A microRNA switch controls dietary restriction-induced longevity through Wnt signaling

被引:19
|
作者
Xu, Yunpeng [1 ]
He, Zhidong [1 ]
Song, Mengjiao [1 ]
Zhou, Yifei [1 ]
Shen, Yidong [1 ]
机构
[1] Univ Chinese Acad Sci, CAS Ctr Excellence Mol Cell Sci, Shanghai Inst Biochem & Cell Biol,Chinese Acad Sc, Innovat Ctr Cell Signaling Network,State Key Lab, Shanghai, Peoples R China
关键词
dietary restriction; longevity; microRNA; Wnt signaling; CAENORHABDITIS-ELEGANS; CALORIC RESTRICTION; LIFE-SPAN; GENE-EXPRESSION; BETA-CATENIN; PATHWAY; AUTOPHAGY; PHA-4/FOXA; METABOLISM; BINDING;
D O I
10.15252/embr.201846888
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dietary restriction (DR) is known to have a potent and conserved longevity effect, yet its underlying molecular mechanisms remain elusive. DR modulates signaling pathways in response to nutrient status, a process that also regulates animal development. Here, we show that the suppression of Wnt signaling, a key pathway controlling development, is required for DR-induced longevity in Caenorhabditis elegans. We find that DR induces the expression of mir-235, which inhibits cwn-1/WNT4 expression by binding to the 3-UTR. The switch-on of mir-235 by DR occurs at the onset of adulthood, thereby minimizing potential disruptions in development. Our results therefore implicate that DR controls the adult lifespan by using a temporal microRNA switch to modulate Wnt signaling.
引用
收藏
页数:14
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