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For understanding the inheritance of a trait where only one pair of genes is involved,<br />
following facts (laws) can be stated (I) genes occur in pairs in the body cells of the individual,<br />
(2) one of each pair came from the father and one from the mother, (3) the genes of a pair<br />
separate during formation of sex cells, and (4) on fertilization, the genes are restored to the<br />
paired condition.<br />
The law of chance determines which sperm and which egg will combine at the time of<br />
fertilization to form the new individual. The 1:2:1 genotypic ratio for the offspring of two<br />
heterozygous (Pp) inclividuals works well on paper, but under practical conditions the actual<br />
ratio may be far from the expected. Actually, when a small number of offspring are produced<br />
from such a mating, all might be of one genotype of either PP, Pp, or pp. The larger the number<br />
of offspring produced, the more likely it is that the expected ratio will occur. A similar<br />
condition is observed in the number of boys and girls that may occur in any one family. The<br />
chances of any one baby being a boy is one out of two, for it has an equal chance of being a boy<br />
or girl. Yet, many of us have seen even large families where all the children are of the same<br />
sex. This happens because of the law of chance.<br />
Six different kinds of matings, with reference to parental genotype, are possible when one<br />
pair of genes is involved and where dominance is complete. These are listed as under:<br />
Genotypic of Genotypic ratio Breeding ability of<br />
Parents of offspring offspring<br />
PPxPp { IPP Breedstrue<br />
{ 1 Pp Doesn't breed true<br />
PP x PP All PP All breed true<br />
PP x pp All Pp None breed true<br />
Pp x Pp {I PP Breeds true<br />
{2 Pp None breed true<br />
{ I pp Breeds true<br />
Pp x pp { I Pp None breed true<br />
{ Ipp All breed true<br />
pp x pp All pp All breed true<br />
5.5.2 Incomplete Dominance - Coat colour<br />
Occasionally, modifications of this simple two-gene inheritance, are observed. For<br />
example, the case of coat color in sheep. Three different coat colors appear in the sheep having<br />
red coat colour: redgRR), roan (RW), and white (WW). When a roaan ram (RW) is mated to a<br />
group of raon ewes (RW), the offspring will be colored in the ratio of one red (RR) to two roan<br />
(RW) to one white (WW). It should be noted that this is the same genotypic ratio that is<br />
obtained when dominance is complete, and as, in the example where polled was dominant to<br />
horned. But in this instance, the heterozygote expresses itself phenotypically in a different<br />
manner from either homozygote, and the genotypic and phenotypic ratios are the same, 1:2:1.<br />
This type of gene action is called incomplete dominance, or a blending type of inheritance. One<br />
practical point here is that, even though it is not possible to develop a pure breeding roan herd<br />
(RW), because the roan individuals are all heterozygous a d will not breed true, it is always<br />
possible to produce roan sheep (RW) by mating a red parent (RR) to a white parent (WW).<br />
Many cases of inheritance are known where dominance is incomplete and the genotypic<br />
and phenotypic ratios of the offspring of a mating between heterozygous parents are the same.<br />
For exarnple, palomino horses will not breed true, because they are heterozygous for genes for<br />
color, but they can always be produced by mating chestnut sorrels with pseudo albinos.<br />
Another example is in Comprest Herefords, which are heterozygous for the comprest gene.<br />
When mated, comprests produce offspring in the ratio of 1 normal (cc) to two comprest (Cc) to<br />
one dwarf (CC). Of course, in this instance it is impossible to mate the normals (cc) with the<br />
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