Gene Segregation After a Cross
What Happens to the Heterozygous Gene Pairs?
Now
let's look
what happens to the genes of the F1 hybrid population when allowed to
self pollinate.
note- the ability for a tomato to
self pollinate is critical. It prevents any other genes from being
introduced and this sets up how it is that true-breeding lines can be
maintained or created.
Now that each
gene pair is heterozygous in the F1, when the reproductive cells
reduce, they have an equal chance of
contributing either a dominate or recessive gene. As these halves
recombine to make
a new "egg" pair, one now gets all three types of gene outcomes
and
again both
leaf types appear in the new F2 generation's population. The gene
outcome is
called genotype and the leaf appearance is called the phenotype.
- genotype - what the genes are
- phenotype - how they look
X
|
ovule
|
ovule
|
pollen
|
heterozygous
|
homozygous
dominate
|
pollen
|
homozygous
recessive
|
heterozygous
|
| genotypic
ratio |
1:2:1 |
1
dominate : 2 heterozygotes : 1 recessive
25% dominate | 50% heterozygous | 25% recessive
|
| phenotypic
ratio |
3:1 |
3
regular leaf plants for each potato leaf plant |
how
many are still heterozygous?
|
50%
heterozygous
50% homozygous |
The
amount of heterozygotes was reduced by half
|
The
new generation is called the "F2". Notice that the amount
of "unlike genes" (heterozygotes) are reduce to half of the total
population compared to the F1 generation. Notice also that the
population's phenotype (how it looks) is about 75%
regular leaves and 25% potato leafed or a 3:1 ratio.
Of the regular
leafs, one still can't tell exactly which offspring are
homozygous dominate and which are
heterozygous (what their genotype is) but by the probability
table
above one knows that the chance is that most of the regular leaf types
will
be heterozygous and less than half of the regular leaf types will be
completely homozygous.
In the previous
page I stated that over time inbreeding populations, like that of
tomato, want to become completely homozygous. Let's look at how that
happens below. I don't have that
many eggs so I need to switch to other symbols to represent the eggs.
Let's start back
with the F1 hybrid generation. Allow the F1 hybrid to self pollinate to
create a new F2 generation. Randomly select 128 seeds to grow out the
F2 population and see what happens. Then allow that F2 generation to
self
pollinate and randomly
select
another 128 seeds to grow out to create an F3 generation and so on for
7 generations.
Each
generation is created by allowing the plants to only self pollinate and
then
randomly selecting 128 seeds
it produces.
note - I only choose the number 128
because it works well to make the charts below
Look
what
happens to the unlike paired genes over time in randomly selected
populations.
F1
100%
|
|
F2
50%
|
|
F3
25%
|
|
|
|
|
|
F4
12.5%
|
|
F5
6.25%
|
|
F6
3.125%
|
|
|
|
|
|
|
|
|
|
|
F7
1.6%
|
F8
0%
|
|
|
|
|
After selfing,
each subsequent generation reduces the amount of "unlike genes" in half
until
they are virtually all removed. Once the chance of unlike genes
is
gone, the populations will be all
homozygotes.
Now what I have
shown you is the mathematical or statistically probability. In "real
life" one is not likely to see such "exact numbers".
For the example
above the F2 produced 96 regular leaf types to 32 potato leaf types or
a 3:1 ratio. In real life, because one randomly chooses, that actual
number may be different but fairly close to the 3:1 ratio (ie you might
see something like 108:20). Genetists use a test called a Chi-square
test to determine if what one "sees" actually fits what one
"expects".
If it "fits" the test that means the inheritance is simple and as
expected. If it doesn't "fit" the test that might indicate some other
method of inheritance is going and further tests might be needed to
determine what is going on genetically with that trait. This test is not normally necessary for amateur
breeders especially when one can determine the inheritance of a given
trait ahead of time (like we know about regular vs potato leafed).
Another point to
make about segregation is that in a population, especially very large
ones, the heterozygotes don't necessarily completely disappear. This is why I
said above "virtually all gone" on the previous page
concerning true breeding homozygous populations. Even in a controlled population with
NO outcrossing or no random mutations, there is a chance that some "unlike genes" are still
left in the population due to random assortment (real life number as
opposed to theoretical probabilities). Let me use the table
below totry and illustrate this point:
Again notice how
in each generation the number of the "unlike genes" is reduced in
half from the generation before..
Generation
|
heterozygotes
|
homozygotes
|
F1
|
100%
|
0%
|
F2
|
50%
|
50%
|
F3
|
25%
|
75%
|
F4
|
12.5%
|
87.5%
|
F5
|
6.3%
|
93.7%
|
F6
|
3.1%
|
96.8%
|
F7
|
1.6%
|
98.4%
|
F8
|
0.8%
|
99.2%
|
F9
|
0.4%
|
99.6%
|
F10
|
0.2%
|
99.8%
|
F11
|
0.1%
|
99.9%
|
F12
|
0.05%
|
99.95%
|
F13
|
0.025%
|
99.975%
|
F14
|
0.0125%
|
99.9875%
|
But notice also
from this table that when one keeps taking half of something, they
never conclusively reach "zero". In the "egg chart", for all practical purposes "zero"
is pretty much reached by the F8. But because of random assortment, there is a small chance that some
unlike genes are left over in the population. This is even more
pronounced in larger populations.
Example: In an F12
population of 10,000 seeds there is a 0.05% chance of unlike gene pairs.
(0.05%/100
= 0.0005) 10,000 x 0.005 = 5 plants which will
be heterozygous
This is another
reason why it is important that one carry out line development of
creating a new line or de-hybridizing to at least the F7 before
releasing or naming.
So it ends up
being a numbers game. The result is that even generally stable
populations of true-breeding individuals sometimes can potentially
contain
off-types by random chance and this must be considered. Fortunately for
amateur tomato breeders large populations
are not practical and chances are if you have taken the population out
to an F7 or F8 you a good chance of completely removing these - but
there still is some chance.
The main points to this page are:
- tomato
genes want to revert back to being homozygous by sorting independently
- to become
relatively stable and true-breeding, lines should be carried out to the
F7 or F8 generation and
- that there
still exists a small chance that some heterzygotes (off-types) can be
in an advanced population.
Let us
now look at how we can use the segregation above to produce new and
stable varieties.
NEXT