Concepts of Genetics, Global Edition
Námskeið
- LÆK310G Sameindalífvísindi A
- ERF1106 Erfðafræði.
Ensk lýsing:
For all introductory genetics courses. Teach students core genetics concepts and applications Concepts of Genetics emphasizes the fundamental ideas of genetics, while exploring modern techniques and applications of genetic analysis. This best-selling text continues to provide understandable explanations of complex, analytical topics and recognizes the importance of teaching students how to become effective problem solvers.
The 12th Edition has been extensively updated to provide comprehensive coverage of important, emerging topics such as CRISPR-Cas and the study of posttranscriptional gene regulation in eukaryotes. An expanded emphasis on ethical considerations that genetics is bringing into everyday life is addressed in Genetics, Ethics, and Society and Case Study features. Mastering Genetics is not included. Students, if Mastering Genetics is a recommended/mandatory component of the course, please ask your instructor for the correct ISBN.
Mastering Genetics should only be purchased when required by an instructor. Instructors, contact your Pearson representative for more information. Reach every student by pairing this text with Mastering Genetics Mastering™ is the teaching and learning platform that empowers you to reach every student. By combining trusted author content with digital tools and a flexible platform, Mastering personalizes the learning experience and improves results for each student.
Lýsing:
For all introductory genetics courses. Concepts of Genetics emphasises the fundamental ideas of genetics, while exploring modern techniques and applications of genetic analysis. This best-selling text continues to provide understandable explanations of complex, analytical topics and recognises the importance of teaching students how to become effective problem solvers. The 12th Edition has been extensively updated to provide comprehensive coverage of important, emerging topics such as CRISPR-Cas and the study of posttranscriptional gene regulation in eukaryotes.
An expanded emphasis on ethical considerations that genetics is bringing into everyday life is addressed in Genetics, Ethics, and Society and Case Study features. The full text downloaded to your computer With eBooks you can: search for key concepts, words and phrases make highlights and notes as you study share your notes with friends eBooks are downloaded to your computer and accessible either offline through the Bookshelf (available as a free download), available online and also via the iPad and Android apps.
Annað
- Höfundar: William S Klug, Michael Cummings, Charlotte A. Spencer, Michael A. Palladino, Darrell Killian
- Útgáfa:12
- Útgáfudagur: 2019-02-26
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- Format:Page Fidelity
- ISBN 13: 9781292265513
- Print ISBN: 9781292265322
- ISBN 10: 1292265515
Efnisyfirlit
- Title Page
- Copyright Page
- About the Authors
- Brief Contents
- Contents
- PART ONE GENES, CHROMOSOMES, AND HEREDITY
- 1 Introduction to Genetics
- 1.1 Genetics Has a Rich and Interesting History
- 1600–1850: The Dawn of Modern Biology
- Charles Darwin and Evolution
- 1.2 Genetics Progressed from Mendel to DNA in Less Than a Century
- Mendel’s Work on Transmission of Traits
- The Chromosome Theory of Inheritance: Uniting Mendel and Meiosis
- Genetic Variation
- The Search for the Chemical Nature of Genes: DNA or Protein?
- 1.3 Discovery of the Double Helix Launched the Era of Molecular Genetics
- The Structure of DNA and RNA
- Gene Expression: From DNA to Phenotype
- Proteins and Biological Function
- Linking Genotype to Phenotype: Sickle‐Cell Anemia
- 1.4 Development of Recombinant DNA Technology Began the Era of DNA Cloning
- 1.5 The Impact of Biotechnology Is Continually Expanding
- Plants, Animals, and the Food Supply
- Biotechnology in Genetics and Medicine
- 1.6 Genomics, Proteomics, and Bioinformatics Are New and Expanding Fields
- Modern Approaches to Understanding Gene Function
- 1.7 Genetic Studies Rely on the Use of Model Organisms
- The Modern Set of Genetic Model Organisms
- Model Organisms and Human Diseases
- 1.8 We Live in the Age of Genetics
- The Nobel Prize and Genetics
- Genetics, Ethics, and Society
- Summary Points
- Problems and Discussion Questions
- 1.1 Genetics Has a Rich and Interesting History
- 2 Mitosis and Meiosis
- 2.1 Cell Structure Is Closely Tied to Genetic Function
- 2.2 Chromosomes Exist in Homologous Pairs in Diploid Organisms
- 2.3 Mitosis Partitions Chromosomes into Dividing Cells
- Interphase and the Cell Cycle
- Prophase
- Prometaphase and Metaphase
- Anaphase
- Telophase
- Cell‐Cycle Regulation and Checkpoints
- 2.4 Meiosis Creates Haploid Gametes and Spores and Enhances Genetic Variation in Species
- Meiosis: Prophase I
- Metaphase, Anaphase, and Telophase I
- The Second Meiotic Division
- 2.5 The Development of Gametes Varies in Spermatogenesis Compared to Oogenesis
- 2.6 Meiosis Is Critical to Sexual Reproduction in All Diploid Organisms
- 2.7 Electron Microscopy Has Revealed the Physical Structure of Mitotic and Meiotic Chromosomes
- EXPLORING GENOMICS PubMed: Exploring and Retrieving Biomedical Literature
- CASE STUDY Timing is everything
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 3 Mendelian Genetics
- 3.1 Mendel Used a Model Experimental Approach to Study Patterns of Inheritance
- 3.2 The Monohybrid Cross Reveals How One Trait Is Transmitted from Generation to Generation
