Evolution occurs through a history of genetic recombination
and natural selection. Genetic recombination creates the variability
found within a population, and selection inbreeds the chosen
characteristics creating a "pure-breed". Following
a history of selection the organism has limited genetic variability,
and its offspring are virtually identical. That is what you pay
for when you buy a registered animal or plant seed-line. You
are buying a guarantee that the traits, which have been selected,
will not segregate out in subsequent generations. The animal
registration is verification that its genotype is free from related
variability, and the offspring from its lineage will possess
a known phenotype for the characteristics in question.
A pure-breed is a genetic homozygote, or
an individual which no longer possesses alternative variations
for the genes in question. Most genes are present as a number
of varieties (alleles) and as a result the traits they produce
are polymorphic or present in more than one form. The homozygote
will no longer produce variable offspring because the genome
can no longer pass a variety of genes to its daughter cells.
Selection for any specific characteristic is "outselection"
of the alternative alleles from the population. Natural selection,
in this respect, works in the exact same way as artificial breeding.
Selection removes genes from the population, and eventually eliminates
the organisms ability to produce progeny that differ. Following
a period of selection, the organisms ability to produce a variability
is frequently lost forever.
Prior to selection, an organism will typically
be heterozygote or have different copies of the gene at the same
loci. A genetic homozygote can be generated for any characteristic.
Simply mate two organisms possessing the desired trait, and one
of their children will likely be pure-bred for a related gene.
The test for homozygosity is rather simple. Basically; if every
child possess a trait, the parent is a homozygote and from that
organism a pure blood-line begins. Alternatively look for a family
whose entire progeny possess a trait, and at least one of their
parents is homozygote.
If both parents are heterozygote,
or each has only one copy of the allele in question, then it
is expected for 25% of their offspring to be homozygote.
(AA, Aa, aA, aa). 25% - aa
Parental Genotypes
Heterozygotes
(Aa) + (Aa) |
A |
a |
|
A |
AA |
Aa |
|
a |
aA |
aa |
If you subsequently select the
homozygote and mate it with another heterozygote; 75% of the
offspring will be homozygote. This is how selection rapidly transforms
a poplulation.
(Aa, aa, aa, aa). 75% - aa
Parental Genotypes
Heterozygotes /Homozygote
(Aa) + (aa) |
a |
a |
|
A |
Aa |
aa |
|
a |
aa |
aa |
Animals evolve because nature selects from
a pool of alleles, and the resulting homozygotes are genetically
pure bred for the features which gave the organisms the specific
adaptation. Although few characteristics are simplified to a
single pair of alleles, it is clear that selection (inbreeding
selected features) will generate and then multiply genetic homozygotes
for the related genes within the population. If selection persists,
these homozygotes will rapidly become predominant, and the group
as a whole will become more limited genetically as a result of
the selection. The reduction of alleles or heterozygosity from
inbreeding has been shown to contribute to the decline, and eventual
extinction of isolated population. (1)
The
galapagos finch varieties are the result of genetic recombination
just like all the domestic breeds, and now just exist as several
naturally pure-bred species. Evolution occur because nature chooses
(inbreeds) particulars characteristics from existing variability,
and following a period of selective breeding the entire population
becomes homozygous. They are more fit for the specific conditions
they were selected to, but less able to change as a result.
Although it would appear that evolution
through meiotic recombination or classic mendelian genetics is
largely a one-way street, we must remember that the wolf was
a homozygote in nature. The wolf is part of a larger group, which
also includes the hyena, jackal, fox, coyote, and others. The
wolf was selected, along with these other natural canines, until
it was a pure bred or genetic homozygote and would only produce
wolf pups. The variety of breeds that was later isolated from
the wolf lineage appears to have accumulated gradually because
we eliminated the natural selection which previously kept the
genome pure of this variability.
Contrary to popular opinions among creationists,
this indicates an ability to produce continued variability following
homozygosity. We were able to isolate the domestic breeds from
the wolf, but apparently not because of alleles that were already
present. The wolf was a pure breed, and it is likely that continued
diversity among such purebred organisms is generated through
cellular mechanisms known as homologous
recombination. It is now certain that some genes are variable,
and others are not. Genes that are involved with direct inter-species
contact, such as toxins, are found highly variable among closely
related species. In contrast, housekeeping genes are found conserved
among vastly different organisms.
The tremendous diversity found isolated
by domestic breeding may therefore be the result of variable
genes or new alleles that have been generated by cellular mechanisms.
As these changes are also responsible for environmental adaptation,
the very basis of evolution is clearly the result of cellular
intent instead of mutations. Given our knowledge of genetic
recombination, the cell's ability to edit the genome is theoretically
limitless.
by Chris W. Ashcraft
References
Quotes
(1) Dessauer, H. C., G.
F. Gee, and J. S. Rogers. 1992. Allozyme evidence for crane systematics
and polymorphisms within populations of sandhill, sarus, Siberian
and whooping cranes. Molecular Phylogenetics and Evolution 1:279-288.
There are 15 living species of cranes, all of which were sampled
for this study. Based on protein electrophoresis, the two species
of African crowned cranes are distinct from the remaining species,
which are themselves divided into two groups. The "sandhill
group" consists of seven species, and is distributed across
the Old World, with the sandhill crane reaching North America.
The "whooper group" consists of six species which are
all restricted to the northern continents.
Single species diversity was also analyzed. A significant result
was the discovery that genetic diversity among whooping cranes
was surprisingly high, similar to that for the six other species
with which it was compared. This is contrary to expectations
of genetic loss due to a population bottleneck of some 15 individuals
in the 1940s. The possibility should be explored that some mechanism
exists for rapidly restoring genetic variability after population
bottlenecks.

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