Biology: The Dynamic Science (MindTap Course List)
4th Edition
ISBN: 9781305389892
Author: Peter J. Russell, Paul E. Hertz, Beverly McMillan
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Videos
Question
Chapter 13, Problem 2ITD
Summary Introduction
To review:
The relationship between smoking and the formation of adducts.
Introduction:
Oral or mouth cancers are caused due to smoking and chewing of tobacco. This can lead to mutations in offspring. The exchange of genetic material between two homologous chromosomes is called crossover of chromosome. This process is responsible for recombinant DNA (deoxyribonucleic acid). The depiction of the recombination frequencies between the genetic markers during crossovers is called the genetic map. The space between two genetic markers is given by the crossover frequencies.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
The dominant condition elliptocytosis causes red blood cells to become misshapen into oval-shaped cells. One of the genes responsible for the abnormal shape encodes the band 4.1 protein that together with ankyrin and other scaffold proteins creates and maintains the spherical concave shape of a normal red blood cell. The gene for band 4.1 protein, EPB41, is found on the p arm of chromosome 1. This is very close to the gene encoding the red blood cell Rhesus (Rh) blood type, either phenotype + (dominant) or - (recessive), with a recombination frequency of 2%. This means that 98% of the time alleles for these two genes are linked and are transmitted together.
Diane and Jack are siblings, and both have elliptocytosis and Rh+ blood type. Due to the elliptocytosis, both had emergency splenectomies after having severe anemia. Their younger brother, Devonté, has not yet shown signs of elliptocytosis, but has Rh- blood. André, their dad, also has elliptocytosis and Rh+ blood; while their…
the deletion of which chromosome causes obvious morphological and mental defects in the organism, such as microcephaly, strabismus, major mental retardation and is known as the 'cri-du-chat' syndrome?
Are mutations that arise during mitosis or meiosis the same? Explain in 15 sentences.
Chapter 13 Solutions
Biology: The Dynamic Science (MindTap Course List)
Ch. 13.1 - You want to determine whether genes a and b are...Ch. 13.2 - You have a true-breeding strain of...Ch. 13.3 - What mechanisms are responsible for: (a)...Ch. 13.4 - A man has Simpson syndrome, an addiction to a...Ch. 13.4 - Prob. 2SBCh. 13.5 - Prob. 1SBCh. 13 - In humans, redgreen color blindness is an X-linked...Ch. 13 - The following pedigree shows the pattern of...Ch. 13 - Individuals affected by a condition known as...Ch. 13 - A number of genes carried on the same chromosome...
Ch. 13 - Prob. 5TYKCh. 13 - Discuss Concepts Can a linkage map be made for a...Ch. 13 - In Drosophila, two genes, one for body color and...Ch. 13 - Another gene in Drosophila determines wing length....Ch. 13 - Prob. 9TYKCh. 13 - You conduct a cross in Drosophila that produces...Ch. 13 - Discuss Concepts Crossing-over does not occur...Ch. 13 - Prob. 12TYKCh. 13 - Prob. 13TYKCh. 13 - Prob. 14TYKCh. 13 - Prob. 1ITDCh. 13 - Prob. 2ITDCh. 13 - Prob. 3ITDCh. 13 - Prob. 4ITD
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
- Most forms of cancer are caused by environmental agents that produce mutations in somatic cells. Is an individual with cancer considered a genetic mosaic? Explain why or why not.arrow_forwardDiscuss why a genetic disease might have a particular age of onset.Would an infectious disease have an age of onset? Explain why orwhy not.arrow_forwardFragile X syndrome, caused by a change in the FMR1 gene, is the most common form of intellectual disability. In patients with this syndrome, a small part of the gene is repeated several times in one area of the chromosome. This defect in the gene makes the body unable to produce adequate amounts of a protein needed for normal brain functioning. In males, this syndrome causes a moderate intellectual disability, and in females, a mild intellectual disability. A family that exhibits Fragile X syndrome is shown in the pedigree. In the pedigree, squares represent males and circles represent females. Shaded symbols represent a person with the disorder. Which of the following correctly predicts the outcome if offspring 11 mated with a homozygous normal female, based on the inheritance pattern shown in the pedigree? A - The male offspring would exhibit Fragile X syndrome because Fragile X is an X-linked recessive trait. B - The female offspring would exhibit Fragile X syndrome because Fragile…arrow_forward
- Fragile X syndrome, caused by a change in the FMR1 gene, is the most common form of intellectual disability. In patients with this syndrome, a small part of the gene is repeated several times in one area of the chromosome. This defect in the gene makes the body unable to produce adequate amounts of a protein needed for normal brain functioning. In males, this syndrome causes a moderate intellectual disability, and in females, a mild intellectual disability. A family that exhibits Fragile X syndrome is shown in the pedigree. In the pedigree, squares represent males and circles represent females. Shaded symbols represent a person with the disorder. Which of the following correctly predicts the outcome if offspring 11 mated with a homozygous normal female, based on the inheritance pattern shown in the pedigree? The male offspring would exhibit Fragile X syndrome because Fragile X is an X-linked recessive trait. The female offspring would exhibit Fragile X syndrome because Fragile X…arrow_forwardA subset of colorectal cancers is associated with mutations in the Mut genes which code for proteins involved in repairing DNA mismatches. How would mutations in the Mut genes affect the DNA of an individual?arrow_forwardMost cells are unable to copy the ends of chromosomes, and therefore chromosomes shorten with each cell division. This limits the number of times a cell can divide. In germ cells and stem cells, however, an enzyme called telomerase lengthens the telomeres and prevents chromosome shortening. Thus, these cells are not limited in the number of times they can divide. All cells have the gene for telomerase, but most somatic cells don’t express it, and they produce no telomerase. Why don’t somatic cells express telomerase and have unlimited division?arrow_forward
- Chorionic villus sampling is a procedure to determine if there are any abnormalities in chromosome number in the fetus. Why can the chorionic villi be used to determine abnormalities in the fetus?arrow_forwardDescribe three examples of errors in cellular processes that lead to DNA duplications.arrow_forwardDefine the Genomic Instability in cancer cells ? What is leads to ?arrow_forward
- List and briefly define/describe 9 different DNA –related aging mechanisms.arrow_forward"In most differentiated tissues, daughter cells retain a memory of gene expression patterns that were present in the parent cell through mechanisms that do not involve changes in the sequence of their genomic DNA" is true or false.arrow_forwardWhich, if any, of the following statements is false? a) Most of the inherited changes in our DNA arise because of exposure to extracellular mutagens, including radiation sources and chemical mutagens. b) Most of the inherited changes in our DNA arise because of unavoidable endogenous errors in cellular mechanisms and harmful effects of certain natural molecules and atoms within our cells. c) Errors in DNA replication and DNA repair are a major source of mutations in our cells. d) Significant chemical damage is sustained by DNA because of its proximity to water molecules in our cells.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Biology: The Dynamic Science (MindTap Course List)BiologyISBN:9781305389892Author:Peter J. Russell, Paul E. Hertz, Beverly McMillanPublisher:Cengage Learning
Biology: The Dynamic Science (MindTap Course List)
Biology
ISBN:9781305389892
Author:Peter J. Russell, Paul E. Hertz, Beverly McMillan
Publisher:Cengage Learning
What are Mutations and what are the different types of Mutations?; Author: Science ABC;https://www.youtube.com/watch?v=I16YlE8qTBU;License: Standard youtube license