Related Experiment Video
Updated: Jun 30, 2026

10:39
A Suppressor Screen for the Characterization of Genetic Links Regulating Chronological Lifespan in Saccharomyces cerevisiae
Published on: September 17, 2020
When can a clonal organism escape senescence?
1Center for Population Biology, University of California, Davis, California 95616, USA.
The American Naturalist
|September 25, 2008
Summary
Clonal organisms may escape senescence by replacing old modules with new ones. Declining reproduction and survival rates increase the likelihood of senescence in clones, impacting their long-term survival.
Area of Science:
- Ecology
- Evolutionary Biology
- Gerontology
Background:
- Clonal organisms exhibit diverse life spans, with some living for millennia without senescence and others having finite lifespans.
- Understanding the factors driving senescence or its absence in clonal organisms is crucial for ecological and evolutionary studies.
Purpose of the Study:
- To investigate how life-history rates of individual modules within a clone influence the senescence of the genetic individual.
- To determine the conditions under which clonal organisms escape or succumb to senescence.
Main Methods:
- Development and application of two theoretical models to simulate clonal life-history dynamics.
- Utilizing a modified matrix model to represent the clonal lifestyle and analyze trade-offs.
Main Results:
- Senescence is more likely when clonal reproduction, sexual reproduction, and module survival rates decline with age.
- A decline in sexual reproduction rate with clone age is a more common indicator of senescence than increased mortality.
- Trade-offs between sexual and clonal reproduction can drive selection for or against clonal senescence.
Conclusions:
- Clonal senescence is influenced by the interplay of module-stage-specific life-history rates and reproductive strategies.
- Selection on life-history traits can increase with clone age, potentially counteracting senescence evolution in growing populations.
- The study provides insights into the evolutionary persistence of clonal organisms and the mechanisms underlying aging in modular life forms.
Related Concept Videos
Replicative Cell Senescence
Replicative cell senescence is a property of cells that allows them to divide a finite number of times throughout the organism's lifespan while preventing excessive proliferation. Replicative senescence is associated with the gradual loss of the telomere — short, repetitive DNA sequences found at the end of the chromosomes. Telomeres are bound by a group of proteins to form a protective cap on the ends of chromosomes. Embryonic stem cells express telomerase — an enzyme that adds the telomeric...
Replicative Cell Senescence
Replicative cell senescence is a property of cells that allows them to divide a finite number of times throughout the organism's lifespan while preventing excessive proliferation. Replicative senescence is associated with the gradual loss of the telomere — short, repetitive DNA sequences found at the end of the chromosomes. Telomeres are bound by a group of proteins to form a protective cap on the ends of chromosomes. Embryonic stem cells express telomerase — an enzyme that adds the telomeric...
Reproductive Cloning
Reproductive cloning is the process of producing a genetically identical copy—a clone—of an entire organism. While clones can be produced by splitting an early embryo—similar to what happens naturally with identical twins—cloning of adult animals is usually done by a process called somatic cell nuclear transfer (SCNT).
Somatic Cell Nuclear Transfer
In SCNT, an egg cell is taken from an animal and its nucleus is removed, creating an enucleated egg. Then a somatic cell—any cell that is not a sex...
Somatic Cell Nuclear Transfer
In SCNT, an egg cell is taken from an animal and its nucleus is removed, creating an enucleated egg. Then a somatic cell—any cell that is not a sex...
Reproductive Cloning
Reproductive cloning is the process of producing a genetically identical copy—a clone—of an entire organism. While clones can be produced by splitting an early embryo—similar to what happens naturally with identical twins—cloning of adult animals is usually done by a process called somatic cell nuclear transfer (SCNT).
Somatic Cell Nuclear Transfer
In SCNT, an egg cell is taken from an animal and its nucleus is removed, creating an enucleated egg. Then a somatic cell—any cell that is not a sex...
Somatic Cell Nuclear Transfer
In SCNT, an egg cell is taken from an animal and its nucleus is removed, creating an enucleated egg. Then a somatic cell—any cell that is not a sex...
Cells of the Adaptive Immune Response
The T and B lymphocytes of the adaptive immune system develop from common lymphoid progenitor cells in the bone marrow. These progenitors give rise to precursors that eventually develop into both T and B lymphocytes. As these precursors mature, they gain the ability to detect and respond to foreign antigens in the body, a process known as immunocompetence. Additionally, these precursors acquire self-tolerance, a process that ensures they do not react to self-antigens. This intricate system...
Maintenance of the ES Cell State
The cells of the blastocyst inner cell mass only remain pluripotent for a short time. This state of pluripotency and self-renewal can be maintained in embryonic stem (ES) cell culture by adding specific chemicals or growth factors to ensure the cells can continue dividing and later differentiate into different cell types. In some cases, the cells are grown on a feeder layer of differentiated cells, which provides the growth factors and extracellular matrix components necessary for stem cell...

