Table 2.
Evolutionary conservation of gene expression changes during brain ageing
Gene category | Human (brain) | Rhesus macaque (brain) | Rat (brain) | Mouse (brain) | Fly (organism) | Worm (organism) |
---|---|---|---|---|---|---|
Stress response | ↑ | ↑ | ↑ | ↑ | ↑ | ↑ |
Mitochondria | ↓ | ↓ | ↓ | ↓↑ | ↓ | ↓ |
Neural plasticity/synaptic function | ↓ | ↓ | ↓ | ↓ | – | – |
Inhibitory interneuron function | ↓ | ↓ | – | – | – | – |
Ubiquitin–proteasome pathway | ↓ | ↓ | – | ↓ | – | – |
Immune/inflammatory response | ↑ | – | ↑ | ↑ | ↑ | – |
Metal ion homeostasis | ↑ | – | ↑ | – | – | – |
Myelin-related proteins | ↑ | – | ↑ | – | – | – |
Glial genes | ↑ | – | ↑ | – | – | – |
Some gene categories, such as those involved in stress responses and mitochondrial function, show conserved changes during ageing, whereas others, such as inhibitory interneuron function, exhibit primate-specific changes. An upward arrow indicates that expression increases with age; a downward arrow indicates that expression decreases with age; and a dash indicates that no change in expression with age is detected. In the ageing mouse brain, different subsets of mitochondrial genes are either age-upregulated or age-downregulated (13).