Campbell Biology
12th Edition
ISBN: 9780135188743
Author: Urry
Publisher: PEARSON
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Chapter 14, Problem 18TYU
SYNTHESIZE YOUR KNOWLEDGE
Just for fun, imagine that "shirt-striping" is a phenotypic character caused by a Single gene. Construct a genetic explanation for the appearance of the family in the above photograph, consistent with their "Shirt phenotypes." Include in your answer the presumed allele combinations for "shirt-striping" in each family member. Identify the inheritance pattern shown by the child.
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Just for fun, imagine that "shirt-striping" is a phenotypic
character caused by a single gene. Construct a genetic expla-
nation for the appearance of the family in the above pho-
tograph, consistent with their "shirt phenotypes." Include
in your answer the presumed allele combinations for "shirt-
striping" in each family member. Identify the inheritance
pattern shown by the child.
Suppose two parents, a father with the genotype AaBbccDd and a mother with the genotype aaBbCcDd, want to have children. Assume the loci are inherited independently of each other. Enter your answers as the most simplified fractions (e.g. 1/8 instead of 2/16). What proportion of the offspring are expected to have:
The same genotype as the father?
The same phenotype as the father?
All dominant phenotypes?
All recessive phenotypes?
Just for fun, imagine that “shirt-striping” is a phenotypic character caused by a single gene. Construct a genetic explanation for the appearance of the family in the above photograph, consistent with their “shirt phenotypes.” Include in your answer the presumed allele combinations for “shirt-striping” in each family member.
Chapter 14 Solutions
Campbell Biology
Ch. 14.1 - DRAW IT Pea plants heterozygous for flower...Ch. 14.1 - WHAT IF? List all gametes that could be made by a...Ch. 14.1 - MAKE CONNECTIONS In some pea plant crosses, the...Ch. 14.2 - Prob. 1CCCh. 14.2 - Two organisms, with genotypcs BbDD and BBDd, are...Ch. 14.2 - WHAT IF? Three characters (flower color, seed...Ch. 14.3 - What two properties, one structural and one...Ch. 14.3 - If a man with type AB blood marries a woman with...Ch. 14.3 - WHAT IF? A rooster with gray feathers and a hen...Ch. 14.4 - Prob. 1CC
Ch. 14.4 - Prob. 2CCCh. 14.4 - Prob. 3CCCh. 14.4 - MAKE CONNECTIONS In Table 14.1, note the...Ch. 14 - When Mendel did crosses of true-breeding purple-...Ch. 14 - DRAW IT Redraw the Punnett Square on The right...Ch. 14 - Inheritance patterns are often more complex than...Ch. 14 - Both members of a couple know that they are...Ch. 14 - Prob. 1TYUCh. 14 - A man with type A blood marries a woman with type...Ch. 14 - A man has six fingers on each hand and six toes on...Ch. 14 - Prob. 4TYUCh. 14 - Flower position, stem length, and seed shape are...Ch. 14 - Hemochromatosis is an inherited disease caused by...Ch. 14 - The genotype of F1, individuals in a tetrahybrid...Ch. 14 - What is the probability that each of thc following...Ch. 14 - Prob. 9TYUCh. 14 - Prob. 10TYUCh. 14 - In tigers, a recessive allele of a particular gene...Ch. 14 - In maize (com) plants,a dominant allele I inhibits...Ch. 14 - The pedigree belowtraces the inheritance of...Ch. 14 - Imagine that you are a genetic counselor, and a...Ch. 14 - EVOLUTION CONNECTION Over the past half century,...Ch. 14 - SCIENTIFIC INQUIRY You are handed a mystery pea...Ch. 14 - Prob. 17TYUCh. 14 - SYNTHESIZE YOUR KNOWLEDGE Just for fun, imagine...
