Department of Ophthalmology, Yangpu District Central Hospital, Shanghai, People's Republic of China.
OMICS. 2011 Oct;15(10):665-71. doi: 10.1089/omi.2011.0034. Epub 2011 Jul 13.
Aging is characterized by the interlocking decay of biological functions over time. Microarrays have been successful in elucidating some of the genome-wide changes that occur with age. Using the AGEMAP dataset that catalogs changes in gene expression as a function of age in 16 tissues in mice, we identified tissue-specific aging genes. Coordinated aging processes across different tissues then were clarified in crosstissue coexpression networks on both the gene and pathway levels. Our findings provide more concrete information about coordinated aging across different tissues. By bridging gene-level and tissue-level research, this study could help identify targets for attenuation of critical aging-related genes, pathways, or networks for antiaging intervention.
衰老是指随着时间的推移,生物功能的连锁衰退。微阵列已经成功地阐明了一些与年龄相关的全基因组变化。使用 AGEMAP 数据集,该数据集记录了 16 种组织中基因表达随年龄变化的情况,我们鉴定了组织特异性衰老基因。然后,在基因和途径水平的跨组织共表达网络中,阐明了不同组织之间协调的衰老过程。我们的研究结果为不同组织之间的协调衰老提供了更具体的信息。通过连接基因水平和组织水平的研究,这项研究可以帮助确定衰减关键衰老相关基因、途径或网络的靶点,以进行抗衰老干预。