| Literature DB >> 31533046 |
Tea Shavlakadze1, Melody Morris2, Jian Fang3, Sharon X Wang3, Jiang Zhu4, Weihua Zhou3, Herman W Tse3, Ricardo Mondragon-Gonzalez3, Guglielmo Roma5, David J Glass6.
Abstract
To understand the changes in gene expression that occur as a result of age, which might create a permissive or causal environment for age-related diseases, we produce a multi-time point age-related gene expression signature (AGES) from liver, kidney, skeletal muscle, and hippocampus of rats, comparing 6-, 9-, 12-, 18-, 21-, 24-, and 27-month-old animals. We focus on genes that changed in one direction throughout the lifespan of the animal, either early in life (early logistic changes), at mid-age (mid-logistic), late in life (late-logistic), or linearly, throughout the lifespan of the animal. The pathways perturbed because of chronological age demonstrate organ-specific and more-global effects of aging and point to mechanisms that could potentially be counter-regulated pharmacologically to treat age-associated diseases. A small number of genes are regulated by aging in the same manner in every tissue, suggesting they may be more-universal markers of aging.Entities:
Keywords: RNA-seq; ageing; aging; aging gene signature; gene expression; hippocampus; inflammation; kidney; liver; mitochondria; muscle; rat
Year: 2019 PMID: 31533046 DOI: 10.1016/j.celrep.2019.08.043
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423