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Selection at one locus with many alleles, fertility selection, and…
Tags: abo blood group, aj, allele, array, equilibrium, fertility, genotype, genotypes, hardy weinberg principle, heterozygotes, ities, locus, matrix, multiple alleles, pi, pj, sexual selection, viability, w12, w22,Pages: 7
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Created: Mon Aug 25 09:26:20 2008
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Selection at one locus with many alleles,
fertility selection, and sexual selection
Introduction
It's easy to extend the Hardy-Weinberg principle to multiple alleles at a single locus. In fact,
we already did this when we were discussing the ABO blood group polymorphism. Just to
get some notation out of the way, though, let's define xij as the frequency of genotype Ai Aj
and pi as the frequency of allele Ai . Then
p2
i if i = j
xij =
2pi pj if i = j
Unfortunately, the simple principles we've learned for understanding selection at one locus
with two alleles don't generalize completely to selection at one locus with many alleles (or
even three).
· For one locus with two alleles, heterozygote advantage guarantees maintenance of a
polymorphism.
· For one locus with multiple alleles, there are many different heterozygote genotypes.
As a result, there is not a unique pattern identifiable as "heterozygote advantage,"
and selection may eliminate one or more alleles at equilibrium even if all heterozygotes
have a higher fitness than all homozygotes.
Selection at one locus with multiple alleles
When we discussed selection at one locus with two alleles, I used the following set of viabil-
ities:
A1 A1 A1 A2 A2 A2
w11 w12 w22
c 2001-2008 Kent E. Holsinger
You can probably guess where this is going. Namely, I'm going to use wij to denote the
viability of genotype Ai Aj . What you probably wouldn't thought of doing is writing it as a
matrix
A1 A2
A1 w11 w12
A2 w12 w22
Clearly we can extend an array like this to as many rows and columns as we have alleles so
that we can summarize any pattern of viability selection with such a matrix. Notice that I
didn't write both w12 and w21 , because (normally) an individual's fitness doesn't depend on
whether it inherited a particular allele from its mom or its dad.1
Marginal fitnesses and equilbria
After a little algebra it's possible to write down how allele frequencies change in response to
viability selection:2
pi w i
pi = ,
w¯
where pi = pi wij is the marginal fitness of allele i and w = p2 wii + i j>i 2pi pj wij is
¯ i
the mean fitness in the population.
It's easy to see3 that if the marginal fitness of an allele is less than the mean fitness of
the population it will decrease in frequency. If its marginal fitness is greater than the mean
fitness, it will increase in frequency. If its marginal fitness is equal to the mean fitness it
won't change in frequency. So if there's a stable polymorphism, all alleles present at that
equilibrium will have marginal fitnesses equal to the population mean fitness. And, since
they're all equal to the same thing, they're also all equal to one another.
That's the only thing easy to say about selection with multiple alleles. To say anything
more complete would require a lot of linear algebra. The only general conclusion I can
mention, and I'll have to leave it pretty vague, is that for a complete polymorphism4 to
be stable, none of the fitnesses can be too different from one another. Let's play with an
example to illustrate what I mean.
1
If it's a locus that's subject to genomic imprinting, it may be necessary to distinguish A1 A2 from A2 A1 .
Isn't genetics fun?
2
If you're ambitious (or a little weird), you might want to try to see if you can derive this yourself.
3
At least it's easy to see if you've stared a lot at these things in the past.
4
A complete polymorphism is one in which all alleles are present.
2
An example
The way we always teach about sickle-cell anemia isn't entirely accurate. We talk as if
there is a wild-type allele and the sickle-cell allele. In fact, there are at least three alleles at
this locus in many populations where there is a high frequency of sickle-cell allele. In the
wild-type, A, allele there is a glutamic acid at position six of the chain of hemoglobin. In
the most common sickle-cell allele, S, there is a valine in this position. In a rarer sickle-cell
allele, C, there is a lysine in this position. The fitness matrix looks like this:
A S C
A 0.976 1.138 1.103
S 0.192 0.407
C 0.550
There is a stable, complete polymorphism with these viabilities:
pA = 0.83
pS = 0.07
pC = 0.10 .