- Mendel’s First Three Postulates
- Modern Genetic Terminology
- Punnett Squares
- The Testcross: One Character
- 3.3 Mendel’s Dihybrid Cross Generated a Unique Ratio
- Mendel’s Fourth Postulate: Independent Assortment
- The Testcross: Two Characters
- MODERN APPROACHES TO UNDERSTANDING GENE FUNCTION Identifying Mendel’s Gene for Regulating White Fl
- 3.4 The Trihybrid Cross Demonstrates That Mendel’s Principles Apply to Inheritance of Multiple Tra
- The Forked‐Line Method, or Branch Diagram
- 3.5 Mendel’s Work Was Rediscovered in the Early Twentieth Century
- Unit Factors, Genes, and Homologous Chromosomes
- Evolving Concept of the Gene
- 3.6 Independent Assortment Leads to Extensive Genetic Variation
- 3.7 Laws of Probability Help to Explain Genetic Events
- 3.8 Chi‐Square Analysis Evaluates the Influence of Chance on Genetic Data
- Chi‐Square Calculations and the Null Hypothesis
- Interpreting Probability Values
- 3.9 Pedigrees Reveal Patterns of Inheritance of Human Traits
- Pedigree Conventions
- Pedigree Analysis
- 3.10 Mutant Phenotypes Have Been Examined at the Molecular Level
- How Mendel’s Peas Become Wrinkled: A Molecular Explanation
- Tay—Sachs Disease: The Molecular Basis of a Recessive Disorder in Humans
- EXPLORING GENOMICS Online Mendelian Inheritance in Man
- CASE STUDY To test or not to test
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 4 Extensions of Mendelian Genetics
- 4.1 Alleles Alter Phenotypes in Different Ways
- 4.2 Geneticists Use a Variety of Symbols for Alleles
- 4.3 Neither Allele Is Dominant in Incomplete, or Partial, Dominance
- 4.4 In Codominance, the Influence of Both Alleles in a Heterozygote Is Clearly Evident
- 4.5 Multiple Alleles of a Gene May Exist in a Population
- The ABO Blood Groups
- The A and B Antigens
- The Bombay Phenotype
- The white Locus in Drosophila
- 4.6 Lethal Alleles Represent Essential Genes
- The Molecular Basis of Dominance, Recessiveness, and Lethality: The agouti Gene
- 4.7 Combinations of Two Gene Pairs with Two Modes of Inheritance Modify the 9:3:3:1 Ratio
- Evolving Concept of the Gene
- 4.8 Phenotypes Are Often Affected by More Than One Gene
- Epistasis
- Novel Phenotypes
- Other Modified Dihybrid Ratios
- 4.9 Complementation Analysis Can Determine if Two Mutations Causing a Similar Phenotype Are Alleles
- 4.10 Expression of a Single Gene May Have Multiple Effects
- 4.11 X‐Linkage Describes Genes on the X Chromosome
- X‐Linkage in Drosophila
- X‐Linkage in Humans
- 4.12 In Sex‐Limited and Sex‐Influenced Inheritance, an Individual’s Sex Influences the Phenoty
- 4.13 Genetic Background and the Environment May Alter Phenotypic Expression
- Penetrance and Expressivity
- Genetic Background: Position Effects
- Temperature Effects—An Introduction to Conditional Mutations
- Nutritional Effects
- Onset of Genetic Expression
- Genetic Anticipation
- GENETICS, ETHICS, AND SOCIETY Nature versus Nurture: Is the Debate Over?
- CASE STUDY Should the child be deaf?
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 5 Sex Determination and Sex Chromosomes
- 5.1 X and Y Chromosomes Were First Linked to Sex Determination Early in the Twentieth Century
- 5.2 The Y Chromosome Determines Maleness in Humans
- Klinefelter and Turner Syndromes
- 47,XXX Syndrome
- 47,XYY Condition
- Sexual Differentiation in Humans
- The Y Chromosome and Male Development
- 5.3 The Ratio of Males to Females in Humans Is Not 1.0
- 5.4 Dosage Compensation Prevents Excessive Expression of X‐Linked Genes in Humans and Other Mammal
- Barr Bodies
- The Lyon Hypothesis
- The Mechanism of Inactivation
- 5.5 The Ratio of X Chromosomes to Sets of Autosomes Can Determine Sex
- D. melanogaster
- Caenorhabditis elegans
- MODERN APPROACHES TO UNDERSTANDING GENE FUNCTION Drosophila Sxl Gene Induces Female Development
- 5.6 Temperature Variation Controls Sex Determination in Many Reptiles
- GENETICS, ETHICS, AND SOCIETY A Question of Gender: Sex Selection in Humans
- CASE STUDY IS it a boy or a girl?
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 6 Chromosomal Mutations: Variation in Number and Arrangement
- 6.1 Variation in Chromosome Number: Terminology and Origin
- 6.2 Monosomy and Trisomy Result in a Variety of Phenotypic Effects
- Monosomy
- Trisomy
- Down Syndrome: Trisomy 21
- The Down Syndrome Critical Region (DSCR)
- MODERN APPROACHES TO UNDERSTANDING GENE FUNCTION Mouse Models of Down Syndrome
- The Origin of the Extra Chromosome 21 in Down Syndrome
- Human Aneuploidy
- 6.3 Polyploidy, in Which More Than Two Haploid Sets of Chromosomes Are Present, Is Prevalent in Plan
- Autopolyploidy
- Allopolyploidy
- Endopolyploidy
- 6.4 Variation Occurs in the Composition and Arrangement of Chromosomes
- 6.5 A Deletion Is a Missing Region of a Chromosome
- Cri du Chat Syndrome in Humans
- 6.6 A Duplication Is a Repeated Segment of a Chromosome
- Gene Redundancy and Amplification—Ribosomal RNA Genes
- The Bar Mutation in Drosophila
- The Role of Gene Duplication in Evolution
- Duplications at the Molecular Level: Copy Number Variations (CNVs)
- 6.7 Inversions Rearrange the Linear Gene Sequence
- Consequences of Inversions during Gamete Formation
- Evolutionary Advantages of Inversions
- 6.8 Translocations Alter the Location of Chromosomal Segments in the Genome
- Translocations in Humans: Familial Down Syndrome
- 6.9 Fragile Sites in Human Chromosomes Are Susceptible to Breakage
- Fragile‐X Syndrome
- The Link between Fragile Sites and Cancer
- GENETICS, ETHICS, AND SOCIETY Down Syndrome and Prenatal Testing—The New Eugenics?
