Concepts of Genetics Plus Mastering Genetics with Pearson eText -- Access Card Package (12th Edition) (What's New in Genetics)
12th Edition
ISBN: 9780134811390
Author: William S. Klug, Michael R. Cummings, Charlotte A. Spencer, Michael A. Palladino, Darrell Killian
Publisher: PEARSON
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Chapter 8, Problem 13PDQ
Discuss Ohno’s hypothesis on the role of gene duplication in the process of evolution. What evidence supports this hypothesis?
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Discuss the role of mutation in the origin of genetic polymorphisms. Suppose that a genetic polymorphism involves two alleles at frequencies of 0.45 and 0.55. Describe three different scenarios to explain these observed allele frequencies. You can propose that the mutations that produced the polymorphism are neutral, beneficial, or deleterious.
Who was Gregor Mendel? Why is he important in the history of science, and more specifically, in the history of Darwin's theory of evolution?
How can you use this piece of information to help you explain to your friends what is the significance of mutations in the emergence of new genetic properties (alleles) that may result (or not) in new phenotypic characteristics? (Recall that not all SNPs affect phenotype.)
Chapter 8 Solutions
Concepts of Genetics Plus Mastering Genetics with Pearson eText -- Access Card Package (12th Edition) (What's New in Genetics)
Ch. 8 - A human female with Turner syndrome (47, X) also...Ch. 8 - When two plants belonging to the same genus but...Ch. 8 - What is the effect of a rare double crossover (a)...Ch. 8 - Controlling the overgrowth of invasive aquatic...Ch. 8 - Controlling the overgrowth of invasive aquatic...Ch. 8 - Controlling the overgrowth of invasive aquatic...Ch. 8 - HOW DO WE KNOW? In this chapter, we have focused...Ch. 8 - Review the Chapter Concepts list on page 171....Ch. 8 - Define these pairs of terms, and distinguish...Ch. 8 - For a species with a diploid number of 18,...
Ch. 8 - What evidence suggests that Down syndrome is more...Ch. 8 - What evidence indicates that humans with aneuploid...Ch. 8 - Contrast the fertility of an allotetraploid with...Ch. 8 - Describe the origin of cultivated American cotton.Ch. 8 - Predict how the synaptic configurations of...Ch. 8 - Inversions are said to suppress crossing over. Is...Ch. 8 - Contrast the genetic composition of gametes...Ch. 8 - Human adult hemoglobin is a tetramer containing...Ch. 8 - Discuss Ohnos hypothesis on the role of gene...Ch. 8 - What roles have inversions and translocations...Ch. 8 - The primrose, Primula kewensis, has 36 chromosomes...Ch. 8 - Certain varieties of chrysanthemums contain 18,...Ch. 8 - Drosophila may be monosomic for chromosome 4, yet...Ch. 8 - Mendelian ratios are modified in crosses involving...Ch. 8 - Having correctly established the F2 ratio in...Ch. 8 - The mutations called bobbed in Drosophila result...Ch. 8 - The outcome of a single crossover between...Ch. 8 - A couple planning their family are aware that...Ch. 8 - In a cross in Drosophila, a female heterozygous...Ch. 8 - A woman who sought genetic counseling is found to...Ch. 8 - Prob. 25ESPCh. 8 - In a recent cytogenetic study on 1021 cases of...Ch. 8 - A boy with Klinefelter syndrome (47,XXY) is born...Ch. 8 - Prob. 28ESPCh. 8 - A 3-year-old child exhibited some early indication...Ch. 8 - A normal female is discovered with 45 chromosomes,...
