期刊
AGING-US
卷 4, 期 9, 页码 636-647出版社
IMPACT JOURNALS LLC
DOI: 10.18632/aging.100489
关键词
Werner syndrome; aging; microRNA; liver; mouse; nematode
资金
- National Institute of Health National Center for Research Resources
- Canadian Institutes of Health Research
- National Institute on Aging of the National Institutes of Health, USA
- National Health and Medical Research Council of Australia CJ Martin Early Career Fellowship (RIMS Project) [2010-01671]
Small non-coding microRNAs are believed to be involved in the mechanism of aging but nothing is known on the impact of microRNAs in the progeroid disorder Werner syndrome (WS). WS is a premature aging disorder caused by mutations in a RecQ-like DNA helicase. Mice lacking the helicase domain of the WRN ortholog exhibit many phenotypic features of WS, including a pro-oxidant status and a shorter mean life span. Caenorhabditis elegans (C. elegans) with a nonfunctional wrn-1 DNA helicase also exhibit a shorter life span. Thus, both models are relevant to study the expression of microRNAs involved in WS. In this study, we show that miR-124 expression is lost in the liver of Wrn helicase mutant mice. Interestingly, the expression of this conserved miR-124 in whole wrn-1 mutant worms is also significantly reduced. The loss of mir-124 in C. elegans increases reactive oxygen species formation and accumulation of the aging marker lipofuscin, reduces whole body ATP levels and results in a reduction in life span. Finally, supplementation of vitamin C normalizes the median life span of wrn-1 and mir-124 mutant worms. These results suggest that biological pathways involving WRN and miR-124 are conserved in the aging process across different species.
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