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Chapter 2 The Central Dogma: Exploring Genetic Disease

Chapter 2 The Central Dogma: Exploring Genetic Disease

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Page 1: Chapter 2 The Central Dogma: Exploring Genetic Disease

Chapter 2The Central Dogma: Exploring

Genetic Disease

Page 2: Chapter 2 The Central Dogma: Exploring Genetic Disease

Figure 2.1: “Sickled” red blood cells

© Eye of Science/Photo Researchers, Inc.

Page 3: Chapter 2 The Central Dogma: Exploring Genetic Disease

Figure 2.2: The hemoglobin molecule

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Figure 2.3: An individual has two copies of each gene: the same (homozygous) or different (heterozygous)

Page 5: Chapter 2 The Central Dogma: Exploring Genetic Disease

Figure 2.4: Four possible outcomes for the child of two carriers of the sickle-cell trait. W=wild-type allele; S=sickle-cell allele

Page 6: Chapter 2 The Central Dogma: Exploring Genetic Disease

Figure 2.5: A DNA molecule is made up of two strands of nucleotides

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Figure 2.6: Synthesis of RNA, a single-stranded molecule complementary to one of the two DNA strands

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Figure 2.T1: The Genetic Code

Page 9: Chapter 2 The Central Dogma: Exploring Genetic Disease

Figure 2.7: Diagram showing how a single gene encoded in DNA is transcribed and translated to produce a protein

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Figure 2.8: The human HBB gene in FASTA format

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Figure 2.9: A vest designed to improve lung function for cystic fibrosis patients

© 2008 Hill-Rom Services, Inc., Reprinted with Permission-All rights Reserved.

Page 12: Chapter 2 The Central Dogma: Exploring Genetic Disease

Figure 2.10: Schematic diagram showing the structure of the CFTR protein that regulates transport of chloride through cell membranes