In Exercises 21-28, find the probability and answer the questions.
X-Linked Genetic Disease Men have XY (or YX) chromosomes and women have XX chromosomes. X-linked recessive genetic diseases (such as juvenile retinoschisis) occur when there is a defective X chromosome that occurs without a paired X chromosome that is not defective. In the following, represent a defective X chromosome with lowercase x, so a child with the xY or Yx pair of chromosomes will have the disease and a child with XX or XY or YX or xX or Xx will not have the disease. Each parent contributes one of the chromosomes to the child.
a. If a father has the defective x chromosome and the mother has good XX chromosomes, what is the probability that a son will inherit the disease?
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Step 1: Understand the genetic inheritance. Each parent contributes one chromosome to the child. The father contributes either an X or a Y chromosome, while the mother contributes one of her two X chromosomes.
Step 2: Identify the genetic makeup of the parents. The father has a defective x chromosome (xY), and the mother has two good X chromosomes (XX).
Step 3: Determine the possible combinations of chromosomes for a son. A son inherits the Y chromosome from the father and one of the X chromosomes from the mother. The possible combinations are YX and Yx.
Step 4: Analyze the combinations. A son with the YX combination will not have the disease because the X chromosome from the mother is not defective. A son with the Yx combination will have the disease because the X chromosome from the mother is defective.
Step 5: Calculate the probability. Since the mother has two X chromosomes and each is equally likely to be passed on, the probability of the son inheriting the defective x chromosome is 1/2. Therefore, the probability that the son will inherit the disease is 1/2.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
X-Linked Inheritance
X-linked inheritance refers to the pattern of genetic transmission of traits or diseases that are associated with genes located on the X chromosome. In this case, males (XY) are more likely to express X-linked recessive diseases because they have only one X chromosome. If that X chromosome carries a defective gene, they will exhibit the disease, while females (XX) can be carriers if they have one defective X and one normal X.
Probability in genetics involves calculating the likelihood of inheriting specific traits based on the genetic makeup of the parents. In this scenario, the probability of a son inheriting the disease can be determined by analyzing the combinations of chromosomes contributed by each parent. The father's defective X chromosome and the mother's normal X chromosomes create a specific set of possible outcomes for their offspring.
A Punnett square is a diagram used to predict the genetic outcomes of a cross between two parents. It helps visualize the possible combinations of alleles that offspring may inherit. In this case, a Punnett square can be used to illustrate the potential genetic combinations of the father with the defective X chromosome and the mother with two normal X chromosomes, allowing for a clear calculation of the probability of the son inheriting the disease.