Some genes that cause genetic diseases interact in a dominant-recessive pattern. In these cases, two copies of the recessive gene are required for the disease to occur. A person who has just one copy of the recessive gene is termed a carrier, since he or she carries the gene but is not affected by it. In the illustration above, the dominant gene is represented in green, and the recessive in blue. For the couple on the left, the father has one copy of the dominant gene and one copy of the recessive gene. The mother has two copies of the dominant gene. Each parent can contribute just one gene to the child. The four children shown on the lower left represent the probabilities (not the actual children) for the combinations that can result from their parents. The children on the far left received the recessive gene from their father and the dominant gene from their mother, and are therefore carriers. For any child born to these parents, there is a 50 percent chance that the child will be a carrier. Since none of the children can inherit two copies of the recessive gene, none of the children will develop the disease. When both parents are carriers, however, as shown by the couple on the right, there is a 25 percent chance that any child born has the disease, a 50 percent chance that a child is a carrier, and a 25 percent chance that a child does not have the disease and is not a carrier.
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