Description
Efnisyfirlit
- Title Page
- Copyright
- About The Authors
- Detailed Contents
- Preface
- Acknowledgments
- Chapter 1. A Preview of Cell Biology
- 1.1 The Cell Theory: A Brief History
- Advances in Microscopy Allowed Detailed Studies of Cells
- The Cell Theory Applies to All Organisms
- 1.2 The Emergence of Modern Cell Biology
- The Cytological Strand Deals with Cellular Structure
- The Biochemical Strand Concerns the Chemistry of Biological Structure and Function
- The Genetic Strand Focuses on Information Flow
- 1.3 How Do We Know What We Know?
- Biological “Facts” May Turn Out to Be Incorrect
- Experiments Test Specific Hypotheses
- Model Organisms Play a Key Role in Modern Cell Biology Research
- Well-Designed Experiments Alter Only One Variable at a Time
- Summary of Key Points
- Problem Set
- Key Technique: Using Immunofluorescence to Identify Specific Cell Components
- Human Connections: The Immortal Cells of Henrietta Lacks
- Chapter 2. The Chemistry of the Cell
- 2.1 The Importance of Carbon
- Carbon-Containing Molecules Are Stable
- Carbon-Containing Molecules Are Diverse
- Carbon-Containing Molecules Can Form Stereoisomers
- 2.2 The Importance of Water
- Water Molecules Are Polar
- Water Molecules Are Cohesive
- Water Has a High Temperature-Stabilizing Capacity
- Water Is an Excellent Solvent
- 2.3 The Importance of Selectively Permeable Membranes
- A Membrane Is a Lipid Bilayer with Proteins Embedded in It
- Lipid Bilayers Are Selectively Permeable
- 2.4 The Importance of Synthesis by Polymerization
- Macromolecules Are Critical for Cellular Form and Function
- Cells Contain Three Different Kinds of Macromolecular Polymers
- Macromolecules Are Synthesized by Stepwise Polymerization of Monomers
- 2.5 The Importance of Self-Assembly
- Noncovalent Bonds and Interactions Are Important in the Folding of Macromolecules
- Many Proteins Spontaneously Fold into Their Biologically Functional State
- Molecular Chaperones Assist the Assembly of Some Proteins
- Self-Assembly Also Occurs in Other Cellular Structures
- The Tobacco Mosaic Virus Is a Case Study in Self-Assembly
- Self-Assembly Has Limits
- Hierarchical Assembly Provides Advantages for the Cell
- Summary of Key Points
- Problem Set
- Key Technique: Determining the Chemical Fingerprint of a Cell Using Mass Spectrometry
- Human Connections: Taking a Deeper Look: Magnetic Resonance Imaging (MRI)
- Chapter 3. The Macromolecules of the Cell
- 3.1 Proteins
- The Monomers Are Amino Acids
- The Polymers Are Polypeptides and Proteins
- Several Kinds of Bonds and Interactions Are Important in Protein Folding and Stability
- Protein Structure Depends on Amino Acid Sequence and Interactions
- 3.2 Nucleic Acids
- The Monomers Are Nucleotides
- The Polymers Are DNA and RNA
- A DNA Molecule Is a Double-Stranded Helix
- 3.3 Polysaccharides
- The Monomers Are Monosaccharides
- The Polymers Are Storage and Structural Polysaccharides
- Polysaccharide Structure Depends on the Kinds of Glycosidic Bonds Involved
- 3.4 Lipids
- Fatty Acids Are the Building Blocks of Several Classes of Lipids
- Triacylglycerols Are Storage Lipids
- Phospholipids Are Important in Membrane Structure
- Glycolipids Are Specialized Membrane Components
- Steroids Are Lipids with a Variety of Functions
- Terpenes Are Formed from Isoprene
- Summary of Key Points
- Problem Set
- Human Connections: Aggregated Proteins and Alzheimer’s
- Key Technique: Using X-Ray Crystallography to Determine Protein Structure
- Chapter 4. Cells and Organelles
- 4.1 The Origins of the First Cells
- Simple Organic Molecules May Have Formed Abiotically in the Young Earth
- RNA May Have Been the First Informational Molecule
- Liposomes May Have Defined the First Primitive Protocells
- 4.2 Basic Properties of Cells
- The Three Domains of Life Are Bacteria, Archaea, and Eukaryotes
- There Are Several Limitations on Cell Size
- Bacteria, Archaea, and Eukaryotes Differ from Each Other in Many Ways
- 4.3 The Eukaryotic Cell in Overview: Structure and Function
- The Plasma Membrane Defines Cell Boundaries and Retains Contents
- The Nucleus Is the Information Center of the Eukaryotic Cell
- Mitochondria and Chloroplasts Provide Energy for the Cell
- The Endosymbiont Theory Proposes That Mitochondria and Chloroplasts Were Derived from Bacteria
- The Endomembrane System Synthesizes Proteins for a Variety of Cellular Destinations
- Other Organelles Also Have Specific Functions
- Ribosomes Synthesize Proteins in the Cytoplasm
- The Cytoskeleton Provides Structure to the Cytoplasm
- The Extracellular Matrix and Cell Walls Are Outside the Plasma Membrane
- 4.4 Viruses, Viroids, and Prions: Agents That Invade Cells
- A Virus Consists of a DNA or RNA Core Surrounded by a Protein Coat
- Viroids Are Small, Circular RNA Molecules That Can Cause Plant Diseases
- Prions Are Infectious Protein Molecules
- Summary of Key Points
- Problem Set
- Human Connections: When Cellular “Breakdown” Breaks Down
- Key Technique: Using Centrifugation to Isolate Organelles
- Chapter 5. Bioenergetics: The Flow of Energy in the Cell
- 5.1 The Importance of Energy
- Cells Need Energy to Perform Six Different Kinds of Work
- Organisms Obtain Energy Either from Sunlight or from the Oxidation of Chemical Compounds
- Energy Flows Through the Biosphere Continuously
- The Flow of Energy Through the Biosphere Is Accompanied by a Flow of Matter
- 5.2 Bioenergetics
- Understanding Energy Flow Requires Knowledge of Systems, Heat, and Work
- The First Law of Thermodynamics States That Energy Is Conserved
- The Second Law of Thermodynamics States That Reactions Have Directionality
- Entropy and Free Energy Are Two Means of Assessing Thermodynamic Spontaneity
- 5.3 Understanding ΔG and Keq
- The Equilibrium Constant Keq Is a Measure of Directionality
- ΔG Can Be Calculated Readily
- The Standard Free Energy Change Is ΔG Measured Under Standard Conditions
- Summing Up: The Meaning of ΔGʹ and ΔG°ʹ
- Free Energy Change: Sample Calculations
- Jumping Beans Provide a Useful Analogy for Bioenergetics
- Life Requires Steady-State Reactions That Move Toward Equilibrium Without Ever Getting There
- Summary of Key Points
- Problem Set
- Human Connections: The “Potential” of Food to Provide Energy
- Key Technique: Measuring How Molecules Bind to One Another Using Isothermal Titration Calorimetry
- Chapter 6. Enzymes: The Catalysts of Life
- 6.1 Activation Energy and the Metastable State
- Before a Chemical Reaction Can Occur, the Activation Energy Barrier Must Be Overcome
- The Metastable State Is a Result of the Activation Barrier
- Catalysts Overcome the Activation Energy Barrier
- 6.2 Enzymes as Biological Catalysts
- Most Enzymes Are Proteins
- Substrate Binding, Activation, and Catalysis Occur at the Active Site
- Ribozymes Are Catalytic RNA Molecules
- 6.3 Enzyme Kinetics
- Monkeys and Peanuts Provide a Useful Analogy for Understanding Enzyme Kinetics
- Most Enzymes Display Michaelis–Menten Kinetics
- What Is the Meaning of V max and Km?
