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Posted by: kingmilk at Mon Feb 7 21:16:05 2005 [ Email Message ] [ Show All Posts by kingmilk ] I did mention something to that effect, but I don't think my original point was ever understood. What I intended to express was that the level of testing that was available two years ago, and three years before that time when I was looking at haplotypes in Gallus domestics, could not have revealed more subtle differences. There may in time be techniques that could really reveal on a molecular level, a hybrid event, for many many generations to come. At this time, we are nowhere near that. Thus, "masking" genetic differences can be accomplished through "backbreeding", which is taking the hybrid f1 back to one of the parent forms and then going in that direction for generations. In some of our very simple tests, for instance MtDNA, this factor can be manipulated in this manner. For instance, if you take your male f1 hybrid and breed it back to the female of the species whose MtDNA you want represented, you will then pick up that MtDNA and all that generation will show the MtDNA of the special form in question. This does not mean that this animal is then "pure", but that on the MtDNA level, it would be indistinguishable from "pure" forms of the MtDNA line. For instance, in laymans terms, if I choose to make a jungle corn and I breed a male cal to a female corn, I get f1 hybrid, junglecorn which has MtDNA of corn, but is 50% genetic material from each parent. If I want my MtDNA to say "cal", then you take the f1 jungle (corn MtDNA) back to a female cal and all those offspring show "cal MtDNA". This always works this way and shows the limits of MtDNA as a major marker factor in genetic work. It is in the nuclear DNA that the real story is happening. Except for the sex-linked genes at the X and Y chromosomes, all these genes are based on the many, many alleles on the chromosomes. You get one half of your total package from each parent, so the first thing to consider is that closely related lifeforms (and these snakes which can produce fertile offspring definately are closely related) may share almost all of their genetic material in common. We share 98% with chimpanzees, so imagine how much closer it is in say ratsnakes and cornsnakes or the various forms of getula. Thus you really dont have that many variable alleles. The variations at thsoe alleles may be great, especially depending upon the distance in time from species split behind the two forms, but those which can produce complete fertility in their f1 offspring are not very differentiated , thus probably not very far apart in time, as their seperate evolution goes. Thus you would require a complete gene map of each parent species (as has just recently been finished in humans and poultry, at considerable expenses)to look for any variations in the genome. This would then be your markers. It is by looking for markers that genetic difference is notated. Back breeding and selection can allow you to go back to complete genetic "purity" (i.e., a complete match to the original genome of either parent form) by using molecular markers in each generation to narrow and weed out the genes remaining from the alternate parent forms. However, this would require access to a full mapping of both original species and the ability to map the offspring for comparisonin each generation. At our current level of knowledge we could accomplish this. However, applying it to our hobby animals is unlikely, as this is an very costly process. | ||
>> Next Message: thanks so much Kingmilk! more.. - bluerosy, Tue Feb 8 10:37:07 2005 | ||
<< Previous Message: question for Kingmilk - bluerosy, Mon Feb 7 13:32:04 2005 |
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