Ä Area: 190 ÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄ
Msg#: 4 Date: 10 Nov 97 06:33:06
From: Surgical Steel
To: All
Subj: And still more...
ÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄÄ
Same disclaimer, etc.
-> E1> How would this happen, then? Mutations do more bad than good, and breedi
-> E1> by cloning isn't really going to expand your gene pool. And how long did
-> E1> the Earth Exist again, if this took billions of years?
-> It depends entirely where the mutation occurs in the DNA sequence as to
-> the result; due to the unpredictable nature of mutations, especially in mor
-> complex and interdependent organisms such as vertebrates, any significant
-> mutation stands a greater chance of messing up an already existant trait.
-> However, considering that you (yes, YOU) are undoubtedly a mutation yourself
-> I'm not so sure that you have a good idea of what exactly a mutation *is*.
-> To sum up, just remember your words the next time you get hit by a
-> penicillin-resistant bacterium, and tell them that they aren't able to do th
->
-> Oh - and I said "millions (if not billions) of years". It would really
-> depend on what he was talking about as a start and end point, and to be hone
-> I don't have a timeline in front of me at present.
>Ah, let's put it this way. Most mutations are bad. If a carpenter
>cemented ONE good brick for every 1000 bad ones, the house would
>surely collapse.
Given your analogy, yes. However, you are not accurately
describing what happens when there is a mutation - perhaps the
RESULT of a mutation, but not the mutation itself.
As I said before, YOU ARE A MUTANT. There are mutated cells in
your body *right now*.
We'll address this more after this next bit...
>Also, in fruit fly experiments, the second generation 'mutants'
>reverted back into normal fruit flies.
Of course - this is in keeping with basic Mendelian genetics.
Let me demonstrate with some basic Mendelian squares.
(yes, this is long, but this is EXACTLY what you said you wanted
- a basic explanation, even if it *is* more than 80 lines. But
I'm sure you want to understand, so I'm not worrying about it.)
Although for this first example, I'm presuming that the mutation
was a recessive, that bears out with the experimental results
above. Results when the mutation is a dominant follow as well.
M = non-mutated, dominant genet m = mutated recessive gene
| M | M |
----|-------|------| Here we have a mutant (double recessive)
m | Mm | Mm | fruit fly mating with a (double dominant)
----|-------|------| "normal" fruit fly. As you can see, all of
m | Mm | Mm | the offspring would *appear* normal, but
----|-------|------| they are carriers of the mutated gene.
| M | M | Here, our second-generation fruit fly mates
---|-------|------| with a "normal" fruit fly - yet all the
m | Mm | Mm | offspring still appear normal - and 50% of
---|-------|------| them ARE double dominant "normal" flies!
M | MM | MM |
----|-------|------|
| M | m | It is only here, where we crossbreed two
----|-------|------| of the "carriers" together that we have
M | MM | Mm | any chance at all (approx. 25% here) of
----|-------|------| the mutation being expressed - and we ALSO
m | Mm | mm | have a 25% chance of a fully "normal" fly
----|-------|------| being the result!
Things change somewhat when the mutation is a dominant gene:
M = dominant MUTANT gene m = recessive "normal" gene
| m | m | Looks familiar, right? Thing is that all of
----|-------|------| these offspring are phenotypically MUTANTS.
M | Mm | Mm | However, they all also carry the "normal"
----|-------|------| gene... (I'm only going to do the cross
M | Mm | Mm | breeding square below, I'm sure you've got
----|-------|------| the hang of how to do this by now...)
| M | m | We're back to the 1:2:1 split - one "full"
----|-------|------| mutant, two "carriers" (though in this example
M | MM | Mm | they "look" mutant), and one NORMAL fruit
----|-------|------| fly - in the second generation!
m | Mm | mm |
----|-------|------|
This sort of thing is why some traits "skip generations" in
humans - pattern baldness, cancer, and the like.
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