- CASE STUDY Fish tales
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 7 Chromosome Mapping in Eukaryotes
- 7.1 Genes Linked on the Same Chromosome Segregate Together
- The Linkage Ratio
- 7.2 Crossing Over Serves as the Basis for Determining the Distance between Genes in Chromosome Mappi
- Morgan and Crossing Over
- Sturtevant and Mapping
- Single Crossovers
- 7.3 Determining the Gene Sequence during Mapping Requires the Analysis of Multiple Crossovers
- Multiple Exchanges
- Three‐Point Mapping in Drosophila
- Determining the Gene Sequence
- An Autosomal Mapping Problem in Maize
- 7.4 As the Distance between Two Genes Increases, Mapping Estimates Become More Inaccurate
- Interference and the Coefficient of Coincidence
- 7.5 Drosophila Genes Have Been Extensively Mapped
- Evolving Concept of the Gene
- 7.6 Lod Score Analysis and Somatic Cell Hybridization Were Historically Important in Creating Human
- 7.7 Chromosome Mapping Is Currently Performed Using DNA Markers and Annotated Computer Databases
- 7.8 Crossing Over Involves a Physical Exchange between Chromatids
- 7.9 Exchanges Also Occur between Sister Chromatids during Mitosis
- EXPLORING GENOMICS Human Chromosome Maps on the Internet
- CASE STUDY Links to autism
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 7.1 Genes Linked on the Same Chromosome Segregate Together
- 8 Genetic Analysis and Mapping in Bacteria and Bacteriophages
- 8.1 Bacteria Mutate Spontaneously and Grow at an Exponential Rate
- 8.2 Genetic Recombination Occurs in Bacteria
- Conjugation in Bacteria: The Discovery of F+ and F– Strains
- Hfr Bacteria and Chromosome Mapping
- Recombination in F+ × F– Matings: A Reexamination
- The F State and Merozygotes
- 8.3 The F Factor Is an Example of a Plasmid
- 8.4 Transformation Is a Second Process Leading to Genetic Recombination in Bacteria
- The Transformation Process
- Transformation and Linked Genes
- 8.5 Bacteriophages Are Bacterial Viruses
- Phage T4: Structure and Life Cycle
- The Plaque Assay
- Lysogeny
- 8.6 Transduction Is Virus‐Mediated Bacterial DNA Transfer
- The Lederberg–Zinder Experiment
- Transduction and Mapping
- 8.7 Bacteriophages Undergo Intergenic Recombination
- Bacteriophage Mutations
- Mapping in Bacteriophages
- 8.8 Intragenic Recombination Occurs in Phage T4
- The rII Locus of Phage T4
- Complementation by rII Mutations
- Recombinational Analysis
- Deletion Testing of the rII Locus
- The rII Gene Map
- Evolving Concept of the Gene
- GENETICS, ETHICS, AND SOCIETY Multidrug‐Resistant Bacteria: Fighting with Phage
- CASE STUDY To treat or not to treat
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 9 Extranuclear Inheritance
- 9.1 Organelle Heredity Involves DNA in ‐Chloroplasts and Mitochondria
- Chloroplasts: Variegation in Four O’Clock Plants
- Chloroplast Mutations in Chlamydomonas
- Mitochondrial Mutations: Early Studies in Neurospora and Yeast
- 9.2 Knowledge of Mitochondrial and Chloroplast DNA Helps Explain Organelle Heredity
- Organelle DNA and the Endosymbiotic Theory
- Molecular Organization and Gene Products of ‐Chloroplast DNA
- Molecular Organization and Gene Products of ‐Mitochondrial DNA
- 9.3 Mutations in Mitochondrial DNA Cause Human Disorders
- Mitochondria, Human Health, and Aging
- Future Prevention of the Transmission of mtDNA‐Based Disorders
- 9.4 In Maternal Effect, the Maternal Genotype Has a Strong Influence during Early Development
- Lymnaea Coiling
- Embryonic Development in Drosophila
- GENETICS, ETHICS, AND SOCIETY Mitochondrial Replacement and Three‐Parent Babies
- CASE STUDY Is it all in the genes?
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 9.1 Organelle Heredity Involves DNA in ‐Chloroplasts and Mitochondria
- 1 Introduction to Genetics
- 10 DNA Structure and Analysis
- 10.1 The Genetic Material Must Exhibit Four Characteristics
- 10.2 Until 1944, Observations Favored Protein as the Genetic Material
- 10.3 Evidence Favoring DNA as the Genetic Material Was First Obtained during the Study of Bacteria a
- Transformation: Early Studies
- Transformation: The Avery, MacLeod, and McCarty Experiment
- The Hershey–Chase Experiment
- Transfection Experiments
- 10.4 Indirect and Direct Evidence Supports the Concept That DNA Is the Genetic Material in Eukaryote
- Indirect Evidence: Distribution of DNA
- Indirect Evidence: Mutagenesis
- Direct Evidence: Recombinant DNA Studies
- 10.5 RNA Serves as the Genetic Material in Some Viruses
- 10.6 Knowledge of Nucleic Acid Chemistry Is Essential to the Understanding of DNA Structure
- Nucleotides: Building Blocks of Nucleic Acids
- Nucleoside Diphosphates and Triphosphates
- Polynucleotides
- 10.7 The Structure of DNA Holds the Key to Understanding Its Function
- Base‐Composition Studies
- X‐Ray Diffraction Analysis
- The Watson–Crick Model
- Evolving Concept of the Gene
- 10.8 Alternative Forms of DNA Exist
- 10.9 The Structure of RNA Is Chemically Similar to DNA, but Single Stranded
- 10.10 Many Analytical Techniques Have Been Useful during the Investigation of DNA and RNA
- Electrophoresis
- EXPLORING GENOMICS Introduction to Bioinformatics: BLAST
- CASE STUDY Credit where credit is due
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 11 DNA Replication and Recombination
- 11.1 DNA Is Reproduced by Semiconservative Replication
- The Meselson–Stahl Experiment
- Semiconservative Replication in Eukaryotes
- Origins, Forks, and Units of Replication
- 11.2 DNA Synthesis in Bacteria Involves Five ‐Polymerases, as Well as Other Enzymes
- DNA Polymerase I
- DNA Polymerase II, III, IV, and V
- The DNA Pol III Holoenzyme
- 11.3 Many Complex Issues Must Be Resolved during DNA Replication
- Unwinding the DNA Helix
- Initiation of DNA Synthesis Using an RNA Primer
- Continuous and Discontinuous DNA Synthesis
- Concurrent Synthesis Occurs on the Leading and Lagging Strands
- Proofreading and Error Correction Occurs during DNA Replication
- 11.4 A Coherent Model Summarizes DNA Replication
- 11.5 Replication Is Controlled by a Variety of Genes
- MODERN APPROACHES TO UNDERSTANDING GENE FUNCTION Lethal Knockouts
- 11.6 Eukaryotic DNA Replication Is Similar to Replication in Bacteria, but Is More Complex
- Initiation at Multiple Replication Origins
- Multiple Eukaryotic DNA Polymerases
- Replication through Chromatin
- 11.7 Telomeres Solve Stability and Replication Problems at Eukaryotic Chromosome Ends
- Telomere Structure and Chromosome Stability
- Telomeres and Chromosome End Replication
- Telomeres in Disease, Aging, and Cancer
- 11.8 Recombination Is Essential for Genetic Exchange and DNA Repair
- Models of Homologous Recombination
- GENETICS, ETHICS, AND SOCIETY Telomeres: The Key to a Long Life?
