Supported by a grant from the Ellison Medical Foundation, the Glenn Foundation for Medical Research, the A-T Children's Project, and the NIA/NIH.
The search for evolutionary developmental origins of aging in zebrafish: A novel intersection of developmental and senescence biology in the zebrafish model system†
Article first published online: 19 SEP 2011
Copyright © 2011 Wiley-Liss, Inc.
Birth Defects Research Part C: Embryo Today: Reviews
Special Issue: Zebrafish Development: Basic Science to Translational Research (2)
Volume 93, Issue 3, pages 229–248, September 2011
How to Cite
Kishi, S. (2011), The search for evolutionary developmental origins of aging in zebrafish: A novel intersection of developmental and senescence biology in the zebrafish model system. Birth Defects Research Part C: Embryo Today: Reviews, 93: 229–248. doi: 10.1002/bdrc.20217
- Issue published online: 19 SEP 2011
- Article first published online: 19 SEP 2011
- Ellison Medical Foundation
- Glenn Foundation for Medical Research
- A-T Children's Project
Senescence may be considered the antithesis of early development, but yet there may be factors and mechanisms in common between these two phenomena during the process of aging. We investigated whether any relationship exists between the regulatory mechanisms that function in early development and in senescence using the zebrafish (Danio rerio), a small freshwater fish and a useful model animal for genetic studies. We conducted experiments to isolate zebrafish mutants expressing an apparent senescence phenotype during embryogenesis (embryonic senescence). Some of the genes we thereby identified had already been associated with cellular senescence and chronological aging in other organisms, but many had not yet been linked to these processes. Complete loss-of-function of developmentally essential genes induce embryonic (or larval) lethality, whereas it seems like their partial loss-of-function (i.e., decrease-of-function by heterozygote or hypomorphic mutations) still remains sufficient to go through the early developmental process because of its adaptive plasticity or rather heterozygote advantage. However, in some cases, such partial loss-of-function of genes compromise normal homeostasis due to haploinsufficiency later in adult life having many environmental stress challenges. By contrast, any heterozygote-advantageous genes might gain a certain benefit(s) (much more fitness) by such partial loss-of-function later in life. Physiological senescence may evolutionarily arise from both genetic and epigenetic drifts as well as from losing adaptive developmental plasticity in face of stress signals from the external environment that interacts with functions of multiple genes rather than effects of only a single gene mutation or defect. Previously uncharacterized developmental genes may thus mediate the aging process and play a pivotal role in senescence. Moreover, unexpected senescence-related genes might also be involved in the early developmental process and regulation. We wish to ascertain whether we can identify such genes promptly in a comprehensive manner. The ease of manipulation using the zebrafish system allows us to conduct an exhaustive exploration of novel genes and small molecular compounds that can be linked to the senescence phenotype and thereby facilitates searching for the evolutionary and developmental origins of aging in vertebrates. Birth Defects Research (Part C) 93:229–248, 2011. © 2011 Wiley-Liss, Inc.