Auxin treatment increases lifespan in Caenorhabditis elegans

被引:10
|
作者
Loose, Julia A. [1 ]
Ghazi, Arjumand [1 ,2 ,3 ]
机构
[1] Univ Pittsburgh, Childrens Hosp Pittsburgh, Rangos Res Ctr, Dept Pediat,Sch Med, Pittsburgh, PA 15224 USA
[2] Univ Pittsburgh, Childrens Hosp Pittsburgh, Sch Med, Rangos Res Ctr,Dept Dev Biol, Pittsburgh, PA 15224 USA
[3] Univ Pittsburgh, Childrens Hosp Pittsburgh, Sch Med, Rangos Res Ctr,Dept Cell Biol & Physiol, Pittsburgh, PA 15224 USA
来源
BIOLOGY OPEN | 2021年 / 10卷 / 05期
基金
美国国家卫生研究院;
关键词
Caenorhabditis elegans; Aging; Auxin; Lifespan; Protein degradation; Stress; DEGRON SYSTEM; LONGEVITY; PROTEINS; TIR1; RNAI;
D O I
10.1242/bio.058703
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The auxin-inducible degradation system (AID) has proven to be a highly versatile technology for rapid, robust and reversible depletion of proteins in multiple model systems. In recent years, AID has been adapted into the nematode Caenorhabditis elegans as a tool for conditional protein knockdown. Numerous transgenic strains have been created that, upon auxin exposure, undergo protein inactivation in the wormgermline or somatic tissues, both during development and in young adults. Since longevity assays often involve long-term gene- and protein-manipulation, the facility for spatiotemporally precise and extended protein removal makes AID a potentially highly valuable tool for aging biology. However, whether auxins themselves impact worm longevity has not been directly addressed. Here, we show that prolonged exposure to indole 3-acetic acid (IAA), the auxin used in worm AID studies, extends lifespan. We also report that two transgenic strains expressing Arabidopsis proteins that are key components of the AID platform are longer lived than wild-type animals. Together, our results highlight the necessity for exercising caution while utilizing AID for longevity studies and in interpreting the resulting data. This article has an associated First Person interview with the first author of the paper.
引用
收藏
页数:7
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