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Ch. 14 - Gene Mutation, DNA Repair, and Transposition
Klug - Essentials of Genetics 10th Edition
Klug10th EditionEssentials of GeneticsISBN: 9780135588789Not the one you use?Change textbook
Chapter 14, Problem 16

Describe how the Ames test screens for potential environmental mutagens. Why is it thought that a compound that tests positively in the Ames test may also be carcinogenic?

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Explain that the Ames test is a biological assay used to assess the mutagenic potential of chemical compounds by observing their ability to cause mutations in the DNA of certain strains of bacteria, typically Salmonella typhimurium, which carry mutations making them unable to synthesize the amino acid histidine.
Describe how the test involves exposing these bacteria to the chemical compound in question and then plating them on a medium lacking histidine; only bacteria that undergo a reverse mutation restoring the ability to produce histidine will grow into colonies.
Clarify that an increased number of colonies compared to a control indicates that the compound induces mutations, suggesting it is a mutagen.
Discuss the connection between mutagenicity and carcinogenicity by explaining that mutations in DNA can lead to uncontrolled cell growth and cancer, so compounds that cause mutations in the Ames test are suspected to have carcinogenic potential.
Mention that while the Ames test is a useful initial screen, further testing in mammalian systems is necessary to confirm carcinogenicity because not all mutagens are carcinogens and vice versa.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Ames Test Methodology

The Ames test is a biological assay that uses specially engineered strains of bacteria to detect chemical substances that cause mutations. These bacteria are unable to grow on a medium lacking a specific nutrient unless a mutation reverses this defect. By exposing the bacteria to a test compound, the test identifies mutagens based on the number of colonies that regain growth ability, indicating induced mutations.
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Mutagens and Carcinogens Relationship

Mutagens are agents that cause changes in DNA sequences, which can disrupt normal cellular functions. Many carcinogens are mutagens because DNA mutations can lead to uncontrolled cell growth and cancer. Therefore, a positive Ames test suggests that a compound can cause genetic mutations, implying a potential to initiate carcinogenesis.
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Metabolic Activation in Ames Test

Some compounds are not directly mutagenic but become mutagenic after metabolic conversion in the body. The Ames test often includes a liver extract (S9 mix) to simulate this metabolic activation, allowing detection of pro-mutagens. This feature enhances the test’s relevance to real-world exposure and carcinogenic risk assessment.
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Related Practice
Textbook Question

Contrast the various types of DNA repair mechanisms known to counteract the effects of UV radiation. What is the role of visible light in repairing UV-induced mutations?

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Textbook Question

Mammography is an accurate screening technique for the early detection of breast cancer in humans. Because this technique uses X rays diagnostically, it has been highly controversial. Can you explain why? What reasons justify the use of X rays for such a medical screening technique?

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Textbook Question

A significant number of mutations in the HBB gene that cause human β-thalassemia occur within introns or in upstream noncoding sequences. Explain why mutations in these regions often lead to severe disease, although they may not directly alter the coding regions of the gene.

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Textbook Question

What genetic defects result in the disorder xeroderma pigmentosum (XP) in humans? How do these defects create the phenotypes associated with the disorder?

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Textbook Question

Compare DNA transposons and retrotransposons. What properties do they share?

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Textbook Question

In maize, a Ds or Ac transposon can alter the function of genes at or near the site of transposon insertion. It is possible for these elements to transpose away from their original insertion site, causing a reversion of the mutant phenotype. In some cases, however, even more severe phenotypes appear, due to events at or near the mutant allele. What might be happening to the transposon or the nearby gene to create more severe mutations?

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