Genetic trade-off between youth and longevity uncovered
A new study identifies vgll3 as a key gene that promotes rapid growth and early reproduction while increasing the risk of aging and cancer later in life. The findings provide rare experimental evidence for the theory that ...
Researchers say the discovery could open new paths for understanding, and potentially separating, the biological links between development, aging, and disease. The work has been published in Nature Communications.
Gene discovery and evolutionary trade-offs
Researchers have identified a gene that directly links early-life growth and reproductive success with accelerated aging and increased cancer risk later in life, offering new insight into a longstanding theory in evolutionary biology.
Now, an international team led by Dr. Eitan Moses, Dr. Marva Bergman, and Prof. Itamar Harel at Hebrew University, in collaboration with Prof. Nabieh Ayoub (Technion) and Prof. Alexei A. Maklakov (University of East Anglia), provides experimental evidence for the theory of antagonistic pleiotropy, the idea that certain genes can provide advantages early in life while contributing to disease and decline in old age.
While widely accepted in theory, scientists have struggled to identify specific genes responsible for such trade-offs in vertebrates. Using the African turquoise killifish, a short-lived species recently pioneered by Harel and colleagues for genetic aging research, the team focused on the gene vgll3, which has been previously linked to the timing of human puberty and maturation in other species, particularly Atlantic salmon.
The killifish is an emerging model for investigating the genetic architecture of aging and age-related pathologies, which often exhibit sex-specific patterns between females (left) and males (right). Credit: Itamar Harel