- CASE STUDY At loose ends
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 11.1 DNA Is Reproduced by Semiconservative Replication
- 12 DNA Organization in Chromosomes
- 12.1 Viral and Bacterial Chromosomes are Relatively Simple DNA Molecules
- 12.2 Supercoiling Facilitates Compaction of the DNA of Viral and Bacterial Chromosomes
- 12.3 Specialized Chromosomes Reveal Variations in the Organization of DNA
- Polytene Chromosomes
- Lampbrush Chromosomes
- 12.4 DNA Is Organized into Chromatin in Eukaryotes
- Chromatin Structure and Nucleosomes
- Chromatin Remodeling
- Heterochromatin
- 12.5 Chromosome Banding Differentiates Regions along the Mitotic Chromosome
- 12.6 Eukaryotic Genomes Demonstrate Complex Sequence Organization Characterized by Repetitive DNA
- Satellite DNA
- Centromeric DNA Sequences
- Middle Repetitive Sequences: VNTRs and STRs
- Repetitive Transposed Sequences: SINEs and LINEs
- Middle Repetitive Multiple‐Copy Genes
- 12.7 The Vast Majority of a Eukaryotic Genome Does Not Encode Functional Genes
- EXPLORING GENOMICS Database of Genomic Variants: Structural Variations in the Human Genome
- CASE STUDY Helping or hurting?
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 13 The Genetic Code and Transcription
- 13.1 The Genetic Code Uses Ribonucleotide Bases as “Letters”
- 13.2 Early Studies Established the Basic Operational Patterns of the Code
- The Triplet Nature of the Code
- 13.3 Studies by Nirenberg, Matthaei, and Others Led to Deciphering of the Code
- Synthesizing Polypeptides in a Cell‐Free System
- Homopolymer Codes
- The Use of Mixed Heteropolymers
- The Triplet Binding Assay
- Repeating Copolymers
- 13.4 The Coding Dictionary Reveals Several Interesting Patterns among the 64 Codons
- Degeneracy and the Wobble Hypothesis
- The Ordered Nature of the Code
- Punctuating the Code: Initiation and Termination Codons
- 13.5 The Genetic Code Has Been Confirmed in Studies of Phage MS2
- 13.6 The Genetic Code Is Nearly Universal
- 13.7 Different Initiation Points Create Overlapping Genes
- 13.8 Transcription Synthesizes RNA on a DNA Template
- 13.9 RNA Polymerase Directs RNA Synthesis
- Promoters, Template Binding, and the Subunit
- Initiation, Elongation, and Termination of RNA Synthesis in Bacteria
- 13.10 Transcription in Eukaryotes Differs from Bacterial Transcription in Several Ways
- Initiation of Transcription in Eukaryotes
- Recent Discoveries Concerning Eukaryotic RNA Polymerase Function
- Processing Eukaryotic RNA: Caps and Tails
- 13.11 The Coding Regions of Eukaryotic Genes Are Interrupted by Intervening Sequences Called Introns
- Why Do Introns Exist?
- Splicing Mechanisms: Self‐Splicing RNAs
- Splicing Mechanisms: The Spliceosome
- Evolving Concept of the Gene
- 13.12 RNA Editing May Modify the Final Transcript
- 13.13 Transcription Has Been Visualized by Electron Microscopy
- CASE STUDY Treatment dilemmas
- Summary Points
- GENETICS, ETHICS, AND SOCIETY Treating Duchenne Muscular Dystrophy with Exon‐Skipping Drugs
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 14 Translation and Proteins
- 14.1 Translation of mRNA Depends on Ribosomes and Transfer RNAs
- Ribosomal Structure
- tRNA Structure
- Charging tRNA
- 14.2 Translation of mRNA Can Be Divided into Three Steps
- Initiation
- Elongation
- Termination
- Polyribosomes
- 14.3 High‐Resolution Studies Have Revealed Many Details about the Functional Bacterial Ribosome
- 14.4 Translation Is More Complex in Eukaryotes
- 14.5 The Initial Insight That Proteins Are Important in Heredity Was Provided by the Study of Inborn
- Phenylketonuria
- 14.6 Studies of Neurospora Led to the One‐Gene:One‐Enzyme Hypothesis
- Analysis of Neurospora Mutants by Beadle and Tatum
- Genes and Enzymes: Analysis of Biochemical Pathways
- 14.7 Studies of Human Hemoglobin Established That One Gene Encodes One Polypeptide
- Sickle‐Cell Anemia
- Evolving Concept of the Gene
- 14.8 Variation in Protein Structure Provides the Basis of Biological Diversity
- 14.9 Posttranslational Modification Alters the Final Protein Product
- Protein Folding and Misfolding
- 14.10 Proteins Perform Many Diverse Roles
- 14.11 Proteins Often Include More Than One ‐Functional Domain
- Exon Shuffling
- Exploring Genomics Translation Tools and Swiss‐Prot for Studying ‐Protein Sequences
- CASE STUDY Crippled ribosomes
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 14.1 Translation of mRNA Depends on Ribosomes and Transfer RNAs
- 15 Gene Mutation, DNA Repair, and Transposition
- 15.1 Gene Mutations Are Classified in Various Ways
- Classification Based on Type of Molecular Change
- Classification Based on Effect on Function
- Classification Based on Location of Mutation
- 15.2 Mutations Occur Spontaneously and Randomly
- Spontaneous and Induced Mutations
- Spontaneous Germ‐Line Mutation Rates in Humans
- Spontaneous Somatic Mutation Rates in Humans
- The Fluctuation Test: Are Mutations Random or Adaptive?
