Inhibition of elongin C promotes longevity and protein homeostasis via HIF‐1 in C. elegans. Issue 6 (11th September 2015)

• Record Type: Journal Article
• Authors: Hwang, Wooseon; Artan, Murat; Seo, Mihwa; Lee, Dongyeop; Nam, Hong Gil; Lee, Seung‐Jae V.
• Is Part Of: Aging cell. Volume 14:Issue 6(2015:Dec.)
• Page Start: 995
• Page End: 1002
• Publication Date: 2015-09-11
• Subjects: aging -- C. elegans -- elc‐1 -- hypoxia‐inducible factor 1 -- protein homeostasis; Cells -- Aging -- Periodicals; 571.8783605
• DOI: 10.1111/acel.12390
• Languages: English
• ISSNs: 1474-9718

Abstract

Summary: The transcription factor hypoxia‐inducible factor 1 (HIF‐1) is crucial for responses to low oxygen and promotes longevity in Caenorhabditis elegans . We previously performed a genomewide RNA interference screen and identified many genes that act as potential negative regulators of HIF‐1. Here, we functionally characterized these genes and found several novel genes that affected lifespan. The worm ortholog of elongin C, elc‐1, encodes a subunit of E3 ligase and transcription elongation factor. We found that knockdown of elc‐1 prolonged lifespan and delayed paralysis caused by impaired protein homeostasis. We further showed that elc‐1 RNA interference increased lifespan and protein homeostasis by upregulating HIF‐1. The roles of elongin C and HIF‐1 are well conserved in eukaryotes. Thus, our study may provide insights into the aging regulatory pathway consisting of elongin C and HIF‐1 in complex metazoans.