Find the genetic difference to longevity between architecture compared with maintenance
Swap all the homeobox developmental genes of mouse with beaver or bat to create mouse maintenance of beaver as well as beaver maintenance of mouse
If architecture is more prevelant as a longevity source then the slight 1 to 5 pct genetic variation between the beaver as well as the mouse is a gene area giving 10 or 20 times greater longevity
Bringing that greater longevity to humans. Find similar sequence variations as those at the beaver mouse variations at database sequences of primates to humans. siRNA or gene therapy is created to amplify the lifespan of existing as well as new humans based on the particular mRNA that the genes code. With more research just update the human genome to give all humans superlongevity.
Note that if maintenance is the longevity source then those chemicals genetically coded (DNA -> mRNA -> protein -> other molecules) that produce maintenance can be produced as longevity drugs.
Part of the value of longevity research
The value is comparable to the difference (young-old) productivity times value of the world economy Thus if 2010 world GDP is 80 trillion US$ then this research produces 10 to 100 pct of that value as the young human quality productivity increases so 8 or 80 trillion US$ of value each year from the application of this research. Thus if the very basic beaver mouse comparison research is $100,000$ to $1 million to prove effect, that is over a million pct return on $. A million pct return may motivate the private sector to fund this research as well as a variety of nations.
