Age-associated miRNA Alterations in Skeletal Muscle from Rhesus Monkeys reversed by caloric restriction

被引:87
|
作者
Mercken, Evi M. [1 ]
Majounie, Elisa [2 ]
Ding, Jinhui [2 ]
Guo, Rong [3 ]
Kim, Jiyoung [3 ]
Bernier, Michel [1 ]
Mattison, Julie [1 ]
Cookson, Mark R. [2 ]
Gorospe, Myriam [3 ]
de Cabo, Rafael [1 ]
Abdelmohsen, Kotb [3 ]
机构
[1] NIA, Expt Gerontol Sect, Translat Gerontol Branch, NIH, Baltimore, MD 21224 USA
[2] NIA, Cell Biol & Gene Express Sect, Neurogenet Lab, NIH, Bethesda, MD 20892 USA
[3] NIA, Genet Lab, NIH, Baltimore, MD 21224 USA
来源
AGING-US | 2013年 / 5卷 / 09期
基金
美国国家卫生研究院;
关键词
gene expression; posttranscriptional gene regulation; muscle aging; muscle diseases; GENE-EXPRESSION; MICRORNA EXPRESSION; TRANSCRIPTION FACTORS; IV COLLAGEN; CANCER; SENESCENCE; SARCOPENIA; IMPACT; MICE; INFLAMMATION;
D O I
10.18632/aging.100598
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The levels of microRNAs (miRNAs) are altered under different conditions such as cancer, senescence, and aging. Here, we have identified differentially expressed miRNAs in skeletal muscle from young and old rhesus monkeys using RNA sequencing. In old muscle, several miRNAs were upregulated, including miR-451, miR-144, miR-18a and miR-15a, while a few miRNAs were downregulated, including miR-181a and miR-181b. A number of novel miRNAs were also identified, particularly in old muscle. We also examined the impact of caloric restriction (CR) on miRNA abundance by reverse transcription (RT) followed by real-time, quantitative (q)PCR analysis and found that CR rescued the levels of miR-181b and chr1:205580546, and also dampened the age-induced increase in miR-451 and miR-144 levels. Our results reveal that there are changes in expression of known and novel miRNAs with skeletal muscle aging and that CR may reverse some of these changes to a younger phenotype.
引用
收藏
页码:692 / 703
页数:12
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