxicity* Proteasome Endopeptidase Complex Ubiquitin / metabolism
IF 9.412
引用数 15
WOS 分野 BIOCHEMISTRY & MOLECULAR BIOLOGY
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