- Why Are Km and Vmax Important to Cell Biologists?
- The Double-Reciprocal Plot Is a Useful Means of Visualizing Kinetic Data
- Enzyme Inhibitors Act Either Irreversibly or Reversibly
- 6.4 Enzyme Regulation
- Allosteric Enzymes Are Regulated by Molecules Other than Reactants and Products
- Allosteric Enzymes Exhibit Cooperative Interactions Between Subunits
- Enzymes Can Also Be Regulated by the Addition or Removal of Chemical Groups
- Summary of Key Points
- Problem Set
- Human Connections: Ace Inhibitors: Enzyme Activity as TheDifference Between Life and Death
- Key Technique: Determining Km and Vmax Using Enzyme Assays
- Chapter 7. Membranes: Their Structure, Function, and Chemistry
- 7.1 The Functions of Membranes
- Membranes Define Boundaries and Serve as Permeability Barriers
- Membranes Contain Specific Proteins and Therefore Have Specific Functions
- Membrane Proteins Regulate the Transport of Solutes
- Membrane Proteins Detect and Transmit Electrical and Chemical Signals
- Membrane Proteins Mediate Cell Adhesion and Cell-to-Cell Communication
- 7.2 Models of Membrane Structure: An Experimental Perspective
- Overton and Langmuir: Lipids Are Important Components of Membranes
- Gorter and Grendel: The Basis of Membrane Structure Is a Lipid Bilayer
- Davson and Danielli: Membranes Also Contain Proteins
- Robertson: All Membranes Share a Common Underlying Structure
- Further Research Revealed Major Shortcomings of the Davson–Danielli Model
- Singer and Nicolson: A Membrane Consists of a Mosaic of Proteins in a Fluid Lipid Bilayer
- Unwin and Henderson: Most Membrane Proteins Contain Transmembrane Segments
- 7.3 Membrane Lipids: The “Fluid” Part of the Model
- Membranes Contain Several Major Classes of Lipids
- Fatty Acids Are Essential to Membrane Structure and Function
- Thin-Layer Chromatography Is an Important Technique for Lipid Analysis
- Membrane Asymmetry: Most Lipids Are Distributed Unequally Between the Two Monolayers
- The Lipid Bilayer Is Fluid
- Most Organisms Can Regulate Membrane Fluidity
- Lipid Micro- or Nanodomains May Localize Molecules in Membranes
- 7.4 Membrane Proteins: The “Mosaic” Part of the Model
- The Membrane Consists of a Mosaic of Proteins: Evidence from Freeze-Fracture Microscopy
- Membranes Contain Integral, Peripheral, and Lipid-Anchored Proteins
- Membrane Proteins Can Be Isolated and Analyzed
- Determining the Three-Dimensional Structure of Membrane Proteins Is Becoming Easier
- Molecular Biology Has Contributed Greatly to Our Understanding of Membrane Proteins
- Membrane Proteins Have a Variety of Functions
- Membrane Proteins Are Oriented Asymmetrically Across the Lipid Bilayer
- Many Membrane Proteins and Lipids Are Glycosylated
- Membrane Proteins Vary in Their Mobility
- The Erythrocyte Membrane Contains an Interconnected Network of Membrane-Associated Proteins
- Summary of Key Points
- Problem Set
- Key Technique: Fluorescence Recovery After Photobleaching (FRAP)
- Human Connections: It’s All in the Family
- Chapter 8. Transport Across Membranes: Overcoming the Permeability Barrier
- 8.1 Cells and Transport Processes
- Solutes Cross Membranes by Simple Diffusion, Facilitated Diffusion, and Active Transport
- The Movement of a Solute Across a Membrane Is Determined by Its Concentration Gradient or Its Electr
- The Erythrocyte Plasma Membrane Provides Examples of Transport
- 8.2 Simple Diffusion: Unassisted Movement Down the Gradient
- Simple Diffusion Always Moves Solutes Toward Equilibrium
- Osmosis Is the Simple Diffusion of Water Across a Selectively Permeable Membrane
- Simple Diffusion Is Typically Limited to Small, Uncharged Molecules
- The Rate of Simple Diffusion Is Directly Proportional to the Concentration Gradient
- 8.3 Facilitated Diffusion: Protein-Mediated Movement Down the Gradient
- Carrier Proteins and Channel Proteins Facilitate Diffusion by Different Mechanisms
- Carrier Proteins Alternate Between Two Conformational States
- Carrier Proteins Are Analogous to Enzymes in Their Specificity and Kinetics
- Carrier Proteins Transport Either One or Two Solutes
- The Erythrocyte Glucose Transporter and Anion Exchange Protein Are Examples of Carrier Proteins
- Channel Proteins Facilitate Diffusion by Forming Hydrophilic Transmembrane Channels
- 8.4 Active Transport: Protein-Mediated Movement Up the Gradient
- The Coupling of Active Transport to an Energy Source May Be Direct or Indirect
- Direct Active Transport Depends on Four Types of Transport ATPases
- Indirect Active Transport Is Driven by Ion Gradients
- 8.5 Examples of Active Transport
- Direct Active Transport: The Na+/K+ Pump Maintains Electrochemical Ion Gradients
- Indirect Active Transport: Sodium Symport Drives the Uptake of Glucose
- The Bacteriorhodopsin Proton Pump Uses Light Energy to Transport Protons
- 8.6 The Energetics of Transport
- For Uncharged Solutes, the ΔG of Transport Depends Only on the Concentration Gradient
- For Charged Solutes, the ΔG of Transport Depends on the Electrochemical Potential
- Summary of Key Points
- Problem Set
- Key Technique: Expression of Heterologous Membrane Proteins in Frog Oocytes
- Human Connections: Membrane Transport, Cystic Fibrosis, and the Prospects for Gene Therapy
- Chapter 9. Chemotrophic Energy Metabolism: Glycolysis and Fermentation
- 9.1 Metabolic Pathways
- 9.2 ATP: The Primary Energy Molecule in Cells
- ATP Contains Two Energy-Rich Phosphoanhydride Bonds
- ATP Hydrolysis Is Exergonic Due to Several Factors
- ATP Is Extremely Important in Cellular Energy Metabolism
- 9.3 Chemotrophic Energy Metabolism
- Biological Oxidations Usually Involve the Removal of Both Electrons and Protons and Are Exergonic
- Coenzymes Such as NAD+ Serve as Electron Acceptors in Biological Oxidations
- Most Chemotrophs Meet Their Energy Needs by Oxidizing Organic Food Molecules
- Glucose Is One of the Most Important Oxidizable Substrates in Energy Metabolism
- The Oxidation of Glucose Is Highly Exergonic
- Glucose Catabolism Yields Much More Energy in the Presence of Oxygen Than in Its Absence
- Based on Their Need for Oxygen, Organisms Are Aerobic, Anaerobic, or Facultative
- 9.4 Glycolysis: ATP Generation Without the Involvement of Oxygen
- Glycolysis Generates ATP by Catabolizing Glucose to Pyruvate
- 9.5 Fermentation
- In the Absence of Oxygen, Pyruvate Undergoes Fermentation to Regenerate NAD+
- Fermentation Taps Only a Fraction of the Substrate’s Free Energy but Conserves That Energy Efficie
- Cancer Cells Ferment Glucose to Lactate Even in the Presence of Oxygen
- 9.6 Alternative Substrates for Glycolysis
- Other Sugars and Glycerol Are Also Catabolized by the Glycolytic Pathway
- Polysaccharides Are Cleaved to Form Sugar Phosphates That Also Enter the Glycolytic Pathway
- 9.7 Gluconeogenesis
- 9.8 The Regulation of Glycolysis and Gluconeogenesis
- Key Enzymes in the Glycolytic and Gluconeogenic Pathways Are Subject to Allosteric Regulation
- Fructose-2,6-Bisphosphate Is an Important Regulator of Glycolysis and Gluconeogenesis
- Glycolytic Enzymes May Have Functions Beyond Glycolysis
- Summary of Key Points
- Problem Set
- Key Technique: Using Isotopic Labeling to Determine the Fate of Atoms in a Metabolic Pathway
- Human Connections: What Happens to the Sugar?
