On 8/1/2014 3:30 PM, Steady Eddie wrote:
> On Friday, 1 August 2014 13:13:44 UTC-6, Greg Guarino wrote:
>> On 8/1/2014 2:46 PM, Steady Eddie wrote:
>>
>>
>>
>>> Why would NEUTRAL mutations be passed on to that individual's offspring?
>>
>>
>>
>> I likely have at least several dozen mutations in my DNA; "letters" that
>>
>> do not match either my mother's or father's genome at those sites. None
>>
>> of them were fatal, and none of them have prevented me from reproducing.
>>
>>
>>
>> Even though we could describe those mutations as "copying errors", they
>>
>> are nonetheless part of my genome now; copied (mostly) faithfully
>>
>> trillions of times into the cells in my body, notably including my sperm
>>
>> cells.
>>
>>
>>
>> What would prevent (some of) those mutations from being passed on to my
>>
>> offspring? "Selection" is no answer, as I have successfully reproduced.
>>
>> Statistically speaking, roughly half a parent's mutations should be
>>
>> inherited by each child.
>
> Yes, then half of that in the next generation, until your particular mutations exponentially approach zero.
> Meaning, as your progeny continues to reproduce, your particular mutations get CANCELLED OUT
> quite quickly by the original genome in the population (unless, in the case of the wild, a mutation
> confers an evolutionary advantage).
I was going to post a one-liner about just how profoundly you're
misunderstanding things but that's pointless.
Please think on what you wrote here. You are NOT describing something
that's "unselected" (as you wrote in a different post). You are
describing (without realizing it) a mutation under significant selection
pressure- probably more powerful selection pressure than you'd ever see
in the wild, other than for a lethal dominant allele.
Remember when you asked where Ernest Major got that number 10E-08? This
is where it where it comes into play. 10E-08 seems to be a pretty good
estimate of the mutation rate in eukaryotes. So every individual born,
hatched, whatever, has a number of mutations. Some number of these are
deleterious (but NOT lethal, please remember that for later), most are
neutral, and a very few might be beneficial.
Let's stick to the mutations that are neutral. Do you know how a
mutation can be neutral? A moment's calculation will tell you there are
64 possible combinations of the four nucleotides (adenine, guanine,
cytosine, thymine) that make the DNA triplets- each triplet codes for a
particular amino acid. One triplet codes for AUG, the "start" codon, and
three code for "stop" codons, so there's actually 60 triplets for 20
amino acids (AUG also codes for methionine, so line up quick for pedant
points...)
This allows for some redundancy. Many amino acids will be produced by
more than one triplet. Proline is an example. Proline is coded for by
several DNA triplets, including GGG and GGT. So we could have a mutation
in a DNA triplet, changing G to T or vice versa, and it's completely
neutral.
Another way to get a neutral mutation becomes obvious when you look at
the structure of enzymes. Most enzymes are pretty large proteins. The
most critical region is the binding site, where the substrate attaches.
A change in an amino acid there is likely to alter or even wreck the
function of the enzyme- the substrate just won't be able to bind there
anymore. Second, the enzyme has to have a particular shape to it. Ever
hear the phrase "form follows function"? It's true with a vengeance in
enzymes. The shape is determined by other "levels" of protein structure,
in particular things like van der Waal's forces and disulfide bonds
between amino acids that are distant from the binding site. A change
here is slightly less likely to result in change or loss of function,
but mutations can be serious. Sickle-cell disease is an example: the
mutation is not a change at the oxygen binding site, but the molecular
structure is altered such that the hemoglobin is liable to collapse if
it is depleted of oxygen too rapidly, causing the erythrocyte to change
shape or "sickle".
Now, neutral mutations are not "cancelled out" by the population's
genome. There's a real chance that a mutation will be lost due to drift
("dumb luck" as you correctly put it). Remember- an organism might die
without progeny, and even if it does reproduce, there's only a 50%
chance that the mutation will be inherited by any given one of its
offspring. But neutral mutations are accumulated over time. Heck,
compare how long it takes to eliminate a _lethal_ recessive allele from
a population and it becomes obvious that _neutral_ recessive mutations
are just going to stick around forever.
How do they accumulate, you ask? Well, they just keep happening, over
and over and over again. 10E-08, remember? How many nucleotides do you
have in your genome? On average, we've all got about a dozen mutations
that we're stuck with, and that doesn't even include the ones that
happened in our parents, grandparents, great-grandparents etc. If you
have any kids, each one will get about 6 of your mutations, and have a
dozen of their own. Most are neutral, some might be deleterious, and
some might be beneficial. Some might be back-mutations that actually
revert an earlier mutation to its previous state.
Now, why did I say to remember the difference between deleterious and
lethal? Lethal alleles are obviously a subset of deleterious alleles,
but by no means are they the whole of the set. Too many people equate
the two, and as we see in sickle-cell disease (and for that matter
Huntington's disease, a lethal _dominant_ disorder, although there's a
complicating factor there) even a disease that can kill you will not
necessarily prevent you from reproducing. "Deleterious" in the sense of
population genetics really just means "reduced fertility" or "lower
reproductive success". Might kill you, might not, but on average, you'll
have _fewer_ surviving progeny than someone not carrying that particular
allele or pair of alleles, but probably not _zero_ progeny.
This obviously applies to Behe's work, and I have not seen anyone bring
it up yet. A mutation may very well be deleterious (the mutations in
_Plasmodium_ were apparently neutral, or nearly so) but so what? Unless
it's a lethal dominant allele, it is NOT going to be removed from the
population by selection in a single generation.It might persist for a
very long time indeed.
And if it is a deleterious recessive allele, its very rarity will help
it persist, wrt selection, at least. If it's recessive, it will not
exert deleterious effects unless it is paired with another copy of the
mutation- and that means it's highly unlikely to be exerting any
ill-effects on the organism's reproductive success.
This is why inbreeding/incest can have consequences. It's not so much
that one person might be a mutant- we're all mutants. But the more
closely related you are to your mate, the more likely it is that you're
carrying the SAME deleterious recessive alleles, rather than a
completely different set.
Chris