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23 Jan 2019

Describe how each of the following ways generate antibody diversity in B cells.

At the level of DNA:

a) VDJ recombination

b) Class switch recombination

c) Somatic hypermutation

At the level of RNA:

d) mRNA splicing

e) Receptor/secretion

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24 Jan 2019

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Question XIII. One of the aspects by which memory Bcells active in a secondary immune response differ from the naiveB-cell population activated in a primary immune response isthat
[complete the sentence and assess each subsequent statement(108-114) as either factually correct (= “true”) or incorrect (=“false”)]:
108. the frequency of antigen-specific B cells is lower in asecondary immune response.

109. the antibody produced is of higher affinity in a secondaryimmune response.
110. the level of somatic hypermutation is higher in a secondaryimmune response.

111. higher levels of IgM are produced in secondary immuneresponses.
112. B cells do not require T-cell help in secondary immuneresponses.
113. memory B cells express higher levels of MHC class IImolecules.
114. naive B cells express higher levels of co-stimulatorymolecules.

1. What reaction is catalyzed by reverse transcriptase and used in the laboratory to generate cDNA?

a. transcription of RNA to DNA

b. transcription of DNA to RNA

c. conversion of ribonucleotides into deoxyribonucleotides

d. translation of RNA to DNA

e. conversion of a ribonucleotide to a DNA double helix

2. In eukaryotic cells, _________determine the amount of mRNA arising from a particular gene.

a. transcriptional-level controls

b. RNA processing-level controls

c. translational-level controls

d. replication-level controls

e. b and c

3. In eukaryotic cells, _________determine how a primary transcript is converted to mature mRNA

a. transcriptional-level controls

b. RNA processing-level controls

c. translational-level controls

d. replication-level controls

e. a and d

4. In eukaryotic cells, _________determine when a particular mRNA is actually used in protein synthesis.

a. transcriptional-level controls

b. RNA processing-level controls

c. translational-level controls

d. replication-level controls

e. None of the above because protein synthesis takes place immediately

5. Under what circumstances do cells selectively activate and suppress their genes?

a. at different stages of embryonic development

b. in different tissues

c. exposure to different types of stimuli

d. No such circumstances exist in nature—cells express all their genes throughout life.

e. a, b and c

6. Which statement about the control of gene expression is FALSE?

a. A single gene may be controlled by different transcription factors.

b. A single transcription factor may be necessary for the expression of different genes.

c. Each cell type has a characteristic pattern of gene transcription, which is determined by the particular complement of transcription factors contained in that cell.

d. Expression of protein genes is primarily controlled in nucleoli

e. Control of gene transcription is complex and influenced by various circumstances.

7. What is thought to maintain X chromosome inactivation in females?

a. DNA acetylation

b. DNA methylation

c. RNA inactivation

d. Histone methylation

e. None of the above because both X chromosomes are active in females and males.

1. It is well documented that antibody affinities for an immunizing antigen continue to increase upon successive rounds of immunization (i.e., secondary, tertiary, etc.). This is due to the fact that:
A. At each round of immunization, new naive B cells are recruited into the response.
B. At each round of immunization, the expression of AID increases, leading to higher rates of somatic hypermutation.
C. Memory B cells express higher levels of AID than naive B cells, leading to higher rates of somatic hypermutation.
D. Memory B cells can re-enter germinal centers and undergo
additional somatic hypermutation.
E. At each round of immunization, germinal centers become larger
and have increased numbers of B cells in them.

2. The US Department of Health and Human Services has a stated goal for the seasonal influenza vaccine of vaccinating 80% of healthy (i.e., low-risk) individuals. This vaccine is formulated each year from the serotypes of influenza likely to be circulating in the population during the coming flu season. The reason this goal is not 100% of individuals is because:
A. It is not feasible to expect 100% of healthy individuals to get the flu vaccine every year.
B. Individuals who had the flu vaccine the year before will already be protected.
C. Individuals who are healthy need not be too concerned about getting infected with flu.
D. Healthy individuals are unlikely to spread the virus to others.
E. Unvaccinated individuals are protected when 80% of people
around them are vaccinated.

3. Most vaccines currently administered are delivered by intramuscular injection. Yet the pathogenic organisms these vaccines aim to protect against usually enter the body by a different route. For instance, many viruses infect us via the respiratory tract, and many bacterial pathogens infect via the gastrointestinal tract. One major advantage of delivering vaccines against these organisms via their normal route of infection would be:
A. That the vaccines would no longer require the incorporation of an adjuvant in their composition
B. That the vaccines would elicit IgA antibodies in addition to IgG antibodies
C. That the vaccines would no longer require several boosters to elicit protective responses
D. That the vaccines would be more stable and not require refrigeration
E. That the vaccines would be safer and have fewer side effects than
injected vaccines

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