Concept explainers
To explain:
The process of occurrence of mutations and the consequences of point mutation and frameshift mutation.
Introduction:
A permanent change in the cell’s DNA is called mutation. This change occurs in the

Answer to Problem 40A
Mutations are caused by errors in replication, transcription, cell division or by some external agents.
Point mutation- It occurs when one base pair is altered. They are of two types; missense and nonsense. Missense code for wrong amino acid and nonsense change the codon for amino acid to stop codon. Nearly all nonsense mutations lead to proteins that cannot function normally.
Frameshift mutation- Insertion and deletions of a nucleotide causes a shift in frame of the amino acid sequence.
These mutations often lead to many diseases and disorders. Some mutations may be advantageous to an organism as it may help it to survive in harsh conditions better. Mutations provide new variations and these variations are involved in natural selection.
Explanation of Solution
Point mutation- A point mutation is one that involves a chemical change in just one base pair. Substitution is a type of point mutation. This occurs when one base is exchanged for another base. Most substitutions are missense mutations, where the genetic code is altered so that it codes for the wrong amino acid. Other substitutions called nonsense mutations change the codon for an amino acid to a stop codon. These cause translation to stop immediately.
Frameshift mutation- Insertions occur when a nucleotide is added to the DNA sequence. Deletion occurs when a nucleotide is removed from a DNA sequence.These types of mutations change the multiples of three codons from the point of insertion/ deletion. Hence they are called frame-shift mutation because they change the “frame” of the amino acid.
The cumulative effect of mutations in a population might cause a change in allelic frequencies, and thus violate genetic equilibrium. Many mutations are lethal or harmful but some may be good for the organism. This mutation will be selected for and become more common in subsequent generations. In this way, mutations provide a raw material upon which natural selection works.
Chapter 15 Solutions
EP BIOLOGY 2012-STUDENTWORKS ONLINE
Additional Science Textbook Solutions
Cosmic Perspective Fundamentals
Concepts of Genetics (12th Edition)
Chemistry: A Molecular Approach (4th Edition)
The Cosmic Perspective (8th Edition)
Human Anatomy & Physiology (2nd Edition)
College Physics: A Strategic Approach (3rd Edition)
- If using animals in medical experiments could save human lives, is it ethical to do so? In your answer, apply at least one ethical theory in support of your position.arrow_forwardYou aim to test the hypothesis that the Tbx4 and Tbx5 genes inhibit each other's expression during limb development. With access to chicken embryos and viruses capable of overexpressing Tbx4 and Tbx5, describe an experiment to investigate whether these genes suppress each other's expression in the limb buds. What results would you expect if they do repress each other? What results would you expect if they do not repress each other?arrow_forwardYou decide to delete Fgf4 and Fgf8 specifically in the limb bud. Explain why you would not knock out these genes in the entire embryo instead.arrow_forward
- You implant an FGF10-coated bead into the anterior flank of a chicken embryo, directly below the level of the wing bud. What is the phenotype of the resulting ectopic limb? Briefly describe the expected expression domains of 1) Shh, 2) Tbx4, and 3) Tbx5 in the resulting ectopic limb bud.arrow_forwardDesign a grafting experiment to determine if limb mesoderm determines forelimb / hindlimb identity. Include the experiment, a control, and an interpretation in your answer.arrow_forwardThe Snapdragon is a popular garden flower that comes in a variety of colours, including red, yellow, and orange. The genotypes and associated phenotypes for some of these flowers are as follows: aabb: yellow AABB, AABb, AaBb, and AaBB: red AAbb and Aabb: orange aaBB: yellow aaBb: ? Based on this information, what would the phenotype of a Snapdragon with the genotype aaBb be and why? Question 21 options: orange because A is epistatic to B yellow because A is epistatic to B red because B is epistatic to A orange because B is epistatic to A red because A is epistatic to B yellow because B is epistatic to Aarrow_forward
- A sample of blood was taken from the above individual and prepared for haemoglobin analysis. However, when water was added the cells did not lyse and looked normal in size and shape. The technician suspected that they had may have made an error in the protocol – what is the most likely explanation? The cell membranes are more resistant than normal. An isotonic solution had been added instead of water. A solution of 0.1 M NaCl had been added instead of water. Not enough water had been added to the red blood cell pellet. The man had sickle-cell anaemia.arrow_forwardA sample of blood was taken from the above individual and prepared for haemoglobin analysis. However, when water was added the cells did not lyse and looked normal in size and shape. The technician suspected that they had may have made an error in the protocol – what is the most likely explanation? The cell membranes are more resistant than normal. An isotonic solution had been added instead of water. A solution of 0.1 M NaCl had been added instead of water. Not enough water had been added to the red blood cell pellet. The man had sickle-cell anaemia.arrow_forwardWith reference to their absorption spectra of the oxy haemoglobin intact line) and deoxyhemoglobin (broken line) shown in Figure 2 below, how would you best explain the reason why there are differences in the major peaks of the spectra? Figure 2. SPECTRA OF OXYGENATED AND DEOXYGENATED HAEMOGLOBIN OBTAINED WITH THE RECORDING SPECTROPHOTOMETER 1.4 Abs < 0.8 06 0.4 400 420 440 460 480 500 520 540 560 580 600 nm 1. The difference in the spectra is due to a pH change in the deoxy-haemoglobin due to uptake of CO2- 2. There is more oxygen-carrying plasma in the oxy-haemoglobin sample. 3. The change in Mr due to oxygen binding causes the oxy haemoglobin to have a higher absorbance peak. 4. Oxy-haemoglobin is contaminated by carbaminohemoglobin, and therefore has a higher absorbance peak 5. Oxy-haemoglobin absorbs more light of blue wavelengths and less of red wavelengths than deoxy-haemoglobinarrow_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





