In tomatoes, red fruit is dominant over yellow, two-loculed fruit is dominant over many-loculed fruit, and tallvine is dominant over dwarf. A breeder has two purelines: (1) red, two-loculed, dwarf and (2) yellow, manyloculed, tall. From these two lines, he wants to produce anew pure line for trade that is yellow, two-loculed, andtall. How exactly should he go about doing so? Show notonly which crosses to make, but also how many progenyshould be sampled in each case.

In tomatoes, red fruit is dominant over yellow, two-loculed fruit is dominant over many-loculed fruit, and tallvine is dominant over dwarf. A breeder has two purelines: (1) red, two-loculed, dwarf and (2) yellow, manyloculed, tall. From these two lines, he wants to produce anew pure line for trade that is yellow, two-loculed, andtall. How exactly should he go about doing so? Show notonly which crosses to make, but also how many progenyshould be sampled in each case.

Name: In tomatoes, red fruit is dominant over yellow, two-loculed fruit is d
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Description: In tomatoes, red fruit is dominant over yellow, two-loculed fruit is dominant over many-loculed fruit, and tallvine is dominant over dwarf. A breeder has two purelines: (1) red, two-loculed, dwarf and (2) yellow, manyloculed, tall. From these two lin

Concepts of Biology

1st Edition

ISBN:9781938168116

Author:Samantha Fowler, Rebecca Roush, James Wise

Publisher:Samantha Fowler, Rebecca Roush, James Wise

Chapter8: Patterns Of Inheritance

Section: Chapter Questions

Problem 2ACQ: Figure 8.10 In pea plants, purple flowers (P) are dominant to white (p), and yellow peas (Y) are...

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. A corn geneticist has three pure lines of genotypes a/a ; B/B ; C/C, A/A ; b/b ; C/C, and A/A ; B/B ; c/c. All the phenotypes determined by a, b, and c will increase the market value of the corn; so, naturally, he wants to combine them all in one pure line of genotype a/a ; b/b ; c/c. a. Outline an effective crossing program that can be used to obtain the a/a ; b/b ; c/c pure line. b. At each stage, state exactly which phenotypes will be selected and give their expected frequencies. c. Is there more than one way to obtain the desired genotype? Which is the best way?Assume independent assortment of the three gene pairs. (Note: Corn will self or cross-pollinate easily.
A cross was made between two pea plants, TtAa and Ttaa, whereT = tall, t = dwarf, A = axial, and a = terminal. What is the probability that the first three offspring will be tall with axial flowers or dwarf with terminal flowers and the fourth offspring will be tall with axial flowers? Discuss what operation(s) (e.g., product rule or binomial expansion equation) you used and in what order they were used
For a specific example, you might assume that four members of this pedigree are albinos: the woman in the first generation, her second daughter (the mother of individuals 5, 6, 7, and 8), and individuals 4 and 11 in the third generation. Now, assume that you are a genetic counselor and that individuals 6 and 12 in the third generation of this pedigree come to you and ask, “What is the probability that if we marry and have a family, an albino child will be born to us?” The counselor must determine the probability that individuals 6 and 12 are heterozygous carriers of the recessive gene for albinism. The counselor must also consider the probability of two heterozygous carriers producing a homozygous recessive child. First of all, the mother of individual 6 is an albino (cc), which means that 6 must be (probability = 1 or 100%) a heterozygote. The father of individual 12 must be heterozygous (Cc) since his mother is an albino. Although individual 12 is not an albino, he has a ½ chance of…
A plant breeder wants to use selective breeding to produce corn with short stalks and a high mass of grain.He could use the following varieties of cor, A, Long stalks, high mass of grain, B, Short stalks, low mass of grain or c, Long Stalks, low mass of grain. What would the plant breeder need to do to make sure he always produced corn with a short stem and a high mass of grain? Describe three steps the breeder would use.
Figure 8.10 In pea plants, purple flowers (P) are dominant to white (p), and yellow peas (Y) are dominant to green (y). What are the possible genotypes and phenotypes for a cross between PpYY and ppYy pea plants? How many squares would you need to complete a Punnett square analysis of this cross?
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 decide to have a child if the test results said that you carry the mutation for breast and ovarian cancer? The heart disease mutation? The TSD mutation? The heart disease and the mutant alleles?
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?
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. 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?
Two true-breeding varieties of maize, one 11 cm high and the other 47 cm high were crossed and the resultant F1 hybrids were then crossed to generate the F2 . In the F2 there were a total of 13,923 plants with a continuous variation in heights between the two extremes and with only 3 plants as large as 47 cm high and 5 plants of 11 cm high.So What would be the size and genotype of the F1 from a cross between a true-breeding 11 cm plant and a true-breeding 47 cm plant?
You self-fertilize an F1 plant to produce the F2 generation. Based on Mendelian principles of inheritance, what fraction of the F2 generation do you expect to be short with round, green seeds? HINT: Solving this problem will require a very large Punnett square (8 x 8), but you can easily solve it using the Multiplication Rule
A plant geneticist is examining the mode of inheritance of flower color in two closely related species of exotic plants. The first species may have two pure-breeding lines—one produces a distinct red flower; and the other produces flowers with no color at all, or very pale yellow flowers. However, she cannot be sure. A cross of these varieties produces all pink-flowered progeny. The second species exhibits similar pure-breeding varieties; that is, one variety produces red flowers; and the other produces an albino or very pale yellow flower. A cross of these two varieties, however, produces orange-flowered progeny exclusively. Analyze the mode of inheritance of flower color in these two plant species.
Two true-breeding varieties of maize, one 11 cm high and the other 47 cm high were crossed and the resultant F1 hybrids were then crossed to generate the F2 . In the F2 there were a total of 13,923 plants with a continuous variation in heights between the two extremes and with only 3 plants as large as 47 cm high and 5 plants of 11 cm high. What would be the size and genotype of the F1 from a cross between a true-breeding 11 cm plant and a true-breeding 47 cm plant? Please answer the following problem & EXPLAIN your answer showing ALL WORKING.