- Chapter 10. Chemotrophic Energy Metabolism: Aerobic Respiration
- 10.1 Cellular Respiration: Maximizing ATP Yields
- Aerobic Respiration Yields Much More Energy than Fermentation Does
- Respiration Includes Glycolysis, Pyruvate Oxidation, the Citric Acid Cycle, Electron Transport, and
- 10.2 The Mitochondrion: Where the Action Takes Place
- Mitochondria Are Often Present Where the ATP Needs Are Greatest
- Mitochondria Can Adopt Complex Shapes and Vary in Number in Different Cell Types
- The Outer and Inner Membranes Define Two Separate Mitochondrial Compartments and Three Regions
- Many Mitochondrial Proteins Originate in the Cytosol
- Mitochondrial Functions Occur in or on Specific Membranes and Compartments
- In Bacteria, Respiratory Functions Are Localized to the Plasma Membrane and the Cytoplasm
- 10.3 The Citric Acid Cycle: Oxidation in the Round
- Pyruvate Is Converted to Acetyl Coenzyme A by Oxidative Decarboxylation
- The Citric Acid Cycle Begins with the Entry of Two Carbons from Acetyl CoA
- Two Oxidative Decarboxylations Then Form NADH and Release CO2
- Direct Generation of GTP (or ATP) Occurs at One Step in the Citric Acid Cycle
- The Final Oxidative Reactions of the Citric Acid Cycle Generate FADH2 and NADH
- Summing Up: The Products of the Citric Acid Cycle Are CO2 , ATP, NADH, and FADH2
- Several Citric Acid Cycle Enzymes Are Subject to Allosteric Regulation
- The Citric Acid Cycle Also Plays a Central Role in the Catabolism of Fats and Proteins
- The Citric Acid Cycle Serves as a Source of Precursors for Anabolic Pathways
- The Glyoxylate Cycle Converts Acetyl CoA to Carbohydrates in Plants
- 10.4 Electron Transport: Electron Flow from Coenzymes to Oxygen
- The Electron Transport Chain Conveys Electrons from Reduced Coenzymes to Oxygen
- The Electron Transport Chain Consists of Five Kinds of Carriers
- The Electron Carriers Function in a Sequence Determined by Their Reduction Potentials
- Most of the Carriers Are Organized into Four Large Respiratory Complexes
- The Respiratory Complexes Move Freely Within the Inner Membrane
- 10.5 The Electrochemical Proton Gradient: Key to Energy Coupling
- Electron Transport and ATP Synthesis Are Coupled Events
- Coenzyme Oxidation Pumps Enough Protons to Form Three ATP Moleculesper NADH and Two ATP Molecules pe
- The Chemiosmotic Model Is Affirmed by an Impressive Array of Evidence
- 10.6 ATP Synthesis: Putting It All Together
- F1 Particles Have ATP Synthase Activity
- Proton Translocation Through Fo Drives ATP Synthesis by F1
- ATP Synthesis by FoF1 Involves Physical Rotation of the Gamma Subunit
- 10.7 Aerobic Respiration: Summing It All Up
- The Actual ATP Yield per Glucose during Aerobic Respiration Is Influencedby Several Factors
- Aerobic Respiration: A Remarkable Process
- Summary of Key Points
- Problem Set
- Key Technique: Visualizing Cellular Structures with Three-Dimensional Electron Microscopy
- Human Connections: A Diet Worth Dying For?
- Chapter 11. Phototrophic Energy Metabolism: Photosynthesis
- 11.1 An Overview of Photosynthesis
- The Energy Transduction Reactions Convert Solar Energy to Chemical Energy
- The Carbon Assimilation Reactions Fix Carbon by Reducing Carbon Dioxide
- The Chloroplast Is the Photosynthetic Organelle in Eukaryotic Cells
- Chloroplasts Are Composed of Three Membrane Systems
- 11.2 Photosynthetic Energy Transduction I: Light Harvesting
- Chlorophyll Is Life’s Primary Link to Sunlight
- Accessory Pigments Further Expand Access to Solar Energy
- Light-Gathering Molecules Are Organized into Photosystems and Light-Harvesting Complexes
- Oxygenic Phototrophs Have Two Types of Photosystems
- 11.3 Photosynthetic Energy Transduction II: NADPH Synthesis
- Photosystem II Transfers Electrons from Water to a Plastoquinone
- The Cytochrome b6/f Complex Transfers Electrons from a Plastoquinol to Plastocyanin
- Photosystem I Transfers Electrons from Plastocyanin to Ferredoxin
- Ferredoxin-NADP+ Reductase Catalyzes the Reduction of NADP+
- 11.4 Photosynthetic Energy Transduction III: ATP Synthesis
- A Chloroplast ATP Synthase Couples Transport of Protons Across the Thylakoid Membrane to ATP Synthes
- Cyclic Photophosphorylation Allows a Photosynthetic Cell to Balance NADPH and ATP Synthesis
- A Summary of the Complete Energy Transduction System
- Bacteria Use a Photosynthetic Reaction Center and Electron Transport System Similar to Those in Plan
- 11.5 Photosynthetic Carbon Assimilation I: The Calvin Cycle
- Carbon Dioxide Enters the Calvin Cycle by Carboxylation of Ribulose-1,5-Bisphosphate
- 3-Phosphoglycerate Is Reduced to Form Glyceraldehyde-3-Phosphate
- Regeneration of Ribulose-1,5-Bisphosphate Allows Continuous Carbon Assimilation
- The Complete Calvin Cycle and Its Relation to Photosynthetic Energy Transduction
- 11.6 Regulation of the Calvin Cycle
- The Calvin Cycle Is Highly Regulated to Ensure Maximum Efficiency
- Rubisco Activase Regulates Carbon Fixation by Rubisco
- 11.7 Photosynthetic Carbon Assimilation II: Carbohydrate Synthesis
- Glucose-1-Phosphate Is Synthesized from Triose Phosphates
- Biosynthesis of Sucrose Occurs in the Cytosol
- Biosynthesis of Starch Occurs in the Chloroplast Stroma
- Photosynthesis Also Produces Reduced Nitrogen and Sulfur Compounds
- 11.8 Rubisco’s Oxygenase Activity Decreases Photosynthetic Efficiency
- The Glycolate Pathway Returns Reduced Carbon from Phosphoglycolate to the Calvin Cycle
- C4 Plants Minimize Photorespiration by Confining Rubisco to CellsContaining High Concentrations of C
- CAM Plants Minimize Photorespiration and Water Loss by Opening Their Stomata Only at Night
- Summary of Key Points
- Problem Set
- Key Technique: Determining Absorption and Action Spectra via Spectrophotometry
- Human Connections: How Do Plants Put On Sunscreen?
