OSER1 Overexpression Extends Life in Short-Lived Species
Transcription factors form one portion of the complex cell nucleus protein machinery that regulates gene expression. One transcription factor typically regulates the expression of many different genes, often largely related to one set of cellular processes. Exploring the biochemistry of transcription factor activity is one way to try to divide the complexity of the cell into different functional areas that are at least a little independent of one another. In exploring the effects of FOXO transcription factors on aging, researchers have found that upregulation of the target gene OSER1 appears to be important in slowing aging. OSER1 is, like klotho, one of the few longevity-associated genes that work in both directions: more of it means a longer life, and less of it means a shorter life.
FOXO transcription factors modulate aging-related pathways and influence longevity in multiple species, but the transcriptional targets that mediate these effects remain largely unknown. Here, we identify an evolutionarily conserved FOXO target gene, Oxidative stress-responsive serine-rich protein 1 (OSER1), whose overexpression extends lifespan in silkworms, nematodes, and flies, while its depletion correspondingly shortens lifespan.
In flies, overexpression of OSER1 increases resistance to oxidative stress, starvation, and heat shock, while OSER1-depleted flies are more vulnerable to these stressors. In silkworms, hydrogen peroxide both induces and is scavenged by OSER1 in vitro and in vivo. Knockdown of OSER1 in Caenorhabditis elegans leads to increased ROS production and shorter lifespan, mitochondrial fragmentation, decreased mitochondrial ATP production, and altered transcription of mitochondrial genes.
Human proteomic analysis suggests that OSER1 plays roles in oxidative stress response, cellular senescence, and reproduction, which is consistent with the data and suggests that OSER1 could play a role in fertility in silkworms and nematodes. Human studies demonstrate that polymorphic variants in OSER1 are associated with human longevity. In summary, OSER1 is an evolutionarily conserved FOXO-regulated protein that improves resistance to oxidative stress, maintains mitochondrial functional integrity, and increases lifespan in multiple species. Additional studies will clarify the role of OSER1 as a critical effector of healthy aging.
Anyone aware of any studies of OSER1 upregulation having a similar life extension effect in mice?