- 15.3 Spontaneous Mutations Arise from ‐Replication Errors and Base Modifications
- DNA Replication Errors and Slippage
- Tautomeric Shifts
- Depurination and Deamination
- Oxidative Damage
- Transposable Elements
- 15.4 Induced Mutations Arise from DNA Damage Caused by Chemicals and Radiation
- Base Analogs
- Alkylating, Intercalating, and Adduct‐Forming Agents
- Ultraviolet Light
- Ionizing Radiation
- 15.5 Single‐Gene Mutations Cause a Wide Range of Human Diseases
- Single‐Gene Mutations and β‐Thalassemia
- Mutations Caused by Expandable DNA Repeats
- 15.6 Organisms Use DNA Repair Systems to Counteract Mutations
- Proofreading and Mismatch Repair
- Postreplication Repair and the SOS Repair System
- Photoreactivation Repair: Reversal of UV Damage
- Base and Nucleotide Excision Repair
- Nucleotide Excision Repair and Xeroderma ‐Pigmentosum in Humans
- Double‐Strand Break Repair in Eukaryotes
- 15.7 The Ames Test Is Used to Assess the Mutagenicity of Compounds
- 15.8 Transposable Elements Move within the Genome and May Create Mutations
- DNA Transposons
- DNA Transposons—the Ac–Ds System in Maize
- Retrotransposons
- Retrotransposons—the Copia –White‐Apricot ‐System in Drosophila
- Transposable Elements in Humans
- Transposable Elements, Mutations, and Evolution
- MODERN APPROACHES TO UNDERSTANDING GENE FUNCTION Transposon‐Mediated Mutations Reveal Genes Involv
- EXPLORING GENOMICS Sequence Alignment to Identify a Mutation
- CASE STUDY An Unexpected Diagnosis
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 15.1 Gene Mutations Are Classified in Various Ways
- 16 Regulation of Gene Expression in Bacteria
- 16.1 Bacteria Regulate Gene Expression in Response to Environmental Conditions
- 16.2 Lactose Metabolism in E. coli Is Regulated by an Inducible System
- Structural Genes
- The Discovery of Regulatory Mutations
- The Operon Model: Negative Control
- Genetic Proof of the Operon Model
- Isolation of the Repressor
- 16.3 The Catabolite‐Activating Protein (CAP) Exerts Positive Control over the lac Operon
- 16.4 Crystal Structure Analysis of Repressor ‐Complexes Has Confirmed the Operon Model
- 16.5 The Tryptophan (trp) Operon in E. coli Is a Repressible Gene System
- Evidence for the trp Operon
- Evolving Concept of the Gene
- 16.6 RNA Plays Diverse Roles in Regulating Gene Expression in Bacteria
- Attenuation
- Riboswitches
- Small Noncoding RNAs Play Regulatory Roles in Bacteria
- CASE STUDY MRSA in the National Football League (NFL)
- Summary Points
- GENETICS, ETHICS, AND SOCIETY Quorum Sensing: Social Networking and Gene Regulation in Bacteria
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 17 Transcriptional Regulation in Eukaryotes
- 17.1 Organization of the Eukaryotic Cell Facilitates Gene Regulation at Several Levels
- 17.2 Eukaryotic Gene Expression Is Influenced by Chromatin Modifications
- Chromosome Territories and Transcription Factories
- Open and Closed Chromatin
- Histone Modifications and Chromatin Remodeling
- DNA Methylation
- 17.3 Eukaryotic Transcription Initiation Requires Specific Cis‐Acting Sites
- Promoters and Promoter Elements
- Enhancers, Insulators, and Silencers
- 17.4 Eukaryotic Transcription Initiation Is Regulated by Transcription Factors That Bind to Cis‐Ac
- The Human Metallothionein 2A Gene: Multiple Cis‐Acting Elements and Transcription Factors
- Functional Domains of Eukaryotic Transcription Factors
- 17.5 Activators and Repressors Interact with General Transcription Factors and Affect Chromatin Stru
- Formation of the RNA Polymerase II Transcription Initiation Complex
- Mechanisms of Transcription Activation and Repression
- 17.6 Gene Regulation in a Model Organism: Transcription of the GAL Genes of Yeast
- 17.7 ENCODE Data Are Transforming Our Concepts of Eukaryotic Gene Regulation
- Enhancer and Promoter Elements
- Transcripts and Noncoding RNA
- Many Disease‐Associated Genome Variations Affect Regulatory Regions
- Evolving Concept of a Gene
- Exploring Genomics Tissue‐Specific Gene Expression
- CASE STUDY Risk assessment
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 18 Posttranscriptional Regulation in Eukaryotes
- 18.1 Regulation of Alternative Splicing Determines Which RNA Spliceforms of a Gene Are Translated
- Types of Alternative Splicing
- Alternative Splicing and the Proteome
- Regulation of Alternative Splicing
- Sex Determination in Drosophila: A Model for Regulation of Alternative Splicing
- Alternative Splicing and Human Diseases
- 18.2 Gene Expression Is Regulated by mRNA Stability and Degradation
- Mechanisms of mRNA Decay
- Regulation of mRNA Stability and Degradation
- mRNA Surveillance and Nonsense‐Mediated Decay
- 18.3 Noncoding RNAs Play Diverse Roles in ‐Posttranscriptional Regulation
- The Discovery of RNA Interference and microRNAs
- Mechanisms of RNA Interference
- RNA Interference in Research, Biotechnology, and Medicine
- Long Noncoding RNAs and Posttranscriptional Regulation
- Circular RNAs
- MODERN APPROACHES TO UNDERSTANDING GENE FUNCTION MicroRNAs Regulate Ovulation in Female Mice
- 18.4 mRNA Localization and Translation Initiation Are Highly Regulated
- Cytoplasmic Polyadenylation
- mRNA Localization and Localized Translational Control
- 18.5 Posttranslational Modifications Regulate ‐Protein Activity
- Regulation of Proteins by Phosphorylation
- Ubiquitin‐Mediated Protein Degradation
- GENETICS, ETHICS, AND SOCIETY Is DNA Enough?
