Essentials of Genetics, Books a la Carte Plus Mastering Genetics with eText -- Access Card Package (9th Edition)
9th Edition
ISBN: 9780134319070
Author: William S. Klug, Michael R. Cummings, Charlotte A. Spencer, Michael A. Palladino
Publisher: PEARSON
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Chapter 14, Problem 2PDQ
Review the Chapter Concepts list on page 257. These concepts relate to how gene mutations occur, their
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In McCune-Albright syndrome, fibrous connective tissue replaces bone, tan patches (café-au-lait spots) dot the skin, and hormone abnormalities cause early puberty and malfunction of the thyroid, pituitary, and adrenal glands. The phenotype is highly variable, and all patients are somatic mosaics for the mutation, which is in the gene GNAS1. Why is the condition seen only in mosaics?
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Chapter 14 Solutions
Essentials of Genetics, Books a la Carte Plus Mastering Genetics with eText -- Access Card Package (9th Edition)
Ch. 14 - CASE STUDY| Genetic dwarfism Seven months...Ch. 14 -
CASE STUDY | Genetic dwarfism
Seven months...Ch. 14 -
CASE STUDY| Genetic dwarfism
Seven months...Ch. 14 - CASE STUDY | Genetic dwarfism Seven months...Ch. 14 -
HOW DO WE KNOW?
1. In this chapter, we focused on...Ch. 14 - Review the Chapter Concepts list on page 257....Ch. 14 - What is a spontaneous mutation, and why are...Ch. 14 -
4. Why would a mutation in a somatic cell of a...Ch. 14 - Why is a random mutation more likely to be...Ch. 14 - Most mutations in a diploid organism are...
Ch. 14 - What is meant by a conditional mutation?Ch. 14 -
8. Describe a tautomeric shift and how it may...Ch. 14 - Contrast and compare the mutagenic effects of...Ch. 14 - Why are frameshift mutations likely to be more...Ch. 14 - Why are X rays more potent mutagens than UV...Ch. 14 -
12. DNA damage brought on by a variety of natural...Ch. 14 - Contrast the various types of DNA repair...Ch. 14 -
14. Mammography is an accurate screening...Ch. 14 - Describe how the Ames test screens for potential...Ch. 14 - What genetic defects result in the disorder...Ch. 14 - In a bacterial culture in which all cells are...Ch. 14 - Human equivalents of bacterial DNA mismatch repair...Ch. 14 - A number of different types of mutations in the...Ch. 14 -
20. Some mutations that lead to diseases such as...Ch. 14 - In maize, a Ds or Ac transposon can cause...Ch. 14 -
22. Presented here are hypothetical findings from...Ch. 14 -
23. Cystic fibrosis (CF) is a severe autosomal...Ch. 14 -
24. Electrophilic oxidants are known to create...Ch. 14 - Skin cancer carries a lifetime risk nearly equal...Ch. 14 -
26. The initial discovery of IS elements in...Ch. 14 -
27. It is estimated that about 0.2 percent of...Ch. 14 -
28. It has been noted that most transposons in...Ch. 14 - Two related forms of muscular dystrophy–Duchenne...
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- Which of the following is true regarding the presence of a multigene family? A. Multigene families are produced by any sort of chromosomal rearrangement. B. Multigene families are produced whenever a transposon is inserted into a gene. C. Multigene families are produced by all types of mutation, including single base substitutions. D. Multigene families are produced by some mutations that involve duplication.arrow_forwardplease solve the following: (a)Explain how a mutation effects a genotype. (b) Explain how a mutation may or may not effect a phenotype. (c)What is the difference between DNA replication, transcription, and translation. What are the products in each, and what are they used for? please solve accurate and exact.arrow_forwardIn the lab, you discover two yeast haploid mutants that cannot produce arginine. You cross them together and the resulting diploid produces arginine. If producing arginine is the wild type phenotype, what can you definitively conclude? A.The haploid strains have identical mutations in the same genes. B.The haploid strains have identical mutations in different genes. C.The haploid strains have mutations in different genes. D.The haploid strains have mutations in the same gene. E.The haploid strains must belong to the complementation group encoding the first enzyme in the biosynthetic pathway.arrow_forward
- Theodor Boveri predicted that malignancies would often be associated with chromosomal mutation. What lines of evidence substantiate this prediction?arrow_forwardWhat is a homolog? With regard to genes and alleles, how arehomologs similar to and different from each other?arrow_forwardOne of the following is most suitable for study of mutations: A. Haploids B. Diploids C. Tetraploids D. Polyploidarrow_forward
- Describe how you would use replica plating of mutagenized, haploid yeast cells to identify temperature-sensitive (ts) mutations in essential genes needed for yeast growth and survival.arrow_forwardDiscuss how ultra violet light works as a mutagen. This could include: What is UV light and the Mutations commonly introduced by UV light? What are the Repair mechanisms in yeast that fix damage caused by UV light? Describe the phenotypes of Saccharomyces Cerevisiae plates, the first plate is the control yeast, while the second plate has been exposed to low UV light, the third plate has been exposed to high UV light. Normal yeast has round smooth white colonies. Are there any signinifcant differences?arrow_forwardExplain why, in humans, chromosomal mutation rates in females are much higher than in males.arrow_forward
- In a particular strain of Neurospora, a poky mutation exhibits biparental inheritance, whereas poky mutations in other strains are inherited only from the maternal parent. Explain these results.arrow_forwardWhat impact does the environment have on traits? Explain how pleiotropy impacts traits. Discuss basic steps in prokaryotic gene regulationarrow_forwardThe origin of genes that have new functions often involves the divergence of gene duplicates.Duplicates can arise via several mechanisms. a. One mechanism of gene duplication is retrotransposition, the insertion into the genome of DNA produced by reverse transcription of a messenger RNA. These gene duplicates are often dead on arrival: they are pseudogenes as soon as they are formed. Why are such duplicates so often dead on arrival? b. A second mechanism of gene duplication occurs via unequal crossing over during meiosis. Gene duplicates formed this way are functional more often than when they arise by reverse transcription. Why is that? c. If a gene duplicate is initially functional, what are its possible ultimate fates? Which is most likely,and why?arrow_forward
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