期刊
AGING-US
卷 6, 期 7, 页码 524-544出版社
IMPACT JOURNALS LLC
DOI: 10.18632/aging.100677
关键词
Skeletal muscle; aging; microRNA profiling; imprinted Dlk1-Dio3; microRNA cluster; novel microRNA
资金
- Bio & Medical Technology Development Program of the National Research Foundation (NRF) - Korean government (MSIP) [20110030133, 2013M3A9B6076413, 2012M3A9B4027954]
- KRIBB Research Initiative Program
- National Research Foundation of Korea [2012M3A9B4027954] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
Skeletal muscle degenerates progressively, losing mass (sarcopenia) over time, which leads to reduced physical ability and often results in secondary diseases such as diabetes and obesity. The regulation of gene expression by microRNAs is a key event in muscle development and disease. To understand genome-wide changes in microRNAs and mRNAs during muscle aging, we sequenced microRNAs and mRNAs from mouse gastrocnemius muscles at two different ages (6 and 24 months). Thirty-four microRNAs (15 up-regulated and 19 down-regulated) were differentially expressed with age, including the microRNAs miR-206 and -434, which were differentially expressed in aged muscle in previous studies. Interestingly, eight microRNAs in a microRNA cluster at the imprinted Dlk1-Dio3 locus on chromosome 12 were coordinately down-regulated. In addition, sixteen novel microRNAs were identified. Integrative analysis of microRNA and mRNA expression revealed that microRNAs may contribute to muscle aging through the positive regulation of transcription, metabolic processes, and kinase activity. Many of the age-related microRNAs have been implicated in human muscular diseases. We suggest that genome-wide microRNA profiling will expand our knowledge of microRNA function in the muscle aging process.
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