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Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
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- 1. What is an allele? 2. What is a point mutation? 3. How are point mutations related to alleles? Use these sites to find the answer please: https://www.britannica.com/story/whats-the-difference-between-a-gene-and-an-allele http://rosalind.info/glossary/point-mutation/arrow_forwardWrite a paragraph describing the evolutionary forces driving changes in the human genome. You can include evolutionary forces such as random genetic drift, mutation, migration, and natural selection. These forces would have long-term and short-term effects on coding and non-coding DNA, the abundance of transposable elements, and the birth and death of genes. You can focus on a subset of the human population, or the entire species.arrow_forwardGeneticists study mitochondrial and Y-chromosome DNA to determine the ancestry of modern humans. Such studies have led to the emergence of mitochondrial Eve and Y-chromosome Adam, whose features above are a far-cry from an artist's interpretation of the Biblical narrative. Their progeny came to have the range of physical features now described as racial differences. How has modern genomics contributed to the debate about the validity and definition of these hypothetical parents and their descendants? References:arrow_forward
- The tiny frog Paedophryne amauensis was discovered by researchers purposefully searching for the source of an unusual sound, but sometimes similarity between two species can lead scientists to accidental discoveries. A previously unknown species of wild cat was inadvertently discovered by researchers who were sequencing the DNA of a house cat–sized South American wild cat called the tigrina. The DNA analysis revealed that many alleles found in the supposed tigrinas living in northeastern Brazil are not shared with other tigrinas. This finding suggested that the northeastern cats do not interbreed with other tigrinas and are therefore a different species. What prevents the two species from interbreeding?arrow_forwardChoose one human multifactorial condition and describe it in detail. Include a description of the condition, possible genetic and environmental components that cause the condition as well as an explanation of why it is difficult to study multifactorial conditions. Include references. PDF https://www.genetics.edu.au/PDF/Environmental_and_genetic_interactions_fact_sheet-CGE.pdfarrow_forwardGeneticists study mitochondrial and Y-chromosome DNA to determine the ancestry of modern humans. Such studies have led to the emergence of mitochondrial Eve and Y-chromosome Adam, whose features above are a far-cry from an artist's interpretation of the Biblical narrative. Their progeny came to have the range of physical features now described as racial differences. How has modern genomics contributed to the debate about the validity and definition of these hypothetical parents and their descendants?arrow_forward
- A neutral mutation arises in a diploid population of 10,000 individuals. Use this information to answer the following questions. a) What is the probability that the neutral allele goes to fixation? b) Assuming that the neutral mutation eventually goes to fixation, what is the expected time to fixation (in generations)?arrow_forwardIn a study of a muscle disorder, several affected families exhibited vision problems, muscle weakness, and deafness (M. Zeviani et al. 1990. American Journal of Human Genetics 47:904–914). Analysis of the mtDNA from affected members of these families revealed that large numbers of their mtDNA molecules possessed deletions of varying lengths. Different members of the same family and even different mitochondria from the same person possessed deletions of different sizes, so the underlying defect appeared to be a tendency for the mtDNA of affected persons to have deletions. A pedigree of one of the families studied is shown below. The researchers concluded that this disorder is inherited as an autosomal dominant trait, and they mapped the diseasecausing gene to a position on chromosome 10 in the nucleus. Q. What characteristics of the pedigree rule out inheritance of a trait encoded by a gene in the mtDNA as the cause of this disorder?arrow_forwardIn a study of a muscle disorder, several affected families exhibited vision problems, muscle weakness, and deafness (M. Zeviani et al. 1990. American Journal of Human Genetics 47:904–914). Analysis of the mtDNA from affected members of these families revealed that large numbers of their mtDNA molecules possessed deletions of varying lengths. Different members of the same family and even different mitochondria from the same person possessed deletions of different sizes, so the underlying defect appeared to be a tendency for the mtDNA of affected persons to have deletions. A pedigree of one of the families studied is shown below. The researchers concluded that this disorder is inherited as an autosomal dominant trait, and they mapped the diseasecausing gene to a position on chromosome 10 in the nucleus. Q. Explain how a mutation in a nuclear gene might lead to deletions in mtDNA.arrow_forward
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