- Chapter 12. The Endomembrane System and Protein Sorting
- 12.1 The Endoplasmic Reticulum
- The Two Basic Kinds of Endoplasmic Reticulum Differ in Structure and Function
- Rough ER Is Involved in the Biosynthesis and Processing of Proteins
- Smooth ER Is Involved in Drug Detoxification, Carbohydrate Metabolism, Calcium Storage, and Steroid
- The ER Plays a Central Role in the Biosynthesis of Membranes
- 12.2 The Golgi Apparatus
- The Golgi Apparatus Consists of a Series of Membrane-Bounded Cisternae
- Two Models Account for the Flow of Lipids and Proteins Through the Golgi Apparatus
- 12.3 Roles of the ER and Golgi Apparatus in Protein Processing
- Protein Folding and Quality Control Take Place Within the ER
- Initial Glycosylation Occurs in the ER
- Further Glycosylation Occurs in the Golgi Apparatus
- 12.4 Roles of the ER and Golgi Apparatus In Protein Trafficking
- Cotranslational Import Allows Some Polypeptides to Enter the ER as They Are Being Synthesized
- The Signal Recognition Particle (SRP) Attaches the Ribosome-mRNA-PolypeptideComplex to the ER Membra
- Proteins Released into the ER Lumen Are Routed to the Golgi Apparatus, Secretory Vesicles, Lysosomes
- Stop-Transfer Sequences Mediate the Insertion of Integral Membrane Proteins
- Posttranslational Import Is an Alternative Mechanism for Import into the ER Lumen
- 12.5 Exocytosis and Endocytosis: Transporting Material Across the Plasma Membrane
- Secretory Pathways Transport Molecules to the Exterior of the Cell
- Exocytosis Releases Intracellular Molecules Outside the Cell
- Endocytosis Imports Extracellular Molecules by Forming Vesicles from the Plasma Membrane
- 12.6 Coated Vesicles in Cellular Transport Processes
- Clathrin-Coated Vesicles Are Surrounded by Lattices Composed of Clathrin and Adaptor Protein
- The Assembly of Clathrin Coats Drives the Formation of Vesicles from the Plasma Membrane and TGN
- COPI- and COPII-Coated Vesicles Travel Between the ER and Golgi Apparatus Cisternae
- SNARE Proteins Mediate Fusion Between Vesicles and Target Membranes
- 12.7 Lysosomes and Cellular Digestion
- Lysosomes Isolate Digestive Enzymes from the Rest of the Cell
- Lysosomes Develop from Endosomes
- Lysosomal Enzymes Are Important for Several Different Digestive Processes
- Lysosomal Storage Diseases Are Usually Characterized by the Accumulation of Indigestible Material
- The Plant Vacuole: A Multifunctional Digestive Organelle
- 12.8 Peroxisomes
- Most Peroxisomal Functions Are Linked to Hydrogen Peroxide Metabolism
- Plant Cells Contain Types of Peroxisomes Not Found in Animal Cells
- Peroxisome Biogenesis Can Occur by Division of Preexisting Peroxisomes or by Vesicle Fusion
- Summary of Key Points
- Problem Set
- Key Technique: Visualizing Vesicles at the Cell Surface Using Total Internal Reflection (TIRF) Micro
- Human Connections: A Bad Case of the Munchies? (Autophagy In Inflammatory Bowel Disease)
- Chapter 13. Cytoskeletal Systems
- 13.1 Major Structural Elements of the Cytoskeleton
- Eukaryotes Have Three Basic Types of Cytoskeletal Elements
- Bacteria Have Cytoskeletal Systems That Are Structurally Similar to Those in Eukaryotes
- The Cytoskeleton Is Dynamically Assembled and Disassembled
- 13.2 Microtubules
- Two Types of Microtubules Are Responsible for Many Functions in the Cell
- Tubulin Heterodimers Are the Protein Building Blocks of Microtubules
- Microtubules Can Form as Singlets, Doublets, or Triplets
- Microtubules Form by the Addition of Tubulin Dimers at Their Ends
- Addition of Tubulin Dimers Occurs More Quickly at the Plus Ends of Microtubules
- Drugs Can Affect the Assembly and Stability of Microtubules
- GTP Hydrolysis Contributes to the Dynamic Instability of Microtubules
- Microtubules Originate from Microtubule-Organizing Centers Within the Cell
- MTOCs Organize and Polarize Microtubules Within Cells
- Microtubule Stability Is Tightly Regulated in Cells by a Variety of Microtubule-Binding Proteins
- 13.3 Microfilaments
- Actin Is the Protein Building Block of Microfilaments
- Different Types of Actin Are Found in Cells
- G-Actin Monomers Polymerize into F-Actin Microfilaments
- Specific Drugs Affect Polymerization of Microfilaments
- Cells Can Dynamically Assemble Actin into a Variety of Structures
- Actin-Binding Proteins Regulate the Polymerization, Length, and Organization of Microfilaments
- Proteins That Link Actin to Membranes
- Phospholipids and Rho Family GTPases Regulate Where and When Actin-Based Structures Assemble
- 13.4 Intermediate Filaments
- Intermediate Filament Proteins Are Tissue Specific
- Intermediate Filaments Assemble from Fibrous Subunits
- Intermediate Filaments Confer Mechanical Strength on Tissues
- The Cytoskeleton Is a Mechanically Integrated Structure
- Summary of Key Points
- Problem Set
- Key Technique: Studying the Dynamic Cytoskeleton
- Human Connections: When Actin Kills
- Chapter 14. Cellular Movement: Motility and Contractility
- 14.1 Microtubule-Based Movement Inside Cells: Kinesins and Dyneins
- Motor Proteins Move Cargoes Along MTs During Axonal Transport
- Classic Kinesins Move Toward the Plus Ends of Microtubules
- Kinesins Are a Large Family of Proteins
- Dyneins Are Found in Axonemes and the Cytosol
- Microtubule Motors Direct Vesicle Transport and Shape the Endomem-brane System
- 14.2 Microtubule-Based Cell Motility: Cilia And Flagella
- Cilia and Flagella Are Common Motile Appendages of Eukaryotic Cells
- Cilia and Flagella Consist of an Axoneme Connected to a Basal Body
- Doublet Sliding Within the Axoneme Causes Cilia and Flagella to Bend
- 14.3 Microfilament-Based Movement Inside Cells: Myosins
- Myosins Are a Large Family of Actin-Based Motors with Diverse Roles in Cell Motility
- Many Myosins Move Along Actin Filaments in Short Steps
- 14.4 Microfilament-Based Motility: Muscle Cells In Action
- Skeletal Muscle Cells Contain Thin and Thick Filaments
- Sarcomeres Contain Ordered Arrays of Actin, Myosin, and Accessory Proteins
- The Sliding-Filament Model Explains Muscle Contraction
- Cross-Bridges Hold Filaments Together, and ATP Powers Their Movement
- The Regulation of Muscle Contraction Depends on Calcium
- The Coordinated Contraction of Cardiac Muscle Cells Involves Electrical Coupling
- Smooth Muscle Is More Similar to Nonmuscle Cells than to Skeletal Muscle
- 14.5 Microfilament-Based Motility In Nonmuscle Cells
- Cell Migration via Lamellipodia Involves Cycles of Protrusion, Attachment, Translocation, and Detach
- Chemotaxis Is a Directional Movement in Response to a Graded Chemical Stimulus
- Amoeboid Movement Involves Cycles of Gelation and Solation of Actin
