Department of Physics and Astronomy, University of Bologna, Bologna, 40126, Italy.
Interdepartmental Center "L. Galvani", University of Bologna, Bologna, 40126, Italy.
Sci Rep. 2017 Jul 20;7(1):6005. doi: 10.1038/s41598-017-05694-2.
Many studies investigated age-related changes in gene expression of different tissues, with scarce agreement due to the high number of affecting factors. Similarly, no consensus has been reached on which genes change expression as a function of age and not because of environment. In this study we analysed gene expression of T lymphocytes from 27 healthy monozygotic twin couples, with ages ranging over whole adult lifespan (22 to 98 years). This unique experimental design allowed us to identify genes involved in normative aging, which expression changes independently from environmental factors. We obtained a transcriptomic signature with 125 genes, from which chronological age can be estimated. This signature has been tested in two datasets of same cell type hybridized over two different platforms, showing a significantly better performance compared to random signatures. Moreover, the same signature was applied on a dataset from a different cell type (human muscle). A lower performance was obtained, indicating the possibility that the signature is T cell-specific. As a whole our results suggest that this approach can be useful to identify age-modulated genes.
许多研究调查了不同组织中与年龄相关的基因表达变化,但由于影响因素众多,结果差异很大。同样,对于哪些基因随着年龄的增长而表达变化,哪些基因不是因为环境因素而表达变化,也没有达成共识。在这项研究中,我们分析了 27 对健康同卵双胞胎的 T 淋巴细胞的基因表达情况,年龄跨度涵盖整个成年期(22 至 98 岁)。这种独特的实验设计使我们能够识别与正常衰老相关的基因,这些基因的表达变化不受环境因素的影响。我们得到了一个由 125 个基因组成的转录组特征,通过这些基因可以估计出年龄。该特征已在两个不同平台杂交的相同细胞类型的两个数据集上进行了测试,与随机特征相比,表现明显更好。此外,相同的特征被应用于来自不同细胞类型(人类肌肉)的数据集。得到的性能较低,表明该特征可能是 T 细胞特异性的。总的来说,我们的结果表明,这种方法可用于识别受年龄调节的基因。