- CASE STUDY A mysterious muscular dystrophy
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 18.1 Regulation of Alternative Splicing Determines Which RNA Spliceforms of a Gene Are Translated
- 19 Epigenetic Regulation of Gene Expression
- 19.1 Molecular Alterations to the Genome Create an Epigenome
- DNA Methylation and the Methylome
- Histone Modification and Chromatin Remodeling
- Short and Long Noncoding RNAs
- 19.2 Epigenetics and Monoallelic Gene Expression
- Parent‐of‐Origin Monoallelic Expression: Imprinting
- Random Monoallelic Expression: Inactivation of the X Chromosome
- Random Monoallelic Expression of Autosomal Genes
- Assisted Reproductive Technologies (ART) and Imprinting Defects
- 19.3 Epigenetics and Cancer
- DNA Methylation and Cancer
- Chromatin Remodeling and Histone Modification in Cancer
- Epigenetic Cancer Therapy
- 19.4 Epigenetic Traits Are Heritable
- Environmental Induction of Epigenetic Change
- Stress‐Induced Behavior Is Heritable
- 19.5 Epigenome Projects and Databases
- CASE STUDY Food for Thought
- Summary Points
- EXPLORING GENOMICS The International Human Epigenome Consortium (IHEC)
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 19.1 Molecular Alterations to the Genome Create an Epigenome
- 20 Recombinant DNA Technology
- 20.1 Recombinant DNA Technology Began with Two Key Tools: Restriction Enzymes and ‐Cloning Vectors
- Restriction Enzymes Cut DNA at Specific ‐Recognition Sequences
- DNA Vectors Accept and Replicate DNA Molecules to Be Cloned
- Bacterial Plasmid Vectors
- Other Types of Cloning Vectors
- Host Cells for Cloning Vectors
- 20.2 DNA Libraries Are Collections of Cloned Sequences
- Genomic Libraries
- Complementary DNA (cDNA) Libraries
- Specific Genes Can Be Recovered from a Library by Screening
- 20.3 The Polymerase Chain Reaction Is a Powerful Technique for Copying DNA
- PCR Limitations
- PCR Applications
- 20.4 Molecular Techniques for Analyzing DNA and RNA
- Restriction Mapping
- Nucleic Acid Blotting
- In Situ Hybridization
- 20.5 DNA Sequencing Is the Ultimate Way to Characterize DNA at the Molecular Level
- Sequencing Technologies Have Progressed Rapidly
- Next‐Generation Sequencing Technology
- Third‐Generation Sequencing Technology
- DNA Sequencing and Genomics
- 20.6 Creating Knockout and Transgenic Organisms for Studying Gene Function
- Gene Targeting and Knockout Animal Models
- Making a Transgenic Animal: The Basics
- Gene Editing with CRISPR‐Cas
- EXPLORING GENOMICS Manipulating Recombinant DNA: Restriction ‐Mapping and Designing PCR Primers
- CASE STUDY Ethical issues and genetic technology
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 20.1 Recombinant DNA Technology Began with Two Key Tools: Restriction Enzymes and ‐Cloning Vectors
- 21 Genomic Analysis
- 21.1 Genomic Analysis Before Modern Sequencing Methods Involved Classical Genetics Approaches and Cl
- 21.2 Whole‐Genome Sequencing Is Widely Used for Sequencing and Assembling Entire Genomes
- High‐Throughput Sequencing and Its Impact on Genomics
- The Clone‐by‐Clone Approach
- Draft Sequences and Reference Genomes
- 21.3 DNA Sequence Analysis Relies on Bioinformatics Applications and Genome Databases
- Annotation to Identify Gene Sequences
- Hallmark Characteristics of a Gene Sequence Can Be Recognized during Annotation
- 21.4 Functional Genomics Establishes Gene Function and Identifies Regulatory Elements in a Genome
- Predicting Gene and Protein Functions by Sequence Analysis
- Predicting Function from Structural Analysis of Protein Domains and Motifs
- Investigators Are Using Genomics Techniques Such as Chromatin Immunoprecipitation to Investigate Asp
- 21.5 The Human Genome Project Revealed Many Important Aspects of Genome Organization in Humans
- Origins of the Project
- Major Features of the Human Genome
- Individual Variations in the Human Genome
- Accessing the Human Genome Project on the Internet
- 21.6 The “Omics” Revolution Has Created a New Era of Biological Research
- After the HGP, What’s Next?
- Personal Genome Projects
- Somatic Genome Mosaicism and the Emerging Pangenome
- Whole‐Exome Sequencing
- Encyclopedia of DNA Elements (ENCODE) Project
- Nutrigenomics Considers Genetics and Diet
- No Genome Left Behind and the Genome 10K Plan
- Stone‐Age Genomics
- 21.7 Comparative Genomics Analyzes and Compares Genomes from Different Organisms
- Bacterial and Eukaryotic Genomes Display Common Structural and Functional Features and Important Dif
- Comparative Genomics Provides Novel Information about the Genomes of Model Organisms and the Human G
- The Sea Urchin Genome
- The Dog Genome
- The Chimpanzee Genome
- The Rhesus Monkey Genome
- The Neanderthal Genome and Modern Humans
- 21.8 Metagenomics Applies Genomics Techniques to Environmental Samples
- The Human Microbiome Project
- 21.9 Transcriptome Analysis Reveals Profiles of Expressed Genes in Cells and Tissues
- DNA Microarray Analysis
- RNA Sequencing Technology Allows for In Situ Analysis of Gene Expression
- 21.10 Proteomics Identifies and Analyzes the Protein Composition of Cells
- Reconciling the Number of Genes and the Number of Proteins Expressed by a Cell or Tissue
- Mass Spectrometry for Protein Identification
- EXPLORING GENOMICS Contigs, Shotgun Sequencing, and Comparative Genomics
- CASE STUDY Your microbiome may be a risk factor for disease
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 22 Applications of Genetic Engineering and Biotechnology
- 22.1 Genetically Engineered Organisms Synthesize a Variety of Valuable Biopharmaceutical Products
- Recombinant Protein Production in Bacteria
- Transgenic Animal Hosts and Biopharmaceutical Products
- Recombinant DNA Approaches for Vaccine Production
- Vaccine Proteins Can Be Produced by Plants
- DNA‐Based Vaccines
- 22.2 Genetic Engineering of Plants Has Revolutionized Agriculture
- 22.3 Genetically Modified Animals Serve Important Roles in Biotechnology
- Examples of Transgenic Animals
- 22.4 Genetic Testing, Including Genomic Analysis, Is Transforming Medical Diagnosis
- Genetic Testing for Prognostic or Diagnostic Purposes
- Prenatal Genetic Testing
- Genetic Testing Using Allele‐Specific Oligonucleotides
- Genetic Testing Using Microarrays
- Applications of Gene‐Expression Microarrays and Next–Generation Sequencing for Pathogen Identifi
- Screening the Genome for Genes or Mutations You Want
- 22.5 Genetic Analysis of Individual Genomes
- 22.6 Genetic Analysis from Single Cells
- 22.7 Genome‐Wide Association Studies Identify Genome Variations That Contribute to Disease
- 22.8 Synthetic Genomes and the Emergence of Synthetic Biology
- The Minimal Genome: How Many Essential Genes Are Required by a Living Cell?