If allele C were absent, A and S would remain in a stable polymorphism:
pA = 0.85
pS = 0.15
If allele A were absent, however, the population would fix on allele C.5
The existence of a stable, complete polymorphism does not imply that all subsets
of alleles could exist in stable polymorphisms. Loss of one allele as a result of
random chance could result in a cascading loss of diversity.6
If the fitness of AS were 1.6 rather than 1.103, C would be lost from the population, although
the A - S polymorphism would remain.
Increasing the selection in favor of a heterozygous genotype may cause selection
to eliminate one or more of the alleles not in that heterozygous genotype. This
also means that if a genotype with a very high fitness in heterozygous form is
introduced into a population, the resulting selection may eliminate one or more
of the alleles already present.
5
Can you explain why? Take a close look at the fitnesses, and it should be fairly obvious.
6
The same thing can happen in ecological commmunities. Loss of a single species from a stable community
may lead to a cascading loss of several more.
3
Fertility selection
So far we've been talking about natural selection that occurs as a result of differences in the
probability of survival, viability selection. There are, of course, other ways in which natural
selection can occur:
· Heterozygotes may produce gametes in unequal frequencies, segregation distortion, or
gametes may differ in their ability to participate in fertilization, gametic selection.
· Some genotypes may be more successful in finding mates than others, sexual selection.
· The number of offspring produced by a mating may depend on maternal and paternal
genotypes, fertility selection.
In fact, most studies that have measured components of selection have identified far larger
differences due to fertility than to viability. Thus, fertility selection is a very important
component of natural selection in most populations of plants and animals. As we'll see a
little later, it turns out that sexual selection is mathematically equivalent to a particular
type of fertility selection. But before we get to that, let's look carefully at the mechanics of
fertility selection.
Formulation of fertility selection
I introduced the idea of a fitness matrix earlier when we were discussing selection at one
locus with more than two alleles. Even if we have only two alleles, it becomes useful to
describe patterns of fertility selection in terms of a fitness matrix. Describing the matrix is
easy. Writing it down gets messy. Each element in the table is simply the average number of
offspring produced by a given mated pair. We write down the table with paternal genotypes
in columns and maternal genotypes in rows:
Paternal genotype
Maternal genotype A1 A1 A1 A2 A2 A2
A1 A1 F11,11 F11,12 F11,22
A1 A2 F12,11 F12,12 F12,22
A2 A2 F22,11 F22,12 F22,22
Then the frequency of genotype A1 A1 after one generation of fertility selection is:7
x2 F11,11 + x11 x12 (F11,12 + F12,11 )/2 + (x2 /4)F12,12
11 12
x11 = ¯ , (1)
F
7
I didn't say it, but you can probably guess that I'm assuming that all of the conditions for Hardy-
Weinberg apply, except for the assumption that all matings leave the same number of offspring, on average.
4
¯
where F is the mean fecundity of all matings in the population.8
It probably won't surprise you to learn that it's very difficult to say anything very general
about how genotype frequenices will change when there's fertility selection. Not only are
there nine different fitness parameters to worry about, but since genotypes are never guar-
anteed to be in Hardy-Weinberg proportion, all of the algebra has to be done on a system
of three simultaneous equations.9 There are three weird properties that I'll mention:
¯ ¯
1. F may be smaller than F . Unlike selection on viabilities in which fitness evolved to
the maximum possible value, there are situations in which fitness will evolve to the
minimum possible value when there's selection on fertilities.10
2. A high fertility of heterozygote × heterozygote matings is not sufficient to guarantee
that the population will remain polymorphic.
3. Selection may prevent loss of either allele, but there may be no stable equilibria.
Conditions for protected polymorphism
There is one case in which it's fairly easy to understand the consequences of selection, and
that's when one of the two alleles is very rare. Suppose, for example, that A1 is very rare,
then a little algebraic trickery11 shows that
x11 0
x12 (F12,22 + F22,12 )/2
x12
F22,22
So A1 will become more frequent if
(F12,22 + F22,12 )/2 > F22,22 (2)
Similarly, A2 will become more frequent when it's very rare when
(F11,12 + F12,11 )/2 > F11,11 . (3)
If both equation (2) and (3) are satisfied, natural selection will tend to prevent either allele
from being eliminated. We have what's known as a protected polymorphism.