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- The questions below all refer to the following pedigree. The locus for allele D/d determines how cilia function within the body. Mutations at this allele cause abnormal ciliary function, resulting in a clinical disorder characterized by frequent respiratory infections (including in the ears, sinuses, and lungs), as well as infertility. In the pedigree, black circles/squares represent individuals affected by the disorder. White circles/squares represent unaffected individuals. Remember, if a trait is rare in a population (such as this one), we assume individuals marrying into the family are NOT carriers unless the information provided indicates otherwise. A1 A2. || B1. B2. B3 B4. B5 B6. II C1_ C2. C3. C4. C5 IV D1 D2- D4 - D5_ 1) What is the probability that B3 is a carrier of this disorder? Show your work with a Punnett Square in addition to stating the probabilityarrow_forwardThe questions below all refer to the following pedigree. The locus for allele D/d determines how cilia function within the body. Mutations at this allele cause abnormal ciliary function, resulting in a clinical disorder characterized by frequent respiratory infections (including in the ears, sinuses, and lungs), as well as infertility. In the pedigree, black circles/squares represent individuals affected by the disorder. White circles/squares represent unaffected individuals. Remember, if a trait is rare in a population (such as this one), we assume individuals marrying into the family are NOT carriers unless the information provided indicates otherwise. ||| IV B1 C1_ B2 C2 D1 A1 C3 D2 Probability that D5 is a carrier: B3 A2 B4 Probability that Taylor is a carrier: org B5 O C4. D4____ Probability that two carriers will have an affected child: C5 1) What is the probability that B3 is a carrier of this disorder? Show your work with a Punnett Square in addition to stating the probability…arrow_forwardA student is completing a Punnett square for a trait (X/x) that is autosomal and inherited by the dominant allele. The father does not have it (xx), but the mother does (Xx). If they had two children, a son and a daughter, what would the completed Punnett square look like (i.e., would the son have the trait, would the daughter have the trait)? Both children would inherit the trait. Both children would not inherit the trait. Each child has a 50% chance of inheriting the trait. One child would inherit the trait and one child would not.arrow_forward
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- Pedigree analysis is a fundamental tool for investigating whether or not a trait is following a Mendelian pattern of inheritance. It can also be used to help identify individuals within a family who may be at risk for the trait. Adam and Sarah, a young couple of Eastern European Jewish ancestry, went to a genetic counselor because they were planning a family and wanted to know what their chances were for having a child with a genetic condition. The genetic counselor took a detailed family history from both of them and discovered several traits in their respective families. Sarahs maternal family history is suggestive of an autosomal dominant pattern of cancer predisposition to breast and ovarian cancer because of the young ages at which her mother and grandmother were diagnosed with their cancers. If a mutant allele that predisposed to breast and ovarian cancer was inherited in Sarahs family, she, her sister, and any of her own future children could be at risk for inheriting this mutation. The counselor told her that genetic testing is available that may help determine if this mutant allele is present in her family members. Adams paternal family history has a very strong pattern of early onset heart disease. An autosomal dominant condition known as familial hypercholesterolemia may be responsible for the large number of deaths from heart disease. As with hereditary breast and ovarian cancer, genetic testing is available to see if Adam carries the mutant allele. Testing will give the couple more information about the chances that their children could inherit this mutation. Adam had a first cousin who died from Tay-Sachs disease (TSD), a fatal autosomal recessive condition most commonly found in people of Eastern European Jewish descent. Because TSD is a recessively inherited disorder, both of his cousins parents must have been heterozygous carriers of the mutant allele. If that is the case, Adams father could be a carrier as well. If Adams father carries the mutant TSD allele, it is possible that Adam inherited this mutation. Because Sarah is also of Eastern European Jewish ancestry, she could also be a carrier of the gene, even though no one in her family has been affected with TSD. If Adam and Sarah are both carriers, each of their children would have a 25% chance of being afflicted with TSD. A simple blood test performed on both Sarah and Adam could determine whether they are carriers of this mutation. Would you want to know the results of the cancer, heart disease, and TSD tests if you were Sarah and Adam? Is it their responsibility as potential parents to gather this type of information before they decide to have a child?arrow_forwardPedigree analysis is a fundamental tool for investigating whether or not a trait is following a Mendelian pattern of inheritance. It can also be used to help identify individuals within a family who may be at risk for the trait. Adam and Sarah, a young couple of Eastern European Jewish ancestry, went to a genetic counselor because they were planning a family and wanted to know what their chances were for having a child with a genetic condition. The genetic counselor took a detailed family history from both of them and discovered several traits in their respective families. Sarahs maternal family history is suggestive of an autosomal dominant pattern of cancer predisposition to breast and ovarian cancer because of the young ages at which her mother and grandmother were diagnosed with their cancers. If a mutant allele that predisposed to breast and ovarian cancer was inherited in Sarahs family, she, her sister, and any of her own future children could be at risk for inheriting this mutation. The counselor told her that genetic testing is available that may help determine if this mutant allele is present in her family members. Adams paternal family history has a very strong pattern of early onset heart disease. An autosomal dominant condition known as familial hypercholesterolemia may be responsible for the large number of deaths from heart disease. As with hereditary breast and ovarian cancer, genetic testing is available to see if Adam carries the mutant allele. Testing will give the couple more information about the chances that their children could inherit this mutation. Adam had a first cousin who died from Tay-Sachs disease (TSD), a fatal autosomal recessive condition most commonly found in people of Eastern European Jewish descent. Because TSD is a recessively inherited disorder, both of his cousins parents must have been heterozygous carriers of the mutant allele. If that is the case, Adams father could be a carrier as well. If Adams father carries the mutant TSD allele, it is possible that Adam inherited this mutation. Because Sarah is also of Eastern European Jewish ancestry, she could also be a carrier of the gene, even though no one in her family has been affected with TSD. If Adam and Sarah are both carriers, each of their children would have a 25% chance of being afflicted with TSD. A simple blood test performed on both Sarah and Adam could determine whether they are carriers of this mutation. If Sarah carries the mutant cancer allele and Adam carries the mutant heart disease allele, what is the chance that they would have a child who is free of both diseases? Are these good odds?arrow_forwardConsider the Mendelian inherited genes below (complete dominance.) Draw your answer on paper and upload a photo here or complete your answer digitally and upload your file in a common format here. A. Track one gene: Blue bonnet flower color. Dominant allele = blue flowers, B; Recessive allele = white flowers, b Cross: heterozygous plant x homozygous recessive plant Set up and draw the Punnett square for this cross Predict % likelihood of offspring possible genotype & phenotypes B. Track two genes: Bluebonnet flower color and plant height Flower color: blue dominant B, white recessive b Plant height: tall dominant T, short recessive t Cross: heterozygous plant x homozygous recessive plant Set up and draw Punnett square Predict % likelihood of offspring genotypes and phenotypesarrow_forward
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