Ruckus
Well-known member
True in itself, but it isn't relevant to the point I was making.There is no way for a body to know which genes it's closely related to vs. when it is not. It can't run an evolutionary tree and make that type of determination. I mean you and an apple probably share about half your genes. It's all just combinations of ACGT. Very simple changes - including a SINGLE BASE change can result in radically different product (we know very serious diseases where the difference between a perfectly healthy person and an extremely sick one is a single base pair change - one G to C or something like that). So there is very little advantage to being 'close'. In fact, it's probably a disadvantage, because a single mutation can sometimes create a product that's very similar in some ways (e.g it can interact with lots of things in the body it used to) but is in fact much worse - because now it stops the activity of all the things it used to interact with.
The point I was making was to do with the presence of "correlated gene arrangements" in organisms. An example of this are things called Hox genes which "are a group of related genes that determine the basic structure and orientation of an organism". They're basically a highly conserved group of genes that serve an overall common function. If any of the genes within the 'set' is disrupted, it can lead to significant changes. The genome of an organism is more than just a collection of individual genes operating in isolation - it's an arrangement of individual genes and related gene groups which interact in complex ways. And the point about 'inserting a gene correctly' is very relevant here too. I think it's one of the main issues raised with GE. Some of the studies I read indicated that there have been cases where recDNA has been inserted into the 'functional' part of a gene/gene group, silencing it's expression. Or alternatively, sometimes additional, unintended, genetic material is inserted with the intended DNA interrupting other sequences. I would imagine these kind of things wouldn't occur very often via natural processes. But, really, it's a point of concern, but the solution is obviously just to make sure the methods used are sound, and there is a complete understanding of where the gene is being inserted and the surrounding genes. Not insurmountable problems by any means, but ones that would require evaluation on a case-by-case basis.Yes, there are many regulatory genes - but I am not sure what that has to do with anything. If we insert a gene correctly, the regulatory genes will express that gene and we'll have a product (e.g Vitamin A). Or it might not be expressed, or expressed at a lower rate, and then we might have no (or very little) Vitamin A.
The thrust that I think you're making - that somehow the interaction of genes may create a bran new unexpected metabolite different, and yet dangerous, and yet would simply not be detected in a chemical analysis is pretty unlikely. Or rather, as I said, I don't know by what mechanism such a thing would be more likely than cross breeding species.