8
As an exercise you might want to see if you can derive the corresponding equations for x12 and x22 .
9
And you thought that dealing with one was bad enough!
10
Fortunately, it takes rather weird fertility schemes to produce such a result.
11
The trickery isn't hard, just tedious. Justifying the trickery is a little more involved, but not too bad.
If you're interested, drop by my office and I'll show you.
5
Conditions (2) and (3) are fairly easy to interpret intuitively: There is a protected poly-
morphism if the average fecundity of matings involving a heterozygote and the "resident"
homozygote exceeds that of matings of the resident homozygote with itself.12
NOTE: It's entirely possible for neither inequality to be satisfied and for their to be
a stable polymorphism. In other words, depending on where a population starts selection
may eliminate one allele or the other or keep both segregating in the population in a stable
polymorphism.
Sexual selection
A classic example of sexual selection is the peacock's tail. The long, elaborate tail feathers
do nothing to promote survival of male peacocks, but they are very important in determining
which males attract mates and which don't. If you'll recall, when we originally derived the
Hardy-Weinberg principle we said that the matings occurred randomly. Sexual selection is
clearly an instance of non-random mating. Let's go back to our original mating table and
see how we need to modify it to accomodate sexual selection.
Offsrping genotype
Mating Frequency A1 A1 A1 A2 A2 A2
A1 A1 × A1 A1 xf xm
11 11 1 0 0
A1 A2 xf xm
11 12
1
2
1
2
0
A2 A2 xf xm
11 22 0 1 0
A1 A2 × A1 A1 xf xm
12 11
1
2
1
2
0
A1 A2 xf xm
12 12
1
4
1
2
1
4
A1 A2 x f xm
12 22 0 1
2
1
2
A2 A2 × A1 A1 xf xm
22 11 0 1 0
A1 A2 xf xm
22 12 0 1
2
1
2
A2 A2 x f xm
22 22 0 0 1
What I've done is to assume that there is random mating in the populations among those
individuals that are included in the mating pool. We'll assume that all females are mated so
that xf = xij .13 We'll let the relative attractiveness of the male genotypes be a11 , a12 , and
ij
12
A "resident" homozygote is the one of which the populations is almost entirely composed when all but
one allele is rare.
13
There's a reason for doing this called Bateman's principle that we can discuss, if you'd like.
6
a22 . Then it's not too hard to convince yourself that
x11 a11
xm =
11
a
¯
x12 a12
xm
12 =
a
¯
x22 a22
xm
22 = ,
a
¯
where a = x11 a11 + x12 a12 + x22 a22 . A little more algebra and you can see that
¯
x2 a11 + x11 x12 (a12 + a11 )/2 + x2 a12 /4
11 12
x11 = (4)
a
¯
And we could derive similar equations for x12 and x22 . Now you're not likely to remember
this, but equation (4) bears a striking resemblance to one you saw earlier, equation (1). In
fact, sexual selection is equivalent to a particular type of fertility selection, in terms of how
genotype frequencies will change from one generation to the next. Specifically, the fertility
matrix corresponding to sexual selection on a male trait is:
A1 A1 A1 A2 A2 A2
A1 A1 a11 a12 a22
A1 A2 a11 a12 a22
A2 A2 a11 a12 a22
There are, of course, a couple of other things that make sexual selection interesting.
First, traits that are sexually selected in males often come at a cost in viability, so there's
a tradeoff between survival and reproduction that can make the dynamics complicated and
interesting. Second, the evolution of a sexually selected trait involves two traits: the male
characteristic that is being selected and a female preference for that trait. In fact the two
tend to become associated so that the female preference evokes a sexually selected response
in males, which evokes a stronger preference in females, and so on and so on. This is a
process Fisher referred to as "runaway sexual selection."
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