You are tracing the inheritance of petal color in tropical sandflowers. You suspect that the inheritance follows a dominant epistasis inheritance pattern, based on the following data: 1204 white petals 296 orange petals 101 yellow petals Perform a statistical test to demonstrate whether the data matches your prediction of dominant epistasis. Record your work as much as you can. What is your overall conclusion about inheritance for this flower?

You are tracing the inheritance of petal color in tropical sandflowers. You suspect that the inheritance follows a dominant epistasis inheritance pattern, based on the following data: 1204 white petals 296 orange petals 101 yellow petals Perform a statistical test to demonstrate whether the data matches your prediction of dominant epistasis. Record your work as much as you can. What is your overall conclusion about inheritance for this flower?

Name: You are tracing the inheritance of petal color in tropical sandflowers
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Description: You are tracing the inheritance of petal color in tropical sandflowers. You suspect that the inheritance follows a dominant epistasis inheritance pattern, based on the following data: 1204 white petals296 orange petals101 yellow petals Perform a stat

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 5RQ: Imagine that you are performing a cross involving seed texture in garden pea plants. You cross...

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A heterozygous plant of AaBb genotype was testcrossed and gave the following results. Phenotypes A _B_ A_bb aaB_ aabb Number 140 38 32 150 Are genes A and B independently inherited? Show the mathematical basis of your decision. If genes A and B are not independently inherited, what could be the alternative mode of inheritance?
In a certain plant, the seed traits are as follows: Color: white (W) is dominant over yellow (w)Shape: disk (D) is dominant over sphere (d)Seed coat: thick (T) is dominant over thin (t) a) If the parent plant is a triple heterozygote, what is its phenotype? b) Analyzing the phenotypes of the offspring, the alleles of the gametes were determined as: 85 wDt 390 WDT 27 WDt 81 WdT5 wDT 374 wdt 30 wdT 8 Wdt construct a genetic map using the three-point cross.
A certain plant has 3 un-linked gene pairs, which can be represented as AaBbCc. Upon self-fertilization what proportion of the progeny will display the dominant phenotype with respect to genes A and B and the recessive phenotype for "c"? 3/64 1/64 16/64 32/64 9164
Shown in the pictures below are the degrees of dominance in the inheritance of flower color in some plants. *Based on the phenotypes (or maybe genotype), differentiate between complete dominance, incomplete dominance, and codominance. Be able to discuss the difference briefly but concisely. You may also refer to the definition.
Imagine that you are performing a cross involving seed texture in garden pea plants. You cross true-breeding round and wrinkled parents to obtain F1 offspring. Which of the following experimental results in terms of numbers of plants are closest to what you expect in the F2 progeny? a. 8lOroundseeds b. 8lOwrinkledseeds c. 405:395 round seeds:wrinkled seeds d. 610:190 round seeds:wrinkled seeds
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?
In a certain plant, the seed traits are as follows: Color: white (W) is dominant over yellow (w)Shape: disk (D) is dominant over sphere (d)Seed coat: thick (T) is dominant over thin (t) -If the parent plant is a triple heterozygote, what is its phenotype? Analyzing the phenotypes of the offspring, the alleles of the gametes were determined as: 85 wDt 390 WDT 27 WDt 81 WdT5 wDT 374 wdt 30 wdT 8 Wdt-Try to construct a genetic map using the three-point cross
In Mendel's genetic experiments many characteristics of the plants were quantified, such as their height (tall or short), flower position (axial or terminal), and seed color (colored or white). Suppose 100 plants are measured, and 37 are tall with axial flowers and colored seeds. Further, suppose a total of 26 plants have white seeds, 4 of them being short and 7 having terminal flowers. There are no short plants with terminal flowers, and the total number of short plants is 12. What is the probability a randomly selected plant will have flowers in the terminal position? Round your answer to THREE DECIMAL places. Also, double check your answer before posting. thank you
Consider the following hypothetical gene a plant.Gene T produces a protein that impacts stem length.There are two alleles for gene T, T which produces long stems and t which results in short stems. Assume that gene T displays complete dominance, what would be the genotypes (written as two letters-your answer will be case sensitive) that correspond to- homozygous dominant, homozygous recessive and heterozygous. and the phenotypes (what trait will be observed in the plant) for each of the genotypes.
Waxy endosperm (wx), shrunken endosperm (sh) and yellow seedling (v) are encoded by three recessive genes in corn that are linked on chromosome 5. A corn plant homozygous for all three recessive alleles is crossed with a plant homozygous for all the dominant alleles. The resulting F1 are then crossed with a plant homozygous for the recessive alleles in a three point test cross. The progeny of the test cross are: wx sh WX SH V WX SH V Wx sh WX sh V SH v SH V V 87 1,515 94 WX 1,531 3,479 292 WX Wx sh v 3,478 280 a. Determine the order of the genes on the chromosome. b. Calculate the map distances between the genes. c. Determine the cc and I.