Becker’s World of the Cell, Global Edition

Höfundur Jeff Hardin; Gregory Paul Bertoni; Lewis J. Kleinsmith

Útgefandi Pearson International Content

Snið Page Fidelity

Print ISBN 9781292426525

Útgáfa 10

Höfundarréttur 2022

4.990 kr.

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
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