Shane Costello
Graduate Poster
- Joined
- Aug 8, 2001
- Messages
- 1,232
Originally posted by athon:
Ok, but if a sequence is conserved across two species, why would you transfer it? If it doesn't exist in one species, and you wish to place a coding sequence into a crop that does not possess it, how can you initially be certain that it does not have a different effect?
Well the gene may be active in one species but inactive in another, the difference being in the activity of regulaory elements. Initially you wouldn't be certain that it wouldn't have a different effect, hence the reason for field trials and a regulatory framework. At the risk of sounding like a broken record this should actually an argument in favour of GM. Conventional breeding involves the transfer of entire genomes, while GM involves the transfer of no more than a few genes. The potential for "different effects" is far greater with conventional breeding.
As for non-coding sequences, we are only just beginning to understand how complicated that issue is. Granted, it has not been attempted yet in commercial GM (to my knowledge, but I could be shown wrong), but the temptation will surely arise to use an amplifier sequence or play with promoter regions to increase yields. At the moment it is rather crude manipulation of coding sequences that produce extra growth.
I believe it's already being done. I'll have to do a bit of googling but I worked with transgenic apple plants for a while. These had been transformed with a phytohormone gene with a bacterial promoter, with the ultimate effect of prolonging shelf life.
It is definately not a simple 'take gene A from species A and it will do the same thing next to gene B in species B'. Initially the industry thought it would, and with early GM in bacteria it was as simple as that. But eukaryotic organisms are proving to have a lot of tricks to get past.
I think it depends on the specific gene and the trait it influences. Some traits are complex, and influenced by a number of genes, other traits are simple and influenced by the expression of single genes. It's not true to say that early GM in bacteria was simple. Horizontal gene transfer of genes between bacteria is a natural phenomenon, so splicing bacterial genes in bacterial genomes is an easy process in vitro. However in the case of human insulin the human insulin gene (eukaryote) was spliced into an E.coli strain (prokaryote). This is not an easy process, since prokaryotic genomes lack the promoter sequences required by eukaryotic genes.