Biology: The Unity and Diversity of Life
Biology: The Unity and Diversity of Life
15th Edition
ISBN: 9780357093795
Author: STARR
Publisher: CENGAGE LEARNING (CUSTOM)
bartleby

Concept explainers

Question
Book Icon
Chapter 13, Problem 1DAA
Summary Introduction

To explain: The number of Ty2 strain of Salmonella typhi that was able to enter normal cells than cells heterozygous for the ΔF508 allele.

Introduction: An allele is the modification of the gene. Salmonella typhi is the causative bacteria of typhoid. Cystic fibrosis (CF) is a genetic disorder caused due to the inability of the cell to perform endocytosis due to a mutation in the CFTR gene. Cystic fibrosis affects the lungs, intestine, liver, and kidneys. Endocytosis is a phenomenon where the cell takes up molecules by engulfing with its membrane. The S. typhi exploits this mechanism to infect the intestinal cell and causes diarrhea. The cells that are homozygous for this CFTR mutation cannot perform endocytosis, and the S. typhi cannot infect those individuals.

Expert Solution & Answer
Check Mark

Explanation of Solution

Scientist G along with his colleagues studied the uptake of S. typhi by two types of epithelial cells:

  • Cells that are homozygous for the normal alleles.
  • Cells that are heterozygous for ΔF508 allele associated with CF and the normal alleles.

Cells that are homozygous for the mutant allele do not take up S. typhi; therefore, those cells were not chosen. A bar graph was drawn with three strains of S. typhi on the X-axis, and the number of bacteria internalized by both types of cells in the Y-axis.

Approximately, 600,000 S. typhi entered the normal cells that are homozygous for the normal alleles.

Approximately, 80,000 S. typhi entered the mutated cells that are heterozygous for ΔF508 allele associated with CF and normal alleles.

Therefore, the number of times more S. typhi entered normal cells than heterozygous cells can be calculated as follows:

Number oftimes moreS. typhi entered normal cells=60000080000=7.5

Conclusion

Therefore, about 7.5 times more S. typhi entered the normal cells.

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
. Mutations in an autosomal gene in humans cause aform of hemophilia called von Willebrand disease(vWD). This gene specifies a blood plasma proteincleverly called von Willebrand factor (vWF). vWFstabilizes factor VIII, a blood plasma protein specified by the wild-type hemophilia A gene. Factor VIIIis needed to form blood clots. Thus, factor VIII is rapidly destroyed in the absence of vWF.Which of the following might successfully be employed in the treatment of bleeding episodes in hemophiliac patients? Would the treatments workimmediately or only after some delay needed forprotein synthesis? Would the treatments have only ashort-term or a prolonged effect? Assume that allmutations are null (that is, the mutations result in thecomplete absence of the protein encoded by the gene)and that the plasma is cell-free.a. transfusion of plasma from normal blood into avWD patientb. transfusion of plasma from a vWD patient into adifferent vWD patientc. transfusion of plasma from a hemophilia A…
An acute leukemia patient presents with blast morphology that is of neutrophil lineage with Auer rods and pseudo−Pelger-Huët nuclei, myeloperoxidase, and Sudan Black B. Cytogenetic analysis reveals a t(8;21)(q22;q22) translocation in the majority of the blasts. Which classification of AML best fits this morphology, immunophenotyping, and cytochemistry? Select one: a.AML with recurrent genetic abnormalities b.AML with multilineage dysplasia c.AML, therapy-related d.AML not otherwise categorized
The extensive polymorphism of MHC genes in the population is thought to represent an evolutionary response to outflank the evasive strategies of pathogens. This polymorphism makes it difficult for pathogens to eliminate all potential MHC binding epitopes from their proteins. Based on this reasoning, it would seem advantageous for each individual to encode more than three different MHC class I and three different MHC class II genes per chromosome copy. If some individuals in the population had MHC loci that encoded 10 different MHC class I and 10 different MHC class II genes, the T cell repertoire in those individuals would likely be: Much more diverse than in the rest of the individuals of that population Much better at recognizing rare pathogens not encountered by most individuals in that population Much less diverse than the rest of the individuals in that population Much more alloreactive than the T cells found in the other individuals of that population Very reactive to bacterial…
Knowledge Booster
Background pattern image
Biology
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
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Biology: The Unity and Diversity of Life (MindTap...
Biology
ISBN:9781305073951
Author:Cecie Starr, Ralph Taggart, Christine Evers, Lisa Starr
Publisher:Cengage Learning
Text book image
Human Heredity: Principles and Issues (MindTap Co...
Biology
ISBN:9781305251052
Author:Michael Cummings
Publisher:Cengage Learning