Biology
5th Edition
ISBN: 9781260487947
Author: BROOKER
Publisher: MCG
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 15, Problem 4TY
Summary Introduction
Introduction: Those factors which cause the mutations are known as mutagens. The mutagens can be derived from the environment such as UV lights or x-rays. The influence of high amount of mutagen on an organism can lead to the formation of thymine dimer, which is very harmful to the organism.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Mutagens can cause mutations bya. chemically altering DNA nucleotides.b. disrupting DNA replication.c. altering the genetic code of an organism.d. all of the above.e. a and b only.
Which of the following is NOT true about mutations?
A. Mutations can be harmful but not beneficial to the cell
B. Nucleotide substitution in DNA can cause nonsense mutations
C. Nucleotide substitution in DNA can cause missense mutations
D. Mutagens increase the rate of mutation, but mutations are still random
E. Nucleotide insertion or deletion in DNA can cause frameshift mutations
Which of the following terms refer to the case when a mutation results in a significant decrease or a complete loss of the functional activity of a gene product?
a. gain-of-function mutation
b. loss-of-function mutation
Chapter 15 Solutions
Biology
Ch. 15.1 - Consequences of Mutations Concept Check: Based on...Ch. 15.1 - Prob. 2CCCh. 15.2 - Prob. 1EQCh. 15.2 - Prob. 2EQCh. 15.2 - Prob. 3EQCh. 15.2 - Prob. 1CCCh. 15.3 - DNA Repair Concept Check: Which components of the...Ch. 15.3 - Why is this person so sensitive to sunlight?...Ch. 15.4 - Prob. 1CCCh. 15.4 - Prob. 2CS
Ch. 15.4 - Prob. 2CCCh. 15.4 - Prob. 3CCCh. 15.4 - Prob. 4CCCh. 15 - Prob. 1TYCh. 15 - Prob. 2TYCh. 15 - Prob. 3TYCh. 15 - Prob. 4TYCh. 15 - Prob. 5TYCh. 15 - The Ames test a. provides a way to determine if...Ch. 15 - Xeroderma pigmentosum a. is a genetic disorder...Ch. 15 - Prob. 8TYCh. 15 - Prob. 9TYCh. 15 - Prob. 10TYCh. 15 - Prob. 1CQCh. 15 - Prob. 2CQCh. 15 - Prob. 3CQCh. 15 - Prob. 1COQCh. 15 - Distinguish between spontaneous and induced...
Knowledge Booster
Learn more about
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
- When using gene therapy to treat an hereditary disease, the idea is to: A. Introduce the correct gene into the patient's DNA B. Inject the patient with a specific protein to cure the disease. C. Blood transfusions from healthy individuals. D. ntroduce mRNA molecules with the correct genetic information to the patient. E. Introduce a virus to the patient that will specifically destroy mutated cells.arrow_forwardA SNV mutation that results in no change in the amino acid sequence is called: A. silent mutation B. silencing mutation C. missense mutation D. nonsense mutation E. frameshift mutationarrow_forwardWhich of the following is true about the enzyme telomerase? A. It is found only in adult cells. B. It is responsible for telomere shortening. C. It can re-establish telomere length. D. It may speed up the aging process. E. It is expressed at low levels in cancer cells.arrow_forward
- Induced mutations A. are a random change in the DNA arising from errors in replications B. are a result of exposure to a mutagen C. always have a positive effect on the organism D. always have a negative effect on the organismarrow_forwardWhich of the following types of mutations will have the most devastating effect on a cell?A.frameshift mutationB. missense mutationC. nonsense mutationD. silent mutationarrow_forwardWhich of the following is an example of a somatic mutation? a. A mutation in an embryonic muscle cell b. A mutation in a sperm cell c. A mutation in an adult nerve cell The somatic cells are all cells of the body excluding the d. Both a and c are examples of somatic mutations.arrow_forward
- A genetic researcher notices that individuals with a particular genetic disease have a shortened version of key protein involved in the diseased biochemical pathway. Which of the following mutations is most likely to result in the premature termination of protein synthesis? A. The disease is caused by a silent mutation. B. The disease is caused by a frameshift mutation. C. The disease is caused by a missense mutation. D. The disease is caused by a nonsense mutation.arrow_forwardWhich statement(s) below regarding DNA mutations is true: A. Mutations only occur in genes B. Mutations always result in phenotypic alterations C. Mutations are only induced by extrinsic (environmental) factors D. Mutations can occur in promoters E. Point mutations can be caused by transposons or “jumping genes”arrow_forwardA mutation changes a codon that specifies tyrosine into a stopcodon. This type of mutation is aa. missense mutation.b. nonsense mutation.c. frameshift mutation.d. neutral mutation.arrow_forward
- Which of the following is true about DNA manipulation? Select the best answer. A. all of these B. DNA has never been transferred between different organisms. C. Transferring DNA from one organism into another always kills the host organism. D. Whole genomes have been manipulated by humans for centuries; now individual genes ca be inserted into different organisms using a variety of techniques. E. DNA can't be manipulated.arrow_forwardMethylation can alter the process of gene expression because: B. By causing DNA to coil more tightly. A. By derailing the cellular transcription machinery. C. By removing the gene from the genome altogether. D. ALL answers A, B and C are correct. E. Only answers A and B are correct, but not C.arrow_forwardA.) There is no change in the DNA sequence if nucleotides are added or removed, it will have no effect to the cell. B.) Mutations in the DNA sequence are all irreversible. A. Statement A is correct B. Statement B is correct C. Both A and B are correct D. Both A and B are incorrectarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Human Anatomy & Physiology (11th Edition)BiologyISBN:9780134580999Author:Elaine N. Marieb, Katja N. HoehnPublisher:PEARSON
Biology 2eBiologyISBN:9781947172517Author:Matthew Douglas, Jung Choi, Mary Ann ClarkPublisher:OpenStax
Anatomy & 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 & Company
Laboratory 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
Human Anatomy & Physiology (11th Edition)
Biology
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:PEARSON
Biology 2e
Biology
ISBN:9781947172517
Author:Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher:OpenStax
Anatomy & Physiology
Biology
ISBN:9781259398629
Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa Stouter
Publisher:Mcgraw Hill Education,
Molecular Biology of the Cell (Sixth Edition)
Biology
ISBN:9780815344322
Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter Walter
Publisher:W. W. Norton & Company
Laboratory Manual For Human Anatomy & Physiology
Biology
ISBN:9781260159363
Author:Martin, Terry R., Prentice-craver, Cynthia
Publisher:McGraw-Hill Publishing Co.
Inquiry Into Life (16th Edition)
Biology
ISBN:9781260231700
Author:Sylvia S. Mader, Michael Windelspecht
Publisher:McGraw Hill Education
Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY