Contributed by Vic High:
I've been hearing a fair bit of
confusion from many on how to create
a true breeding strain and so I'm
writing this page to try and help
shed some light on the subject.
There are a few situations where a
plant breeder would want to create a
true breeding strain (IBL) and a few
ways of accomplishing the task. But
understanding the subtle differences
of the various techniques is not so
easy. This paper will attempt to
give a basic understanding of what
is actually happening with each
technique and then apply what is
learned to actual projetcs. As a
friend worked overtime making sure I
didn't forget, breeding is not a
black and white subject and as a
whole, it would be too complex to
put on paper in an easily understood
form. Therefore, I will create small
fictional examples to reinforce
various concepts and then we will
take those examples and concepts and
apply some reality to them. Try not
to get hung up on the erroneous
assumptions used here such as
flavour being monogenic, the
assumption is simply used to make it
easier to learn a certain concept.
Just What Is It That We Are
Doing?
Before we dive in, maybe we should
take the time to understand what we
are trying to accomplish when we set
out to create a true breeding
strain. There are hundreds of
possible phenotypic traits that we
could observe within a cannabis
population. Are we trying to make
all of them the same and remove ALL
variation? Not likely, the genetic
code is just too complex to try.
Plus, since phenotype (what we see)
is 1/2 genotype + 1/2 environment,
everytime the population was grown
under new conditions, new
heterozygous traits would be
observed. Basically, all we are
trying to create is an overall
uniformity while not worrying about
the minor individual variations. No
different than a dog breed. You can
look at a german shepard and
recognise it as belonging to a
discrete breed. But if you look
closer at several german shepards
all at the same time, you will find
variations with each and every one
of them. Some will be a little
taller, some a little wider, some
more agressive, some a little
fatter, some darker, etc. But they
would all fall within an acceptable
range for the various traits.
Generally speaking, this is what a
plant breeder is trying to
accomplish when creating a true
breeding strain, or IBL.
However this isn't always the case.
Sometimes a breeder will just
concentrate on a specific trait,
like say outdoor harvest date, or
mite resistance. You could still
have a population where some are 2'
bushes and some 10' trees. In this
case, you would say that the strain
was true breeding for the particular
trait, but you wouldn't consider it
true breeding strain per se. In
genetics, wording plays a big part
in meaning and understanding. As
does point of reference as my F1 vs
F2 comparison page illustrates.
Ok, so we want to make a cannabis
population fairly uniform over a few
phenotypically important traits,
like say flavour for instance. For
simplicity sake, we'll just deal
with the single trait flavour, it's
complex enough. And although flavour
is controlled by several gene pairs
(polygenic), we'll make the
simplistic assumption that it's
controlled by a single gene pair
(monogenic) for many of the models
and examples in this paper. There
are many flavours such as chocolate,
vanilla, musky, skunky, blueberry,
etc, but in this paper we'll just
deal with two flavours, pine and
pineapple. Either gene in the gene
pair can code for either of the
flavours. If both genes code for
pineapple or both genes code for
pine flavour, we say that the gene
pair (and individual plant) is
homozygous for flavour. If the one
gene codes for pine and the other
codes for pineapple, we say that the
gene pair (and individual plant) is
heterozyous with respect to flavour.
The heterozygous individual can
create gametes (pollen or ovules)
that can code for either pine
flavour or pineapple flavour, the
homozygous individuals can only
create gametes that code for one OR
the other. A homozygous individual
is considered true breeding and a
heterozygous individual is not.
However, as the words imply, when we
are creating a true breeding strain,
we are looking at a population, not
individuals. We are trying to make
all the individuals in the
population homozygous for a
particular trait or group of traits.
Lets say we have a population of 50
individual plants, and each plant
has has a gene pair coding for
flavour. That means that 100 flavour
genes make up the flavour genepool
(reality is much more complex). When
trying to create a true breeding
strain, we are in fact trying to
make all 100 of those genes code for
the same trait ( pineapple flavour
in our case). The closer our
population comes getting all 100
genes the same, the more homozygous
or true breeding it becomes. We use
the terminology gene frequency to
measure and describe this concept,
where gene frequency is simply the
ratio or percentage of the
population that actually contains a
specific gene. The higher the gene
frequency, the more true breeding
the population is. A fixed trait is
where the gene frequency of the
trait reaches 100%.
And folks, this is the basic
backbone of what breeding is all
about, manipulating gene
frequencies. It doesn't matter if
your making IBL, F1s, F2s, selecting
for this or selecting for that, all
you are really doing is manipulating
gene frequencies. Therefore, to ever
really understand what is happening
in any breeding project, the breeder
must pay attention to gene
frequencies and assess how his
selective pressures and models are
influencing them. They are his
measure of success.
What are we trying to create a
true breeding strain from?
This a good question. Sometimes a
gardener will notice a sport or
unique individual in an F2
population, like say it has
pineapple flavour when the rest have
pine flavour. For one reason or
another he decides he wants to
preserve this new trait or
combination of traits from that
single individual. For the sake of
ease of comprehension, we tend to
call this special unique individual
the P1 mom. He could start by
selfing the individual OR breeding
that individual with another and
create what can be described as F1
offspring. If the F1 route was
chosen, then breeders can diverge
down two new paths. Some breeders
will take the progeny of the F1
crossing and breed it back to the P1
mom, and then repeat for a couple
more generations. This is referred
to as backcrossing or cubing by
cannabis breeders. Another common
strategy is to make F2 progeny from
the F1 population and then look for
individuals that match the P1 mom.
They would repeat the process for a
few generations. We can call this
filial or generational inbreeding
since the parents from each cross
belong to the same generation.
In another situation, sometimes a
farmer will notice a few individuals
in his fields that stand out from
the crowd in a possitive manner.
Like say the are resistant to a
problem pest like powdery mildew. In
this case, he will collect the best
of the individuals and his starting
population will contain several
similar individuals and not a unique
single individual as in the previous
example. He would skip the
hybridizing step (making the F1s)
and go straight to the generational
inbreeding step. Links to pages
going into detail of each of these
basic techniques and their impact on
influencing gene frequencies are at:
A)
Selfing the individual
B)
Backcrossing and Cubing
C) Filial or Generational Inbreeding
from an individual
D) Filial or Generational Inbreeding
from a group
Applying the Pressure
Another excellent method to
influence gene frequencies is to
apply selective pressure. The idea
here is to select only individuals
that carry the desireable genes, and
discard the rest.
A) Principles of selection
B)
Progeny tests