Campbell Biology in Focus (2nd Edition)
2nd Edition
ISBN: 9780321962751
Author: Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky, Jane B. Reece
Publisher: PEARSON
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Chapter 35, Problem 12TYU
Summary Introduction
To determine:
The reason for the loss of DNA in mature B and T cells, focusing primarily on the similarities between cellular and organismal generations.
Introduction:
T cells and the B cells are the cells that provide cellular immunity to the body. These cells posses the receptors or the antibodies that recognize a foreign antigen. This process in turn elicits the immune response of the body.
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Bacteriophage is added to a culture of human T cells and none of the human T cells were infected by bacteriophage. Why?
T cells do not have the proper protein machinery to carry out transcription and translation of bacteriophage genes.
T cells do not have the corresponding cell surface receptors that are recognized by bacteriophage viruses.
T cells have a thick outer cell wall that blocks bacteriophage infection.
T cells do not carry out DNA replication and thus are not good hosts for the bacteriophage viruses.
Would it be effective to use an inhibitor of RNA polymerase to block the HIV replication cycle and subsequent infection of human T cells?
Yes, this would stop the transcription of viral genes and prevent HIV from being able to replicate.
No, these types of inhibitors do not exist and would be impossible to make.
No, this would block transcription of T cell genes, leading to the death of T cells and compromised immune systems in individuals.
Yes, inhibitors of RNA polymerase are easy and relatively inexpensive to produce and make good therapeutics.
B cells are specialized blood cells that secrete antibodies. Normally, human blood has millions of differenttypes of B cells making millions of different kinds ofantibody molecules. This variety occurs because, as described in the Fast Forward Box in Chapter 13 entitledProgrammed DNA Rearrangements and the ImmuneSystem, antibody genes undergo rearrangements in theprecursors of B cells. Individual B cell precursorsrearrange their antibody genes in different ways.In the blood of patients with cancers called B celllymphomas, almost all of the antibody molecules areall of one type, but this single type of antibody isdifferent in different lymphoma patients.a. Based on this information, provide a brief description of the genesis of B cell lymphomas, focusingon the cells that are overproliferating.
Chapter 35 Solutions
Campbell Biology in Focus (2nd Edition)
Ch. 35.1 - Pus is both a sign of infection and an indicator...Ch. 35.1 - MAKE CONNECTIONS How do the molecules that...Ch. 35.1 - Prob. 3CCCh. 35.2 - Prob. 1CCCh. 35.2 - Explain how memory cells strengthen the immune...Ch. 35.2 - WHAT IF? If both copies of a light-chain gene and...Ch. 35.3 - Prob. 1CCCh. 35.3 - Prob. 2CCCh. 35.3 - Prob. 3CCCh. 35 - Prob. 1TYU
Ch. 35 - Prob. 2TYUCh. 35 - Prob. 3TYUCh. 35 - Prob. 4TYUCh. 35 - Prob. 5TYUCh. 35 - Prob. 6TYUCh. 35 - Prob. 7TYUCh. 35 - DRAW IT Consider a pencil-shaped protein with two...Ch. 35 - MAKE CONNECTIONS Contrast clonal selection with...Ch. 35 - Prob. 10TYUCh. 35 - FOCUS ON EVOLUTION Describe one invertebrate...Ch. 35 - Prob. 12TYUCh. 35 - Prob. 13TYU
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- Researchers can make monoclonal antibodies by immunizing a mouse with a molecule (or with a microorganism). The resulting antibody-mediated response produces a set of antibodies that recognize different parts of the molecule. The mouse's B cells are then harvested from its spleen and fused with cancerous B cells from a myeloma cell line. The resulting hybrid myeloma ("hybridoma") cells are cloned: Individual cells are grown in tissue culture as separate cell lines. Each cell line produces and secretes antibodies that recognize one part of the immunizing molecule. These antibodies are called monoclonal antibodies, and they can be purified and used for research or other purposes. Monoclonal antibodies are effective for passive immunization, but only in the immediate term. Antibodies produced by one's own immune system can last up to about six months in the bloodstream, but monoclonals delivered in passive immunization often last for less than a week. Why the difference?arrow_forwardThe Adaptive Immune Response Is a Specific Defense Against Infection In cystic fibrosis gene therapy, scientists propose the use of viral vectors to deliver normal genes to cells in the lungs. What immunological risks are involved in this procedure?arrow_forwardThe Adaptive Immune Response Is a Specific Defense Against Infection Describe the genetic basis of antibody diversity.arrow_forward
- What does innate mean? How is the innate immune system different from the adaptive immune system? Compare the strategies of innate immunity with strategies of adaptive immunity. Give specific examples. How do vaccines protect us from diseases? Which cells in the immune system become activated after the injection? Your answer should be written as 2 or more paragraphs with a total word count of 400 or more.arrow_forwardusing a molecular genetic approach how can one generate a mouse missing an adaptive immune responsearrow_forwardAtaxia-telangiectasis (ATM) is a rare genetic neurodegenerative disease. About 20% of people with ATM develop acute lymphocytic leukemia or lymphoma, cancers of the immune-system cells. Cells in many of these cancers exhibit chromosome rearrangements, with chromosome breaks occurring at antibody and T-cell-receptor genes (A. L. Bredemeyer et al. 2006. Nature 442:466–470). Many people with ATM also have a weakened immune system, which makes them susceptible to respiratory infections. Research has shown that the locus that causes ATM has a role in the repair of double-strand breaks. Explain why people who have a genetic defect in the repair of doublestrand breaks might have a high incidence of chromosome rearrangements in their immune-system cells and why their immune systems might be weakened.arrow_forward
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