By studying yeast cells, researchers have managed to ‘slow ageing’ by building a biosynthetic genetic clock to extend lifespan
Human lifespan is related to the ageing of our individual cells. Three years ago a group of University of California San Diego researchers deciphered essential mechanisms behind the aging process.
After identifying two distinct directions that cells follow during ageing, the researchers genetically manipulated these processes to extend the lifespan of cells.
They have now extended this research using synthetic biology to engineer a solution that keeps cells from reaching their normal levels of deterioration associated with ageing.
Cells, including those of yeast, plants, animals and humans, all contain gene regulatory circuits that are responsible for many physiological functions, including ageing.
Professor Nan Hao, of the School of Biological Sciences’ Department of Molecular Biology, the senior author of the study and co-director of UC San Diego’s Synthetic Biology Institute, said: “These gene circuits can operate like our home electric circuits that control devices like appliances and automobiles.”
However, the UC San Diego group uncovered that, under the control of a central gene regulatory circuit, cells don’t necessarily age the same way.
Imagine a car that ages either as the engine deteriorates or as the transmission wears out, but not both at the same time.
The UC San Diego team envisioned a ‘smart ageing process’ that extends cellular longevity by cycling deterioration from one ageing mechanism to another.
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Stall the ageing process
In the new study, the researchers genetically rewired the circuit that controls cell ageing. From its normal role of functioning like a toggle switch, they engineered a negative feedback loop to stall the ageing process.
The rewired circuit operates as a clock-like device, called a gene oscillator, that drives the cell to periodically switch between two detrimental ‘aged’ states, avoiding prolonged commitment to either, and thereby slowing the cell’s degeneration.
These advances resulted in a dramatically extended cellular lifespan, setting a new record for life extension through genetic and chemical interventions.
As electrical engineers often do, the researchers in this study first used computer simulations of how the core ageing circuit operates.
This helped them design and test ideas before building or modifying the circuit in the cell. This approach has advantages in saving time and resources to identify effective pro-longevity strategies, compared to more traditional genetic strategies.
Hao said: “This is the first time computationally guided synthetic biology and engineering principles were used to rationally redesign gene circuits and reprogramme the ageing process to effectively promote longevity.”
Cascade of molecular changes
Several years ago, the multidisciplinary UC San Diego research team began studying the mechanisms behind cell ageing, a complex biological process that underlies human longevity and many diseases.
They discovered that cells follow a cascade of molecular changes through their entire lifespan until they eventually degenerate and die. But they noticed that cells of the same genetic material and within the same environment can travel along distinct ageing routes.
About half of the cells age through a gradual decline in the stability of DNA, where genetic information is stored. The other half ages along a path tied to the decline of mitochondria, the energy production units of cells.
The new synthetic biology achievement has the potential to reconfigure scientific approaches to age delay.
Distinct from numerous chemical and genetic attempts to force cells into artificial states of ‘youth’, the new research provides evidence that slowing the ticks of the ageing clock is possible by actively preventing cells from committing to a pre-destined path of decline and death, and the clock-like gene oscillators could be a universal system to achieve that.
The researchers said: “Our results establish a connection between gene network architecture and cellular longevity that could lead to rationally designed gene circuits that slow ageing.”
Unbiased genetic screens
During their research, the team studied Saccharomyces cerevisiae yeast cells as a model for the ageing of human cells. They developed and employed microfluidics and time-lapse microscopy to track the ageing processes across the cell’s lifespan.
In the current study, yeast cells that were synthetically rewired and aged under the direction of the synthetic oscillator device resulted in an 82% increase in lifespan compared with control cells that aged under normal circumstances.
The results revealed: “the most pronounced lifespan extension in yeast that we have observed with genetic perturbations.”
Hao added: “Our oscillator cells live longer than any of the longest-lived strains previously identified by unbiased genetic screens.”
The authors concluded: “Our work represents a proof-of-concept example, demonstrating the successful application of synthetic biology to reprogramme the cellular ageing process, and may lay the foundation for designing synthetic gene circuits to effectively promote longevity in more complex organisms.”
The team is currently expanding their research to the ageing of diverse human cell types, including stem cells and neurons.
The research is published in Science.
Image: Engineered cells show oscillating abundance of a master ageing regulator. © Hao Lab, UC San Diego.