- Design and Transplantation of a Synthetic Genome Defines the Minimal Bacterial Genome
- The Essential Genes of Human Cells and the Quest to Create a Synthetic Human Genome
- Synthetic Biology for Bioengineering Applications
- 22.9 Genetic Engineering, Genomics, and Biotechnology Raise Ethical, Social, and Legal Questions
- Genetic Testing and Ethical Dilemmas
- Direct‐to‐Consumer Genetic Testing and Regulating the Genetic Test Providers
- DNA and Gene Patents
- Whole‐Genome Sequence Analysis Presents Many Questions of Ethics
- Privacy and Anonymity in the Era of Genomic Big Data
- GENETICS, ETHICS, AND SOCIETY Privacy and Anonymity in the Era of Genomic Big Data
- Preconception Testing, Destiny Predictions, and Baby‐Predicting Patents
- Patents and Synthetic Biology
- CASE STUDY “Driving” to Extinction
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 22.1 Genetically Engineered Organisms Synthesize a Variety of Valuable Biopharmaceutical Products
- 23 Developmental Genetics
- 23.1 Differentiated States Develop from Coordinated Programs of Gene Expression
- Genetic and Epigenetic Regulation of Development
- 23.2 Evolutionary Conservation of Developmental Mechanisms Can Be Studied Using Model Organisms
- Analysis of Developmental Mechanisms
- 23.3 Genetic Analysis of Embryonic Development in Drosophila Reveals How the Body Axis of Animals Is
- Overview of Drosophila Development
- Genetic Analysis of Embryogenesis
- 23.4 Segment Formation and Body Plans in Drosophila and Mammals
- Gap Genes
- Pair‐Rule Genes
- Segment Polarity Genes
- Segmentation Genes in Mice and Humans
- 23.5 Homeotic Selector Genes Specify Body Parts of the Adult
- Hox Genes in Drosophila
- Hox Genes and Human Genetic Disorders
- 23.6 Plants Have Evolved Developmental Regulatory Systems That Parallel Those of Animals
- Homeotic Genes in Arabidopsis
- Divergence in Homeotic Genes
- 23.7 C. elegans Serves as a Model for Cell–Cell Interactions in Development
- Signaling Pathways in Development
- The Notch Signaling Pathway
- Overview of C. elegans Development
- Genetic Analysis of Vulva Formation
- MODERN APPROACHES TO UNDERSTANDING GENE FUNCTION Downregulating a Single Gene Reveals Secrets to Hea
- 23.8 Binary Switch Genes and Regulatory Networks Program Genomic Expression
- The Control of Eye Formation
- GENETICS, ETHICS, AND SOCIETY Stem Cell Wars
- CASE STUDY One foot or another
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 23.1 Differentiated States Develop from Coordinated Programs of Gene Expression
- 24 Cancer Genetics
- 24.1 Cancer Is a Genetic Disease at the Level of Somatic Cells
- What Is Cancer?
- The Clonal Origin of Cancer Cells
- Driver Mutations and Passenger Mutations
- The Cancer Stem Cell Hypothesis
- Cancer as a Multistep Process, Requiring Multiple Mutations and Clonal Expansions
- 24.2 Cancer Cells Contain Genetic Defects Affecting Genomic Stability, DNA Repair, and Chromatin Mod
- Genomic Instability and Defective DNA Repair
- Chromatin Modifications and Cancer Epigenetics
- 24.3 Cancer Cells Contain Genetic Defects Affecting Cell‐Cycle Regulation
- The Cell Cycle and Signal Transduction
- Cell‐Cycle Control and Checkpoints
- Control of Apoptosis
- Cancer Therapies and Cancer Cell Biology
- 24.4 Proto‐oncogenes and Tumor‐Suppressor Genes Are Altered in Cancer Cells
- The ras Proto‐oncogenes
- The TP53 Tumor‐Suppressor Gene
- 24.5 Cancer Cells Metastasize and Invade Other Tissues
- 24.6 Predisposition to Some Cancers Can Be Inherited
- 24.7 Viruses Contribute to Cancer in Both Humans and Animals
- 24.8 Environmental Agents Contribute to Human Cancers
- Natural Environmental Agents
- Human‐Made Chemicals and Pollutants
- Tobacco Smoke and Cancer
- CASE STUDY Cancer‐killing bacteria
- Summary Points
- Exploring Genomics The Cancer Genome Anatomy Project (CGAP)
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 24.1 Cancer Is a Genetic Disease at the Level of Somatic Cells
- 25 Quantitative Genetics and Multifactorial Traits
- 25.1 Not All Polygenic Traits Show Continuous Variation
- 25.2 Quantitative Traits Can Be Explained in ‐Mendelian Terms
- The Multiple‐Gene Hypothesis for Quantitative Inheritance
- Additive Alleles: The Basis of Continuous Variation
- Calculating the Number of Polygenes
- 25.3 The Study of Polygenic Traits Relies on Statistical Analysis
- The Mean
- Variance
- Standard Deviation
- Standard Error of the Mean
- Covariance and Correlation Coefficient
- Analysis of a Quantitative Character
- 25.4 Heritability Values Estimate the Genetic Contribution to Phenotypic Variability
- Broad‐Sense Heritability
- Narrow‐Sense Heritability
- Artificial Selection
- Limitations of Heritability Studies
- 25.5 Twin Studies Allow an Estimation of Heritability in Humans
- Large‐Scale Analysis of Twin Studies
- Twin Studies Have Several Limitations
- 25.6 Quantitative Trait Loci Are Useful in Studying Multifactorial Phenotypes
- Expression QTLs Regulate Gene Expression
- Expression QTLs and Genetic Disorders
- GENETICS, ETHICS, AND SOCIETY Rice, Genes, and the Second Green Revolution
- CASE STUDY A Chance Discovery
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 26 Population and Evolutionary Genetics
- 26.1 Genetic Variation Is Present in Most Populations and Species
- Detecting Genetic Variation
- Recombinant DNA Technology and Genetic Variation
- Genetic Variation in Genomes
- Explaining the High Level of Genetic Variation in Populations
- 26.2 The Hardy–Weinberg Law Describes Allele Frequencies and Genotype Frequencies in Population Ge
- Calculating Genotype Frequencies
- Calculating Allele Frequencies
- The Hardy–Weinberg Law and Its Assumptions
- 26.3 The Hardy–Weinberg Law Can Be Applied to Human Populations
- Testing for Hardy–Weinberg Equilibrium in a Population
- Calculating Frequencies for Multiple Alleles in Populations
