by Tanada » Sat 29 May 2010, 12:23:56
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Surely that is a possibility, however it remains to be seen, would such modified mitochondria be reconcilable with functions of mammalian cell.
In any case human life span is already rather long (comparable to birds with supposedly better mitochondria) and free radical damage is not the only factor responsible for aging of human cells.
What about telomer loss for example?
And try to fiddle with telomerase too much and cancers will result.
Certainly, though I can't find the link I know I have read articles on cross species mDNA transfer. The issue came up due to cloning research, if you use for example a cow ovum for a sheep clone the sheep clone has the cow mother's mDNA in all of its cells instead of the donor sheep's mDNA. It has been suggested that R&D should be done to see just how far the cross compatibility extends. For example if you could use unfertilized fish eggs as donor ova you could manipulate them much more easily than mammalian donor eggs due to their larger size. This raised the issue of what effect fish mDNA would have on mammalian clone development.
My post was in reference to the fact that an mDNA strand is much simpler than many bacteria DNA sequences, though I do not know the specifics of the edited synthetic cell referred too in the experiment that started this thread. It stands to reason that if this technology could be used to create synthetic mDNA strands that resemble those in longer lived life forms but which are compatible to mammals it will be done, sooner or later.
What ultimate life expectancy could result? I do not know, and I doubt anyone else does either, however it is contended that free radicals produced by mDNA contribute to the aging process. Logic dictates that removing this source of free radicals would have a slowing effect on the aging process. See
http://www.circuitblue.com/biogerontology/mito.shtml for some suggestions of how it might work.