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Ch. 2 - Transmission Genetics
Sanders - Genetic Analysis: An Integrated Approach 3rd Edition
Sanders3rd EditionGenetic Analysis: An Integrated ApproachISBN: 9780135564172Not the one you use?Change textbook
Chapter 2, Problem 37c

Galactosemia is an autosomal recessive disorder caused by the inability to metabolize galactose, a component of the lactose found in mammalian milk. Galactosemia can be partially managed by eliminating dietary intake of lactose and galactose. Amanda is healthy, as are her parents, but her brother Alonzo has galactosemia. Brice has a similar family history. He and his parents are healthy, but his sister Brianna has galactosemia. Amanda and Brice are planning a family and seek genetic counseling. Based on the information provided, complete the following activities and answer the questions.


What is the probability that the first child of Amanda and Brice will have galactosemia? Show your work.

Verified step by step guidance
1
Step 1: Understand the inheritance pattern of galactosemia. It is an autosomal recessive disorder, meaning that an individual must inherit two copies of the defective allele (one from each parent) to express the condition. Carriers (heterozygous individuals) have one normal allele and one defective allele but do not show symptoms.
Step 2: Determine the genotypes of Amanda and Brice based on their family histories. Since Amanda and Brice are healthy but each has a sibling with galactosemia, their parents must be carriers (heterozygous). This means Amanda and Brice each have a 2/3 chance of being carriers (heterozygous) and a 1/3 chance of being homozygous for the normal allele.
Step 3: Calculate the probability that Amanda and Brice are both carriers. Multiply the probabilities: (2/3 for Amanda being a carrier) × (2/3 for Brice being a carrier).
Step 4: If both Amanda and Brice are carriers, calculate the probability of their child inheriting galactosemia. For two carrier parents, there is a 1/4 chance that their child will inherit two defective alleles and have galactosemia.
Step 5: Combine the probabilities from Step 3 and Step 4 to find the overall probability that Amanda and Brice's first child will have galactosemia. Multiply the probability of both being carriers by the probability of their child inheriting two defective alleles.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Autosomal Recessive Inheritance

Autosomal recessive inheritance occurs when a disorder is caused by mutations in genes located on the autosomes, and two copies of the mutated gene (one from each parent) are necessary for the individual to express the disorder. In the case of galactosemia, both parents must be carriers of the mutated gene for their child to have a chance of being affected. If both parents are carriers, there is a 25% probability that their child will inherit both mutated genes and express the disorder.
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Carrier Status

A carrier is an individual who has one copy of a mutated gene and one normal gene for a recessive disorder. Carriers do not exhibit symptoms of the disorder but can pass the mutated gene to their offspring. In the scenario, Amanda and Brice are likely carriers since their siblings have galactosemia, which informs the probability calculations for their potential children.
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Punnett Square

A Punnett square is a diagram used to predict the genetic outcomes of a cross between two individuals. It helps visualize the possible combinations of alleles from the parents. For Amanda and Brice, both being carriers (genotype Aa), a Punnett square can be used to determine the probabilities of their offspring being affected by galactosemia (aa), carriers (Aa), or unaffected (AA), providing a clear method to calculate the likelihood of their first child having the disorder.
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Related Practice
Textbook Question

You have four guinea pigs for a genetic study. One male and one female are from a strain that is pure-breeding for short brown fur. A second male and female are from a strain that is pure-breeding for long white fur. You are asked to perform two different experiments to test the proposal that short fur is dominant to long fur and that brown is dominant to white. You may use any of the four original pure-breeding guinea pigs or any of their offspring in experimental matings. Design two different experiments (crossing different animals and using different combinations of phenotypes) to test the dominance relationships of alleles for fur length and color, and make predictions for each cross based on the proposed relationships. Anticipate that the litter size will be 12 for each mating and that female guinea pigs can produce three litters in their lifetime.

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Textbook Question

Galactosemia is an autosomal recessive disorder caused by the inability to metabolize galactose, a component of the lactose found in mammalian milk. Galactosemia can be partially managed by eliminating dietary intake of lactose and galactose. Amanda is healthy, as are her parents, but her brother Alonzo has galactosemia. Brice has a similar family history. He and his parents are healthy, but his sister Brianna has galactosemia. Amanda and Brice are planning a family and seek genetic counseling. Based on the information provided, complete the following activities and answer the questions.

Draw a pedigree that includes Amanda, Brice, and their siblings and parents. Identify the genotype of each person, using G and g to represent the dominant and recessive alleles, respectively.

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Textbook Question

Galactosemia is an autosomal recessive disorder caused by the inability to metabolize galactose, a component of the lactose found in mammalian milk. Galactosemia can be partially managed by eliminating dietary intake of lactose and galactose. Amanda is healthy, as are her parents, but her brother Alonzo has galactosemia. Brice has a similar family history. He and his parents are healthy, but his sister Brianna has galactosemia. Amanda and Brice are planning a family and seek genetic counseling. Based on the information provided, complete the following activities and answer the questions.


What is the probability that Amanda is a carrier of the allele for galactosemia? What is the probability that Brice is a carrier? Explain your reasoning for each answer.

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Textbook Question

Galactosemia is an autosomal recessive disorder caused by the inability to metabolize galactose, a component of the lactose found in mammalian milk. Galactosemia can be partially managed by eliminating dietary intake of lactose and galactose. Amanda is healthy, as are her parents, but her brother Alonzo has galactosemia. Brice has a similar family history. He and his parents are healthy, but his sister Brianna has galactosemia. Amanda and Brice are planning a family and seek genetic counseling. Based on the information provided, complete the following activities and answer the questions.


If the first child has galactosemia, what is the probability that the second child will have galactosemia? Explain the reasoning for your answer.

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Textbook Question

Sweet yellow tomatoes with a pear shape bring a high price per basket to growers. Pear shape, yellow color, and terminal flower position are recessive traits produced by alleles f, r, and t, respectively. The dominant phenotypes for each trait—full shape, red color, and axial flower position—are the product of dominant alleles F, R, and T. A farmer has two pure-breeding tomato lines. One is full, yellow, terminal and the other is pear, red, axial. Design a breeding experiment that will produce a line of tomato that is pure-breeding for pear shape, yellow color, and axial flower position.

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Textbook Question

A cross between a spicy variety of Capsicum annum pepper and a sweet (nonspicy) variety produces F1 progeny plants that all have spicy peppers. The F1 are crossed, and among the F2 plants are 56 that produce spicy peppers and 20 that produce sweet peppers. Dr. Ara B. Dopsis, an expert on pepper plants, discovers a gene he designates Pun1 that he believes is responsible for spicy versus sweet flavor of peppers. Dr. Dopsis proposes that a dominant allele P produces spicy peppers and that a recessive mutant allele p results in sweet peppers.

Are the data on the parental cross and the F1 and F2 consistent with the proposal made by Dr. Dopsis? Explain why or why not, using P and p to indicate probable genotypes of pepper plants.

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