Campbell Biology: Concepts & Connections (9th Edition)
9th Edition
ISBN: 9780134296012
Author: Martha R. Taylor, Eric J. Simon, Jean L. Dickey, Kelly A. Hogan, Jane B. Reece
Publisher: PEARSON
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Chapter 9, Problem 16TYK
In 1981, a stray black cat with unusual rounded, curled-back ears was adopted by a family in Lakewood, California. Suppose you owned the first curl cat and wanted to breed it to develop a true-breeding variety. Describe tests that would determine whether the curl gene is dominant or recessive and whether it is autosomal or sex-linked. Explain why you think your tests would be conclusive. Describe a test to determine that a cat is true-breeding.
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Using the pedigree chart attached:
Above is a pedigree for colorblindness. Based on the pedigree, is the disease dominant or recessive and is it sex-linked or autosomal? Why? Furthermore, what is the probability that 18 on this chart is affected but the condition, and what is the probability that 18 is a carrier? Why? Are the probability of being a carrier and an affected individual different? Why?
What are the genotypes of the mother and father in the pedigree below? The pedigree shows albinism (an autosomal recessive trait). The shaded shapes represent albino individuals.
a.
mother - homozygous dominant; father - homozygous dominant
b.
mother - heterozygous; father - homozygous recessive
c.
mother - homozygous recessive; father - heterozygous
d.
mother - heterozygous; father - heterozygous
e.
mother - homozygous dominant; father - homozygous recessive
Albinism is a recessive disorder where there is a lack of melanin. Andrea and her husband Claude both have normal skin pigmentation. Andrea’s mother has the albino phenotype, but her father and her brother do not (normal pigmentation). Claude’s parents are both normal, but he has a sister who has the condition (is albino). Answer the following questions
If Andrea and Claude are carriers for the albino allele, what is the probability that they have an albino child?
If Andrea and Claude have a second child, what is the probability this child be normal (non-albino)?
NOTE: Draw a punnet square or show your work.
Chapter 9 Solutions
Campbell Biology: Concepts & Connections (9th Edition)
Ch. 9 - Connecting the Concepts 1. Complete this concept...Ch. 9 - Whether an allele is dominant or recessive depends...Ch. 9 - Edward was found to be heterozygous (Ss) for...Ch. 9 - Two fruit flies with eyes of the usual red color...Ch. 9 - A man with type B blood and a woman who has type A...Ch. 9 - Tim and Jan both have freckles (see Module 9.9),...Ch. 9 - Both Tim and Jan (problem 6) have a widows peak...Ch. 9 - In rabbits, black hair depends on a dominant...Ch. 9 - A fruit fly with a gray body and red eyes...Ch. 9 - A series of matings shows that the recombination...
Ch. 9 - A couple are both phenotypically normal, but their...Ch. 9 - Why do more men than women have colorblindness?Ch. 9 - In fruit flies, the genes for wing shape and body...Ch. 9 - Adult height in humans is at least partially...Ch. 9 - Heather was surprised to discover she suffered...Ch. 9 - In 1981, a stray black cat with unusual rounded,...Ch. 9 - SCIENTIFIC THINKING The breakthrough that led...
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- The following pedigree shows the pattern of inheritance of red-green color blindness in a family. Females are shown as circles and males as squares; the squares or circles of individuals affected by the trait are filled in black. What is the chance that a son of the third-generation female indicated by the arrow will be color blind if the father is not color blind? If he is color blind?arrow_forwardCystic fibrosis is an autosomal disease that mainly affects the white population, and 1 in 20 whites are heterozygotes. Genetic testing can diagnose heterozygotes. Should a genetic screening program for cystic fibrosis be instituted? Should the federal government fund it? Should the program be voluntary or mandatory, and why?arrow_forwardIn humans, the genetic disease cystic fibrosis is caused by a recessive allele (a). The normal (healthy) allele is dominant (A). What is the genotype of someone who has cystic fibrosis? What are the two different genotypes that a healthy person could have? If two people were both heterozygous for the cystic fibrosis gene, what fraction of their children would be likely to have this disease? Hint: Draw a Punnett square to figure it out.arrow_forward
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- Geneticists are concerned about three different genetic conditions present within their family. Achondroplasia is an autosomal dominant genetic disorder that results in short-limbed dwarfism. (A = achondroplasia allele; a = average height allele). Red-Green Color blindness is an X-linked recessive genetic disorder (Xc = color blindness allele; XC = normal color vision allele). The 7-year-old son has an autosomal recessive form of deafness. (h = deafness allele; H = normal hearing allele.) All three family members were karyotyped, and additional genetic testing was performed to determine the chromosomal location of the genes being studied. The figures below show the karyotypes of the mother and father with respect to the chromosomes containing the three genes mentioned above. Question: The couple’s 7-year-old son has all three of these genetic conditions (achondroplasia, color blindness and deafness). Taking into consideration the genotypes of his parents, what is the complete…arrow_forwardAlbinism in humans is autosomal and fully recessive to normal color. A couple, who are both normal, have a daughter who is albino and a son who is normal. What is the probability that their normal son is a carrier of the albinism gene?arrow_forwardA blue-eyed man, whose parents were brown-eyed, marries a brown-eyed woman whose father was blue-eyed and whose mother was brown-eyed. This man and woman have a blue-eyed child. What are the genotypes of all the individuals mentioned? (Brown is due to an autosomal dominant allele)arrow_forward
- For a recessive condition, two normal heterozygous individuals have children. What is the likelihood of their children being affected by this condition? What is the likelihood of their children being carriers without the condition? What is the likelihood of their asymptomatic children being carriers? Suppose that an individual with the condition has children with a heterozygous individual, what is the likelihood of their children being carriers?arrow_forwardA couple who are about to get married learn from studying their family histories that, in both their families, theirunaffected grandparents had siblings with cystic fibrosis(a rare autosomal recessive disease).a. If the couple marries and has a child, what is theprobability that the child will have cystic fibrosis?b. If they have four children, what is the chance that thechildren will have the precise Mendelian ratio of 3:1 fornormal:cystic fibrosis?c. If their first child has cystic fibrosis, what is theprobability that their next three children will be normal?arrow_forwardIn some breeds of dogs, a dominant allele controls the characteristics of barking while trailing. In these dogs, another independent allele produces erect ears; it is dominant over the allele for drooping ears. Suppose a dog breeder wants to produce a pure-breeding strain of droop-eared barkers, but he knows that the genes for silent trailing and erect ears are present in his kennels, how would he proceed?arrow_forward
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