- Actin-Based Motors Move Components Within the Cytosol of Some Cells
- Summary of Key Points
- Problem Set
- Key Technique: Watching Motors Too Small to See
- Human Connections: Dyneins Help Us Tell Left From Right
- Chapter 15. Beyond the Cell: Cell Adhesions, Cell Junctions, and Extracellular Structures
- 15.1 Cell-Cell Junctions
- Adhesive Junctions Link Adjoining Cells
- Transient Cell-Cell Adhesions Are Important for Many Cellular Events
- Tight Junctions Prevent the Movement of Molecules Across Cell Layers
- Gap Junctions Allow Direct Electrical and Chemical Communication Between Cells
- 15.2 The Extracellular Matrix of Animal Cells
- Collagens Are Responsible for the Strength of the Extracellular Matrix
- Elastins Impart Elasticity and Flexibility to the Extracellular Matrix
- Collagen and Elastin Fibers Are Embedded in a Matrix of Proteoglycans
- Free Hyaluronate Lubricates Joints and Facilitates Cell Migration
- Adhesive Glycoproteins Anchor Cells to the Extracellular Matrix
- Fibronectins Bind Cells to the ECM and Foster Cellular Movement
- Laminins Bind Cells to the Basal Lamina
- Integrins Are Cell Surface Receptors That Bind ECM Components
- The Dystrophin/Dystroglycan Complex Stabilizes Attachments of Muscle Cells to the ECM
- 15.3 The Plant Cell Surface
- Cell Walls Provide a Structural Framework and Serve as a Permeability Barrier
- The Plant Cell Wall Is a Network of Cellulose Microfibrils, Polysaccharides, and Glycoproteins
- Cell Walls Are Synthesized in Several Discrete Stages
- Plasmodesmata Permit Direct Cell-Cell Communication Through the Cell Wall
- Summary of Key Points
- Problem Set
- Human Connections: The Costly Effects of Weak Adhesion
- Key Technique: Building an ECM from Scratch
- Chapter 16. The Structural Basis of Cellular Information: DNA, Chromosomes, and the Nucleus
- 16.1 Chemical Nature of the Genetic Material
- The Discovery of DNA Led to Conflicting Proposals Concerning the Chemical Nature of Genes
- Avery, MacLeod, and McCarty Showed That DNA Is the Genetic Material of Bacteria
- Hershey and Chase Showed That DNA Is the Genetic Material of Viruses
- RNA Is the Genetic Material in Some Viruses
- 16.2 DNA Structure
- Chargaff ’s Rules Reveal That A = T and G = C
- Watson and Crick Discovered That DNA Is a Double Helix
- DNA Can Be Interconverted Between Relaxed and Supercoiled Forms
- The Two Strands of a DNA Double Helix Can Be Denatured and Renatured
- 16.3 DNA Packaging
- Bacteria Package DNA in Bacterial Chromosomes and Plasmids
- Eukaryotes Package DNA in Chromatin and Chromosomes
- Nucleosomes Are the Basic Unit of Chromatin Structure
- A Histone Octamer Forms the Nucleosome Core
- Nucleosomes Are Packed Together to Form Chromatin Fibers and Chromosomes
- Changes in Histones and Chromatin Remodeling Proteins Can Alter Chromatin Packing
- Chromosomal DNA Contains Euchromatin and Heterochromatin
- Some Heterochromatin Plays a Structural Role in Chromosomes
- Chromosomes Can Be Identified by Unique Banding Patterns
- Eukaryotic Chromosomes Contain Large Amounts of Repeated DNA Sequences
- Eukaryotes Package Some of Their DNA in Mitochondria and Chloroplasts
- 16.4 The Nucleus
- A Double-Membrane Nuclear Envelope Surrounds the Nucleus
- Molecules Enter and Exit the Nucleus Through Nuclear Pores
- The Nucleus Is Mechanically Integrated with the Rest of the Cell
- Chromatin Is Located Within the Nucleus in a Nonrandom Fashion
- The Nucleolus Is Involved in Ribosome Formation
- Summary of Key Points
- Problem Set
- Key Technique: FISHing for Specific Sequences
- Human Connections: Lamins and Premature Aging
- Chapter 17. DNA Replication, Repair, and Recombination
- 17.1 DNA Replication
- DNA Synthesis Occurs During S Phase
- DNA Replication Is Semiconservative
- DNA Replication Is Usually Bidirectional
- Replication Initiates at Specialized DNA Elements
- DNA Polymerases Catalyze the Elongation of DNA Chains
- DNA Is Synthesized as Discontinuous Segments That Are Joined Together by DNA Ligase
- In Bacteria, Proofreading Is Performed by the 3’→5′ Exonuclease Activity of DNA Polymerase
- RNA Primers Initiate DNA Replication
- The DNA Double Helix Must Be Locally Unwound During Replication
- DNA Unwinding and DNA Synthesis Are Coordinated on Both Strands via the Replisome
- Eukaryotes Disassemble and Reassemble Nucleosomes as Replication Proceeds
- Telomeres Solve the DNA End-Replication Problem
- 17.2 DNA Damage and Repair
- Mutations Can Occur Spontaneously During Replication
- Mutagens Can Induce Mutations
- DNA Repair Systems Correct Many Kinds of DNA Damage
- 17.3 Homologous Recombination and Mobile Genetic Elements
- Homologous Recombination Is Initiated by Double-Strand Breaks in DNA
- Transposons Are Mobile Genetic Elements
- Transposons Differ Based on Their Autonomy and Mechanism of Movement
- Bacterial DNA-Only Transposons Can Be Composite or Noncomposite
- Eukaryotes Also Have DNA-Only Transposons
- Retrotransposons
- Summary of Key Points
- Problem Set
- Human Connections: Children of The Moon
- Key Technique: CRISPR/Cas9 Genome Editing
- Chapter 18. Gene Expression: I. Transcription
- 18.1 The Directional Flow of Genetic Information
- Transcription and Translation Involve Many of the Same Components in Prokaryotes and Eukaryotes
- Where Transcription and Translation Occur Differs in Prokaryotes and Eukaryotes
- In Some Cases RNA Is Reversed Transcribed into DNA
- 18.2 Mechanisms of Transcription
- Transcription Involves Four Stages: RNA Polymerase Binding, Initiation, Elongation, and Termination
- Bacterial Transcription Involves ˜ Factor Binding, Initiation, Elongation, and Termination
- Transcription in Eukaryotic Cells Has Additional Complexity Compared with Prokaryotes
- RNA Polymerases I, II, and III Carry Out Transcription in the Eukaryotic Nucleus
- Three Classes of Promoters Are Found in Eukaryotic Nuclear Genes, One for Each Type of RNA Polymeras
- General Transcription Factors Are Involved in the Transcription of All Nuclear Genes
- Elongation, Termination, and RNA Cleavage Are Involved in Completing Eukaryotic RNA Synthesis
- 18.3 RNA Processing and Turnover
- The Nucleolus Is Involved in Ribosome Formation
- Ribosomal RNA Processing Involves Cleavage of Multiple rRNAs from a Common Precursor
- Transfer RNA Processing Involves Removal, Addition, and Chemical Modification of Nucleotides
- Messenger RNA Processing in Eukaryotes Involves Capping, Addition of Poly(A), and Removal of Introns
- Spliceosomes Remove Introns from Pre-mRNA
- Some Introns Are Self-Splicing
- The Existence of Introns Permits Alternative Splicing and Exon Shuffling
- Cells Localize Nuclear RNAs in Several Types of Processing Centers
- Nucleic Acid Editing Allows Sequences to Be Altered
- The C-Terminal Domain of RNA Polymerase II Coordinates RNA Processing
- Nuclear Export of Mature mRNA
- Most mRNA Molecules Have a Relatively Short Life Span
- The Abundance of mRNA Allows Amplification of Genetic Information
- Summary of Key Points
- Problem Set
- Key Technique: Hunting for DNA-Protein Interactions
- Human Connections: Death by Fungus (Amanita PhalloidesPoisoning)
- Chapter 19. Gene Expression: II. The Genetic Code and Protein Synthesis
- 19.1 The Genetic Code
- The Genetic Code Is a Triplet Code
- The Genetic Code Is Degenerate and Nonoverlapping
- Messenger RNA Guides the Synthesis of Polypeptide Chains
- The Codon Dictionary Was Established Using Synthetic RNA Polymers and Triplets
- Of the 64 Possible Codons in Messenger RNA, 61 Encode Amino Acids
- The Genetic Code Is (Nearly) Universal
- Codon Usage Bias
- 19.2 Translation: The Cast of Characters
- Ribosomes Carry Out Polypeptide Synthesis
- Transfer RNA Molecules Bring Amino Acids to the Ribosome
- Aminoacyl-tRNA Synthetases Link Amino Acids to the Correct Transfer RNAs
- Messenger RNA Brings Polypeptide Coding Information to the Ribosome
- Protein Factors Are Required for Translational Initiation, Elongation, and Termination
- 19.3 The Mechanism of Translation
- Translational Initiation Requires Initiation Factors, Ribosomal Subunits, mRNA, and Initiator tRNA
- Chain Elongation Involves Cycles of Aminoacyl tRNA Binding, Peptide Bond Formation, and Translocatio
- Most mRNAs Are Read by Many Ribosomes Simultaneously
- Termination of Polypeptide Synthesis Is Triggered by Release Factors That Recognize Stop Codons
- Polypeptide Folding Is Facilitated by Molecular Chaperones
- Protein Synthesis Typically Utilizes a Substantial Fraction of a Cell’s Energy Budget
- A Summary of Translation
- 19.4 Mutations and Translation
- Suppressor tRNAs Overcome the Effects of Some Mutations
- Nonsense-Mediated Decay and Nonstop Decay Promote the Destruction of Defective mRNAs
- 19.5 Posttranslational Processing
- Summary of Key Points
- Problem Set
- Human Connections: To Catch a Killer: The Problem of Antibiotic Resistance In Bacteria
- Key Technique: Protein Localization Using Fluorescent Fusion Proteins
- Chapter 20. The Regulation of Gene Expression
- 20.1 Bacterial Gene Regulation
- Catabolic and Anabolic Pathways Are Regulated Through Induction and Repression, Respectively
- The Genes Involved in Lactose Catabolism Are Organized into an Inducible Operon
- The lac Operon Is Negatively Regulated by the lac Repressor
- Studies of Mutant Bacteria Revealed How the lac Operon Is Organized
- Catabolite Activator Protein (CAP) Positively Regulates the lac Operon
- The lac Operon Is an Example of the Dual Control of Gene Expression
- The Structure of the lac Repressor/Operator Complex Confirms the Operon Model
- The Genes Involved in Tryptophan Synthesis Are Organized into a Repressible Operon
- Sigma Factors Determine Which Sets of Genes Can Be Expressed
- Attenuation Allows Transcription to Be Regulated After the Initiation Step
- Riboswitches Allow Transcription and Translation to Be Controlled by Small-Molecule Interactions wit
- The CRISPR/Cas System Protects Bacteria Against Viral Infection
- 20.2 Eukaryotic Gene Regulation: Genomic Control
- Multicellular Eukaryotes Are Composed of Numerous Specialized Cell Types
- Eukaryotic Gene Expression Is Regulated at Five Main Levels
- The Cells of a Multicellular Organism Usually Contain the Same Set of Genes
- Gene Amplification and Deletion Can Alter the Genome
- DNA Rearrangements Can Alter the Genome
- Chromatin Decondensation Is Involved in Genomic Control
- DNA Methylation Is Associated with Inactive Regions of the Genome
- 20.3 Eukaryotic Gene Regulation: Transcriptional Control
- Different Sets of Genes Are Transcribed in Different Cell Types
- Proximal Control Elements Lie Close to the Promoter
- Enhancers and Silencers Are DNA Elements Located at Variable Distances from the Promoter
- Coactivators Mediate the Interaction Between Regulatory Transcription Factors and the RNA Polymerase
- Multiple DNA Control Elements and Transcription Factors Act in Combination
- DNA-Binding and Activation Domains of Regulatory Transcription Factors Are Functionally Separable
- Several Common Types of Transcription Factors Bind to DNA and Activate Transcription
- DNA Response Elements Coordinate the Expression of Nonadjacent Genes
- Steroid Hormone Receptors Act as Transcription Factors That Bind to Hormone Response Elements
- CREBs and STATs Are Examples of Transcription Factors Activated by Phosphorylation
- The Heat Shock Response Element Coordinates Stress Responses
- Homeotic Genes Encode Transcription Factors That Regulate Embryonic Development
- 20.4 Eukaryotic Gene Regulation: Posttranscriptional Control
- Control of RNA Processing and Nuclear Export Follows Transcription
- Translation Rates Can Be Controlled by Initiation Factors and Translational Repressors
- Translation Can Also Be Controlled by Regulation of mRNA Degradation
- RNA Interference Utilizes Small RNAs to Silence Gene Expression
- MicroRNAs Produced by Normal Cellular Genes Silence the Translation of mRNAs
- Piwi-Interacting RNAs Are Small Regulatory RNAs That Protect the Germline of Eukaryotes
- Long Noncoding RNAs Play a Variety of Roles in Eukaryotic Gene Regulation
- Posttranslational Control Involves Modifications of Protein Structure, Function, and Degradation
- Ubiquitin Targets Proteins for Degradation by Proteasomes
- A Summary of Eukaryotic Gene Regulation
- Summary of Key Points
- Problem Set
- Human Connections: The Epigenome: Methylation and Disease
- Key Technique: Gene Knockdown via RNAi
- Chapter 21. Molecular Biology Techniques for Cell Biology
- 21.1 Analyzing, Manipulating, and Cloning DNA
- PCR Is Widely Used to Clone Genes
- Restriction Endonucleases Cleave DNA Molecules at Specific Sites
- Gel Electrophoresis Allows DNA to Be Separated by Size
- Restriction Mapping Can Characterize DNA
- Southern Blotting Identifies Specific DNAs from a Mixture
- Restriction Enzymes Allow Production of Recombinant DNA
- DNA Cloning Can Use Bacterial Cloning Vectors
- Genomic and cDNA Libraries Are Both Useful for DNA Cloning
- 21.2 Sequencing and Analyzing Genomes
- Rapid Procedures Exist for DNA Sequencing
- Whole Genomes Can Be Sequenced
- Comparative Genomics Allows Comparison of Genomes and Genes Within Them
- The Field of Bioinformatics Helps Decipher Genomes
- Tiny Differences in Genome Sequence Distinguish People from One Another
- 21.3 Analyzing RNA and Proteins
- Several Techniques Allow Detection of mRNAs in Time and Space
- The Transcription of Thousands of Genes Can Be Assessed Simultaneously
- Proteins Can Be Studied Using Electrophoresis
- Antibodies Can Be Used to Study Specific Proteins
- Proteins Can Be Isolated by Size, Charge, or Affinity
- Proteins Can Be Identified from Complex Mixtures Using Mass Spectrometry
- Protein Function Can Be Studied Using Molecular Biology Techniques
- Protein-Protein Interactions Can Be Studied in a Variety of Ways
- 21.4 Analyzing and Manipulating Gene Function
- Transgenic Organisms Carry Foreign Genes That Are Passed on to Subsequent Generations
- Transcriptional Reporters Are Useful for Studying Regulation of Gene Expression
- The Role of Specific Genes Can Be Assessed By Identifying Mutations and by Knockdown
- Genetic Engineering Can Produce Valuable Proteins That Are Otherwise Difficult to Obtain
- Food Crops Can Be Genetically Modified
- Gene Therapies Are Being Developed for the Treatment of Human Diseases
- Summary of Key Points
- Problem Set
- Key Technique: The Polymerase Chain Reaction (PCR)
- Human Connections: More Than Your Fingertips: Identifying Genetic “Fingerprints”
- Chapter 22. Signal Transduction Mechanisms: I. Electrical and Synaptic Signaling in Neurons
- 22.1 Neurons and Membrane Potential
- Neurons Are Specially Adapted to Transmit Electrical Signals
- Neurons Undergo Changes in Membrane Potential
- Neurons Display Electrical Excitability
- Resting Membrane Potential Depends on Ion Concentrations and Selective Membrane Permeability
- The Nernst Equation Describes the Relationship Between Membrane Potential and Ion Concentration
- Steady-State Ion Concentrations Affect Resting Membrane Potential
- The Goldman Equation Describes the Combined Effects of Ions on Membrane Potential
- 22.2 Electrical Excitability and the Action Potential
- Patch Clamping and Molecular Biological Techniques Allow Study of Single Ion Channels
- Specific Domains of Voltage-Gated Channels Act as Sensors and Inactivators
- Action Potentials Propagate Electrical Signals Along an Axon
- Action Potentials Involve Rapid Changes in the Membrane Potential of the Axon
- Action Potentials Result from the Rapid Movement of Ions Through Axonal Membrane Channels
- Action Potentials Are Propagated Along the Axon Without Losing Strength
- The Myelin Sheath Acts Like an Electrical Insulator Surrounding the Axon
- 22.3 Synaptic Transmission and Signal Integration
- Neurotransmitters Relay Signals Across Nerve Synapses
- Elevated Calcium Levels Stimulate Secretion of Neurotransmitters from Presynaptic Neurons
- Secretion of Neurotransmitters Involves the Docking and Fusion of Vesicles with the Plasma Membrane
- Neurotransmitters Are Detected by Specific Receptors on Postsynaptic Neurons
- Neurotransmitters Must Be Inactivated Shortly After Their Release
- Postsynaptic Potentials Integrate Signals from Multiple Neurons
- Summary of Key Points
- Problem Set
- Key Technique: Patch Clamping
- Human Connections: The Toxic Price of the Fountain of Youth
- Chapter 23. Signal Transduction Mechanisms: II. Messengers and Receptors
- 23.1 Chemical Signals and Cellular Receptors
- Chemical Signaling Involves Several Key Components
- Receptor Binding Involves Quantitative Interactions Between Ligands and Their Receptors
- Cells Can Amplify Signals Once They Are Received
- Cell-Cell Signals Act Through a Limited Number of Receptors and Signal Transduction Pathways
- 23.2 G Protein–Coupled Receptors
- G Protein–Coupled Receptors Act via Hydrolysis of GTP
- Cyclic AMP Is a Second Messenger Whose Production Is Regulated by Some G Proteins
- Disruption of G Protein Signaling Causes Human Disease
- Many G Proteins Act Through Inositol Trisphosphate and Diacylglycerol
- The Release of Calcium Ions Is a Key Event in Many Signaling Processes
- 23.3 Enzyme-Coupled Receptors
- Growth Factors Often Bind Protein Kinase-Associated Receptors
- Receptor Tyrosine Kinases Aggregate and Undergo Autophosphorylation
- Receptor Tyrosine Kinases Initiate a Signal Transduction Cascade Involving Ras and MAP Kinase
- The Key Steps in RTK Signaling Can Be Dissected Using Mutants
- Receptor Tyrosine Kinases Activate a Variety of Other Signaling Pathways
- Other Growth Factors Transduce Their Signals via Receptor Serine-Threonine Kinases
- Other Enzyme-Coupled Receptors Families
- 23.4 Putting It All Together: Signal Integration
- Scaffolding Complexes Can Facilitate Cell Signaling
- Different Signaling Pathways Are Integrated Through Crosstalk
- 23.5 Hormones and Other Long-Range Signals
- Hormones Can Be Classified by Their Chemical Properties
- The Endocrine System Controls Multiple Signaling Pathways to Regulate Glucose Levels
- Steroid Hormones Bind Hormones in the Cytosol and Carry Them into the Nucleus
- Gases Can Act as Cell Signals
- Summary of Key Points
- Problem Set
- Key Technique: Calcium Indicators and Ionophores
- Human Connections: The Gas That Prevents a Heart Attack
- Chapter 24. The Cell Cycle and Mitosis
- 24.1 Overview of the Cell Cycle
- 24.2 Nuclear and Cell Division
- Mitosis Is Subdivided into Prophase, Prometaphase, Metaphase, Anaphase, and Telophase
- The Mitotic Spindle Is Responsible for Chromosome Movements During Mitosis
- Cytokinesis Divides the Cytoplasm
- Bacteria and Eukaryotic Organelles Divide in a Different Manner from Eukaryotic Cells
- 24.3 Regulation of the Cell Cycle
- Cell Cycle Length Varies Among Different Cell Types
- Cell Cycle Progression Is Controlled at Several Key Transition Points
- Cell Fusion Experiments and Cell Cycle Mutants Identified Molecules That Control the Cell Cycle
- The Cell Cycle Is Controlled by Cyclin-Dependent Kinases (Cdks)
- Cdk-Cyclin Complexes Are Tightly Regulated
- The Anaphase-Promoting Complex Allows Exit from Mitosis
- Checkpoint Pathways Monitor Key Steps in the Cell Cycle
- 24.4 Growth Factors and Cell Proliferation
- Stimulatory Growth Factors Activate the Ras Pathway
- Stimulatory Growth Factors Can Also Activate the PI 3-Kinase–Akt Pathway
- Inhibitory Growth Factors Act Through Cdk Inhibitors
- Putting It All Together: The Cell Cycle Regulation Machine
- 24.5 Apoptosis
- Apoptosis Is Triggered by Death Signals or Withdrawal of Survival Factors
- Summary of Key Points
- Problem Set
- Key Technique: Measuring Cells Millions at a Time
- Human Connections: What do Ethnobotany and Cancer Have in Common?
