Proteasomal Regulation of the Hypoxic Response Modulates Aging in C. elegans
Author(s) -
Ranjana Mehta,
Katherine A. Steinkraus,
George L. Sutphin,
Fresnida J. Ramos,
Lara S. Shamieh,
Alexander Huh,
Christina Davis,
Devon ChandlerBrown,
Matt Kaeberlein
Publication year - 2009
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.1173507
Subject(s) - proteotoxicity , ubiquitin ligase , biology , longevity , caenorhabditis elegans , ubiquitin , microbiology and biotechnology , suppressor , proteasome , insulin receptor , protein aggregation , insulin , insulin resistance , endocrinology , genetics , cancer , gene
The Caenorhabditis elegans von Hippel-Lindau tumor suppressor homolog VHL-1 is a cullin E3 ubiquitin ligase that negatively regulates the hypoxic response by promoting ubiquitination and degradation of the hypoxic response transcription factor HIF-1. Here, we report that loss of VHL-1 significantly increased life span and enhanced resistance to polyglutamine and beta-amyloid toxicity. Deletion of HIF-1 was epistatic to VHL-1, indicating that HIF-1 acts downstream of VHL-1 to modulate aging and proteotoxicity. VHL-1 and HIF-1 control longevity by a mechanism distinct from both dietary restriction and insulin-like signaling. These findings define VHL-1 and the hypoxic response as an alternative longevity and protein homeostasis pathway.
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