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A secreted microRNA disrupts autophagy in distinct tissues of Caenorhabditis elegans upon ageing.


ABSTRACT: Macroautophagy, a key player in protein quality control, is proposed to be systematically impaired in distinct tissues and causes coordinated disruption of protein homeostasis and ageing throughout the body. Although tissue-specific changes in autophagy and ageing have been extensively explored, the mechanism underlying the inter-tissue regulation of autophagy with ageing is poorly understood. Here, we show that a secreted microRNA, mir-83/miR-29, controls the age-related decrease in macroautophagy across tissues in Caenorhabditis elegans. Upregulated in the intestine by hsf-1/HSF1 with age, mir-83 is transported across tissues potentially via extracellular vesicles and disrupts macroautophagy by suppressing CUP-5/MCOLN, a vital autophagy regulator, autonomously in the intestine as well as non-autonomously in body wall muscle. Mutating mir-83 thereby enhances macroautophagy in different tissues, promoting protein homeostasis and longevity. These findings thus identify a microRNA-based mechanism to coordinate the decreasing macroautophagy in various tissues with age.

SUBMITTER: Zhou Y 

PROVIDER: S-EPMC6811558 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature

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A secreted microRNA disrupts autophagy in distinct tissues of Caenorhabditis elegans upon ageing.

Zhou Yifei Y   Wang Xueqing X   Song Mengjiao M   He Zhidong Z   Cui Guizhong G   Peng Guangdun G   Dieterich Christoph C   Antebi Adam A   Jing Naihe N   Shen Yidong Y  

Nature communications 20191023 1


Macroautophagy, a key player in protein quality control, is proposed to be systematically impaired in distinct tissues and causes coordinated disruption of protein homeostasis and ageing throughout the body. Although tissue-specific changes in autophagy and ageing have been extensively explored, the mechanism underlying the inter-tissue regulation of autophagy with ageing is poorly understood. Here, we show that a secreted microRNA, mir-83/miR-29, controls the age-related decrease in macroautoph  ...[more]

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