Concept explainers
Identify two general ways chemical mutagens can alter DNA. Give examples of these two mechanisms.
To review:
Analyze how chemical mutagens can alter DNA. Give examples of these two mechanisms of chemical mutation.
Introduction:
Mutation can be defined as a heritable change in the DNA sequence. This change in the DNA sequences either leads to evolutionary change in the DNA, or it changes the gene sequence which disturbs its desirable function and affects the fitness of the organism. Mutation occurs very rarely and randomly. The physical or chemical substance which causes the mutation in the DNA is called the mutagen. Examples of the physical mutagens are radioactive substances, X-rays, and ultraviolet rays, and those of chemical mutagens are Nitrous acid, Acridine, proflavin and Base analogues.
Explanation of Solution
Chemical mutagen is the compound which causes mutation in DNA as it alters the sequence of the DNA. Types of chemical mutation:
1) Base analogue mutation
2) Intercalating agents
3) Deamination
4) Alkylating agents
1) Base analogue mutation: A base analogue is the chemical compound that mimics nitrogen bases and gets incorporated in place of normal base in the DNA. As these compounds are not the true base pair, they possess some different characters of the pairing to the complementary base pair. This wrong incorporation of the nitrogen base in the DNA leads to mutation.
A known example of the base analogue is
2) Intercalating agents: A chemical that loads itself in between the stacked bases of the DNA is called the intercalating agent. This intercalation of chemicals in DNA results in either insertion or deletion of the bases; this results in frameshift mutation of the DNA.
The examples of intercalating agents are Acridine orange, proflavin, and acriflavin. These dyes have a three ringed structure which resembles with purine- pyrimidine base pairing. Purine has a double ring structure while the pyrimidine has a single ring structure; when they pair, they form a three ring structure. When the dyes intercalate into the DNA, it results in the deletion or insertion of the of the DNA replication, therefore frameshift mutation.
A chemical mutagen causes changes in the sequence of the DNA, it is called chemical mutation.
Want to see more full solutions like this?
Chapter 12 Solutions
Genetic Analysis: An Integrated Approach (2nd Edition)
- Silent mutations that occur in DNA are quite common in living cells and usually involve no effects on phenotype. In not more than 2 pages (using 1.5 line space of Arial or Times New Roman fonts) provide answers for the following questions? 1) Define the silent mutation in DNA? 2) What is the codon usage bias? 3) Provide one example of a clinical implication of a “silent mutation” that proven to have an effect on the phenotype andprovide a brief description of its molecular characteristics? (Explain in details)arrow_forwardSilent mutations that occur in DNA are quite common in living cells and usually involve no effects on phenotype. In not more than 2 pages (using 1.5 line space of Arial or Times New Roman fonts) provide answers for the following questions? 1) Define the silent mutation in DNA? 2) What is the codon usage bias? 3) Provide one example of a clinical implication of a “silent mutation” that proven to have an effect on the phenotype andprovide a brief description of its molecular characteristics?arrow_forwardBriefly explain how site-directed mutagenesis is carried out.arrow_forward
- Distinguish between spontaneous and induced mutations. Give some examples of mutagens that cause induced mutations.arrow_forwarddescribe types of mutagens with 5 examples and their mutagenic effects and mechanismsarrow_forwardExplain how a mutagen can interfere with DNA replication to cause a mutation. Give two examples.arrow_forward
- please 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_forwardExposure to various chemicals can cause DNA mutations. Classify the examples as representative of transition, transversion, or nsertion/deletion mutations. Transition replacement of T:A: with C:G treatment with nitrogen mustard causes this type of mutation oxidative deamination via nitrous acid causes this type of mutation treatment with 5-bromouracil causes the replacement of A:T with G:C Transversion replacement of G:C with T:A Answer Bank Insertion/Deletion the removal of one or more base pairs treatment with proflavin causes this type of mutationarrow_forwardIt has been noted that most transposons in humans and other organisms are located in noncoding regions of the genome regions such as introns, pseudogenes, and stretches of particular types of repetitive DNA. There are several ways to interpret this observation. Describe two possible interpretations. Which interpretation do you favor? Why?arrow_forward
- Explain the rationale behind the use of the “bag of worms” phenotype as a way to identify heterochronic mutations.arrow_forwardDescribe in vitro mutagenesis and its potential uses.arrow_forwardhttps://www.khanacademy.org/science/biology/biotech-dna-technology/dna-cloning-tutorial/a/overview-dna-cloning That is the link for the example ^arrow_forward
- Human Anatomy & Physiology (11th Edition)BiologyISBN:9780134580999Author:Elaine N. Marieb, Katja N. HoehnPublisher:PEARSONBiology 2eBiologyISBN:9781947172517Author:Matthew Douglas, Jung Choi, Mary Ann ClarkPublisher:OpenStaxAnatomy & PhysiologyBiologyISBN:9781259398629Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa StouterPublisher:Mcgraw Hill Education,
- Molecular Biology of the Cell (Sixth Edition)BiologyISBN:9780815344322Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter WalterPublisher:W. W. Norton & CompanyLaboratory Manual For Human Anatomy & PhysiologyBiologyISBN:9781260159363Author:Martin, Terry R., Prentice-craver, CynthiaPublisher:McGraw-Hill Publishing Co.Inquiry Into Life (16th Edition)BiologyISBN:9781260231700Author:Sylvia S. Mader, Michael WindelspechtPublisher:McGraw Hill Education