Inhibition of elongin C promotes longevity and protein homeostasis via HIF-1 in C. elegans.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 26361075.
- Also identified by DOI 10.1111/acel.12390 and PMC identifier 4693473.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
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.
Medical subject headings
- Caenorhabditis elegans
- Caenorhabditis elegans Proteins
- Longevity
- Transcription Factors
- Ubiquitin-Protein Ligases