So was it so hard to admit that you were wrong?
>
> I agree that duplications of large chromosomal segments of yeast have been observed in the lab. Thank
> you for the information.
> Does this mean that these duplications were INHERITED, then became FIXED IN POPULATIONS, in order
> for them to mutate into new, different instruction sets for building new proteins?
They are inherited just like any other mutation in your genome. You
have gene duplications that you have a chance of passing onto your children.
As the paper that I gave you indicates there is a difference in that
tandem duplications have a higher back reversion rate than their forward
mutation rate. This just means that duplications can be undone more
often than other mutations like base substitutions that would basically
have the same reversion rate as their mutation rate. The paper notes
that this higher reversion rate is nullified by translocating the
duplicated sequence to another chromosome, and this was also observed by
the researchers, so that they could do the analysis and come to that
conclusion.
I talked about this elevated reversion rate in another thread somewhere.
It is due to aberrant recombination. Genetic recombination happens
every meiosis at a certain frequency, and if the duplicated segments do
not match up correctly you can lose a copy. You can also gain a copy.
That is why we can explain things like the HOX tandem duplication. We
have observed how you gain and lose duplicated copies.
As other mutations can be fixed in the population so can duplications.
Neutral mutations are fixed basically at the rate of mutation, but if
the duplication has a selective advantage like the duplications of
starch metabolizing genes that you likely have if you are of Asian or
European descent (an adaptation to cereal grain agriculture) they can
increase rapidly in a population due to positive selection.
>
> As the above quote FROM YOUR PAPER demonstrates, YOU DON'T KNOW.
What don't we know?
>
> So why have you been beaking off about how gene duplications PRODUCE NOVEL FUNCTIONS AND
> STRUCTURES IN ORGANISMS?
>
Eddie, remember that estrogen receptor paper that you talked about in
one of your threads. There was a gene duplication, one copy acquired
two new mutations that altered the active site and allowed the receptor
to recognize a new hormone, both hormone receptors have duplicated many
times and do multiple different things in extant organisms. What don't
you understand. How do you think that the researchers were able to
backtrack and figure out the original protein sequence.
You were using that paper as an example of where two mutations were
required, but as Behe himself calculated those two mutations may have a
low probability of occurring, but would be expected to occur among the
number of organisms in a cubic meter of pond mud every generation.
Remember that calculation that came out during the Dover testimony?
The tRNA synthases required to make proteins are all duplicated from
just two original synthases, do you remember that example?
This is the type of real science that you are up against, and why ID is
just a scam.
Apologize for lying about me to another poster. You will likely feel
better about your lousy pathetic self. Just look at the pathetic junk
that you have resorted to doing, and you know that you were lying.
Ron Okimoto