Concepts of Genetics (12th Edition)
Concepts of Genetics (12th Edition)
12th Edition
ISBN: 9780134604718
Author: William S. Klug, Michael R. Cummings, Charlotte A. Spencer, Michael A. Palladino, Darrell Killian
Publisher: PEARSON
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Chapter 13, Problem 1CS
Summary Introduction

To determine: The way in which mutation in hemoglobin β affects promoter, enhancer, and coding regions of the gene encoding hemoglobin β.

Introduction: The mutation in a β-hemoglobin gene can result in occurrence β thalassemia. β -thalassemia is a recessive trait that affects the oxygen-carrying capacity of the red blood cells (RBCs). This destroys RBCs and causes the availability of a huge amount of iron in the body. The iron starts depositing in the tissues and organs.

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Given that a faulty ribosomal protein is the culprit and causes DBA, discuss the possible role of normal ribosomal proteins. Why might bone marrow cells be more susceptible to such a mutation than other cells?
What type of mutation is sickle cell anemia? Explain the molecular basis of sickle cell anemia.
A gene contains the sequence CGCATACGGTAC that results in the amino acid sequence arg-ile-arq- tyr. A mutation in this gene has a G inserted after the second C in the strand. How will this mutation affect the phenotype? A)This will affect the phenotype because although most of the protein will be identical, the first amino acid will be different. B)This will not affect the phenotype because only the second amino acid is different from the original protein. C)This will not affect the phenotype because the protein will be identical to the original protein. D)This will affect the phenotype because all of the amino acids after the first one will be different from the original protein.

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Concepts of Genetics (12th Edition)

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