- Calculating Allele Frequencies for X‐linked Traits
- Calculating Heterozygote Frequency
- 26.4 Natural Selection Is a Major Force Driving Allele Frequency Change
- Detecting Natural Selection in Populations
- Fitness and Selection
- There Are Several Types of Selection
- 26.5 Mutation Creates New Alleles in a Gene Pool
- 26.6 Migration and Gene Flow Can Alter Allele Frequencies
- 26.7 Genetic Drift Causes Random Changes in Allele Frequency in Small Populations
- Founder Effects in Human Populations
- 26.8 Nonrandom Mating Changes Genotype Frequency but Not Allele Frequency
- Inbreeding
- 26.9 Speciation Can Occur through Reproductive Isolation
- Changes Leading to Speciation
- The Rate of Macroevolution and Speciation
- 26.10 Phylogeny Can Be Used to Analyze Evolutionary History
- Constructing Phylogenetic Trees from DNA Sequences
- Reconstructing Vertebrate Evolution by Phylogenetic Analysis
- Molecular Clocks Measure the Rate of Evolutionary Change
- The Complex Origins of the Human Genome
- GENETICS ,ETHICS, AND SOCIETY Tracking Our Genetic Footprints out of Africa
- CASE STUDY A Tale of Two Olivias
- Summary Points
- Insights and Solutions
- Problems and Discussion Questions
- Extra‐Spicy Problems
- 26.1 Genetic Variation Is Present in Most Populations and Species
- CRISPR‐Cas and Genome Editing
- CRISPR‐Cas Is an Adaptive Immune System in Prokaryotes
- Discovery of CRISPR
- The CRISPR‐Cas Mechanism for RNA‐Guided Destruction of Invading DNA
- Type II CRISPR‐Cas Systems
- CRISPR‐Cas has been Adapted as a Powerful Tool for Genome Editing
- CRISPR‐Cas9 In Vitro
- CRISPR‐Cas9 Genome Editing of Mammalian Cells
- CRISPR‐Cas Infidelity
- CRISPR‐Cas Technology Has Diverse Applications
- CRISPR‐Cas as a Tool for Basic Genetic Research
- Box 1 The CRISPR‐Cas9 Patent Battle
- CRISPR‐Cas in Biotechnology
- Clinical Use of CRISPR‐Cas to Treat or Cure Disease
- Box 2 Ethical Concerns of Human Genome Editing
- CRISPR‐Cas Is an Adaptive Immune System in Prokaryotes
- DNA Forensics
- DNA Profiling Methods
- VNTR‐Based DNA Fingerprinting
- Box 1 The Pitchfork Case: The First Criminal Conviction Using DNA Profiling
- Autosomal STR DNA Profiling
- Y‐Chromosome STR Profiling
- Mitochondrial DNA Profiling
- Single‐Nucleotide Polymorphism Profiling
- DNA Phenotyping
- Box 2 Putting a Face to DNA: The Bouzigard Case
- Interpreting DNA Profiles
- The Uniqueness of DNA Profiles
- DNA Profile Databases
- Technical and Ethical Issues Surrounding DNA Profiling
- Box 3 The Kennedy Brewer Case: Two Bite‐Mark Errors and One Hit
- Box 4 A Case of Transference: The Lukis Anderson Story
- DNA Profiling Methods
- Genomics and Precision Medicine
- Pharmacogenomics
- Optimizing Drug Responses
- Developing Targeted Drugs
- Box 1 Preemptive Pharmacogenomic Screening: The PGEN4Kids Program
- Precision Oncology
- Targeted Cancer Immunotherapies
- Box 2 Precision Cancer Diagnostics and Treatments: The Lukas Wartman Story
- Box 3 Cell Types in the Innate and Adaptive Immune Systems
- Box 4 Steps in Cytotoxic T‐cell Recognition, Activation, and Destruction of Cancer Cells
- Precision Medicine and Disease Diagnostics
- Technical, Social, and Ethical Challenges
- Box 5 Beyond Genomics: Personal Omics Profiling
- Pharmacogenomics
- Genetically Modified Foods
- What Are GM Foods?
- Herbicide‐Resistant GM Crops
- Box 1 The Tale of GM Salmon—Downstream Effects?
- Insect‐Resistant GM Crops
- GM Crops for Direct Consumption
- Methods Used to Create GM Plants
- Selectable Markers
- Roundup‐Ready® Soybeans
- Golden Rice 2
- Gene Editing and GM Foods
- GM Foods Controversies
- Box 2 The New CRISPR Mushroom
- Health and Safety
- Environmental Effects
- The Future of GM Foods
- What Are GM Foods?
- Gene Therapy
- What Genetic Conditions Are Candidates for Treatment by Gene Therapy?
- How Are Therapeutic Genes Delivered?
- Viral Vectors for Gene Therapy
- Box 1 ClinicalTrials.gov
- Nonviral Delivery Methods
- Stem Cells for Delivering Therapeutic Genes
- The First Successful Gene Therapy Trial
- Gene Therapy Setbacks
- Problems with Gene Therapy Vectors
- Recent Successful Trials by Conventional Gene Therapy Approaches
- Treating Retinal Blindness
- Successful Treatment of Hemophilia B
- HIV as a Vector Shows Promise in Recent Trials
- Box 2 Glybera: The First Commercial Gene Therapy to be Approved in the West Lasted Only 5 Years
- Gene Editing Approaches to Gene Therapy
- DNA‐Editing Nucleases
- CRISPR‐Cas Method Revolutionizes Gene Editing Applications and Renews Optimism in Gene Therapy
- RNA‐Based Therapeutics
- Future Challenges and Ethical Issues
- Ethical Concerns Surrounding Gene Therapy
- Box 3 Gene Doping for Athletic Performance?
- Advances in Neurogenetics: The Study of Huntington Disease
- Box 1 George Huntington and His Namesake Disease
- The Search for the Huntington Gene
- Finding Linkage between Huntington Disease and an RFLP Marker
- Box 2 Nancy Wexler and the Venezuelan Pedigree
- Assigning the HD Gene to Chromosome 4
- The Identification and Cloning of the Huntington Gene
- Box 3 Genetic Testing for Huntington Disease
- The HTT Gene and Its Protein Product
- Molecular and Cellular Alterations in Huntington Disease
- Transcriptional Disruption
- Impaired Protein Folding and Degradation
- Synaptic Dysfunction
- Impaired Mitochondrial Function
- Transgenic Animal Models of Huntington Disease
- Using Transgenic Mice to Study Huntington Disease
- Transgenic Sheep as an Animal Model of Huntington Disease
- Cellular and Molecular Approaches to Therapy
- Stem Cells for Transplantation
- Identifying Potential Drugs for Therapy
- Gene Silencing to Reduce mHTT Levels
- Gene Editing in Huntington Disease
- The Relationship between HD and Other Neurodegenerative Disorders
- Box 4 Huntington Disease and Behavior
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