From: Rafal Smigrodzki (rafal@smigrodzki.org)
Date: Tue Apr 22 2003 - 19:23:46 MDT
Robert wrote:
>
> So one could design an additional chromosome based on EBV where
> all (most?) of the EBV genes are replaced with recoded mito genes.
> Then one extracts the most primitive stem cells one can find
> in the body, infects them with the anti-aging EBV-based therapy
> vector then amplifies the # you have and puts the modified stem
> cells back into the body.
>
### No need to - two groups have recently developed methods of transfecting
full-length mito genomes into mitos, so you can go there directly.
One of these guys was rejected by a prominent journal after showing
*mitochondria glowing with GFP* transcribed from the mtDNA! The reviewer
reportedly simply commented on the photographs "This can't be true".
Un-****ing-believable.
But anyway, it is indeed possible to replace full length mtDNA now, so it's
just a matter of time before somebody manages to do something useful with
it.
Rafal
This archive was generated by hypermail 2.1.5 : Tue Apr 22 2003 - 16:32:54 MDT