- Chapter 25. Sexual Reproduction, Meiosis, and Genetic Recombination
- 25.1 Sexual Reproduction
- Sexual Reproduction Produces Genetic Variety
- Gametes Are Haploid Cells Specialized for Sexual Reproduction
- 25.2 Meiosis
- The Life Cycles of Sexual Organisms Have Diploid and Haploid Phases
- Meiosis Converts One Diploid Cell into Four Haploid Cells
- Meiosis I Produces Two Haploid Cells That Have Chromosomes Composed of Sister Chromatids
- Meiosis II Resembles a Mitotic Division
- Defects in Meiosis Lead to Nondisjunction
- Sperm and Egg Cells Are Generated by Meiosis Accompanied by Cell Differentiation
- Meiotic Maturation of Oocytes Is Tightly Regulated
- 25.3 Genetic Variability: Segregation and Assortment of Alleles
- Meiosis Generates Genetic Diversity
- Information Specifying Recessive Traits Can Be Present Without Being Displayed
- Alleles of Each Gene Segregate from Each Other During Gamete Formation
- Alleles of Each Gene Segregate Independently of the Alleles of Other Genes
- Chromosome Behavior Explains the Laws of Segregation and Independent Assortment
- The DNA Molecules of Homologous Chromosomes Have Similar Base Sequences
- 25.4 Genetic Variability: Recombination and Crossing Over
- Chromosomes Contain Groups of Linked Genes That Are Usually Inherited Together
- Homologous Chromosomes Exchange Segments During Crossing Over
- Gene Locations Can Be Mapped by Measuring Recombination Frequencies
- 25.5 Genetic Recombination in Bacteria and Viruses
- Co-infection of Bacterial Cells with Related Bacteriophages Can Lead to Genetic Recombination
- Recombination in Bacteria Can Occur via Transformation or Transduction
- Conjugation Is a Modified Sexual Activity That Facilitates Genetic Recombination in Bacteria
- 25.6 Mechanisms of Homologous Recombination
- DNA Breakage and Exchange Underlie Homologous Recombination Between Chromosomes
- The Synaptonemal Complex Facilitates Homologous Recombination During Meiosis
- Homologous Recombination Between Chromosomes Relies on High-Fidelity DNA Repair
- Summary of Key Points
- Problem Set
- Human Connections: When Meiosis Goes Awry
- Key Technique: Using Mendel’s Rules to Predict Human Disease
- Chapter 26. Cancer Cells
- 26.1 How Cancers Arise
- Tumors Arise When the Balance Between Cell Division and Cell Differentiation or Death Is Disrupted
- Cancer Cell Proliferation Is Anchorage Independent and Insensitive to Population Density
- Cancer Cells Are Immortalized by Mechanisms That Maintain Telomere Length
- Defects in Signaling Pathways, Cell Cycle Controls, and Apoptosis Contribute to Cancer
- Cancer Arises Through a Multistep Process Involving Initiation, Promotion, and Tumor Progression
- 26.2 How Cancers Spread
- Angiogenesis Is Required for Tumors to Grow Beyond a Few Millimeters in Diameter
- Blood Vessel Growth Is Controlled by a Balance Between Angiogenesis Activators and Inhibitors
- Cancer Cells Spread by Invasion and Metastasis
- Changes in Cell Adhesion, Motility, and Protease Production Promote Metastasis
- Relatively Few Cancer Cells Survive the Voyage Through the Bloodstream
- Blood Flow and Organ-Specific Factors Determine Sites of Metastasis
- The Immune System Influences the Growth and Spread of Cancer Cells
- The Tumor Microenvironment Influences Tumor Growth, Invasion, and Metastasis
- 26.3 What Causes Cancer?
- Epidemiological Data Have Allowed Many Causes of Cancer to Be Identified
- Errors in DNA Replication or Repair Explain Many Cancers
- Inborn Errors Explain Some Cancers
- Many Chemicals Can Cause Cancer, Often After Metabolic Activation in the Liver
- DNA Mutations Triggered by Chemical Carcinogens Lead to Cancer
- Ionizing and Ultraviolet Radiation Also Cause DNA Mutations That Lead to Cancer
- Viruses and Other Infectious Agents Trigger the Development of Some Cancers
- 26.4 Oncogenes and Tumor Suppressor Genes
- Oncogenes Are Genes Whose Products Can Trigger the Development of Cancer
- Proto-oncogenes Are Converted into Oncogenes by Several Distinct Mechanisms
- Most Oncogenes Encode Components of Growth-Signaling Pathways
- Tumor Suppressor Genes Are Genes Whose Loss or Inactivation Can Lead to Cancer
- The RB Tumor Suppressor Gene Was Discovered by Studying Families with Hereditary Retinoblastoma
- The p53 Tumor Suppressor Gene Is the Most Frequently Mutated Gene in Human Cancers
- The APC Tumor Suppressor Gene Encodes a Protein That Inhibits the Wnt Signaling Pathway
- Inactivation of Some Tumor Suppressor Genes Leads to Genetic Instability
- Cancers Develop by the Stepwise Accumulation of Mutations Involving Oncogenes and Tumor Suppressor G
- Epigenetic Changes in Gene Expression Influence the Properties of Cancer Cells
- Summing Up: Carcinogenesis and the Hallmarks of Cancer
- 26.5 Diagnosis, Screening, and Treatment
- Cancer Is Diagnosed by Microscopic and Molecular Examination of Tissue Specimens
- Screening Techniques for Early Detection Can Prevent Cancer Deaths
- Surgery, Radiation, and Chemotherapy Are Standard Treatments for Cancer
- Molecular Targeting Can Attack Cancer Cells More Specifically Than Chemotherapy
- Using the Immune System to Target Cancer Cells
- Cancer Treatments Can Be Tailored to Individual Patients
- Summary of Key Points
- Problem Set
- Human Connections: Molecular Sleuthing in Cancer Diagnosis
- Key Technique: Targeting Molecules in the Fight Against Cancer
- Appendix Visualizing Cells And Molecules
- Answer Key To Concept Check And Key Technique Questions
- Glossary
- Photo, Illustration, And Text Credits
- Index
- A
- B
- C
- D
- E
- F
- G
- H
- I
- J
- K
- L
- M
- N
- O
- P
- Q
- R
- S
- T
- U
- V
- W
- X
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