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Genetics: Analysis of Genes and Genomes: Analysis of Genes and Genomes 9th New edition [Mīkstie vāki]

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  • Formāts: Paperback / softback, 830 pages, weight: 1786 g
  • Izdošanas datums: 14-Dec-2017
  • Izdevniecība: Jones and Bartlett Publishers, Inc
  • ISBN-10: 128412293X
  • ISBN-13: 9781284122930
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  • Formāts: Paperback / softback, 830 pages, weight: 1786 g
  • Izdošanas datums: 14-Dec-2017
  • Izdevniecība: Jones and Bartlett Publishers, Inc
  • ISBN-10: 128412293X
  • ISBN-13: 9781284122930
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Genetics: Analysis of Genes and Genomes is a resource uniquely suited for learning and applying genetics to our world. Its DNA first presentation frames the discussion of genetics in modern terms, which provides the user the context to then understand its Mendelian history. Genetics continues to treat transmission genetics, molecular genetics, and evolutionary genetics as fully integrated subjects and provides students with an unprecedented understanding of the basic process of gene transmission, mutation, expression, and regulation. A new unit structure with self-contained chapters provides the flexibility to fit any course design, whether it be Mendel-early, Chromosome-early, or a Genome-first approach. The dynamism of genetics is also perfectly captured, as coverage of technological advances is woven together with ethical controversies.

Problem-solving is a core element to this experimental discipline, and the ninth edition of Genetics is unparalleled in the tools it provides to unlock this fascinating subject. This rich resource allows students copious opportunities to practice and learn by using the clearly-presented mathematical concepts and exercises and chapter problems that encourage students to analyze and apply new skills.
Preface xv
The Student Experience xvi
What's New in the Ninth Edition xxii
Teaching Tools xxvi
Acknowledgments xxviii
About the Authors xxxi
Unit I Defining and Working with GENES 1(80)
1 Genes, Genomes, and Genetic Analysis
2(38)
Learning Objectives & Science Competencies
3(1)
1.1 DNA as the Genetic Material
4(4)
Experimental Proof of the Genetic Function of DNA
4(2)
Genetic Role of DNA in Bacteriophages
6(2)
1.2 DNA Structure and Replication
8(3)
An Overview of DNA Replication
10(1)
1.3 Genes and Proteins
11(4)
Inborn Errors of Metabolism as a Cause of Hereditary Disease
12(3)
Roots Of Discovery: The Black Urine Disease
14(1)
1.4 Genetic Analysis
15(8)
Mutant Genes and Defective Proteins
16(3)
Roots Of Discovery: One Gene, One Enzyme
16(3)
Complementation Test for Mutations in the Same Gene
19(1)
Analysis of Complementation Data
20(2)
Other Applications of Genetic Analysis
22(1)
1.5 Gene Expression: The Central Dogma
23(5)
Transcription
24(1)
Translation
25(1)
The Genetic Code
26(2)
1.6 Mutation and Variation
28(2)
Variation in Populations
29(1)
1.7 Genes and Environment
30(1)
1.8 The Molecular Unity of Life
31(9)
Prokarya, Archaea, and Eukarya
32(1)
Genomes and Proteomes
32(8)
2 DNA Structure and Genetic Variation
40(41)
Learning Objectives & Science Competencies
41(1)
2.1 Genetic Differences Among Individuals
41(2)
DNA Markers as Landmarks in Chromosomes
41(2)
2.2 The Terminology of Genetic Analysis
43(1)
2.3 The Molecular Structure of DNA
44(7)
Polynucleotide Chains
44(2)
The Double Helix
46(1)
Base Pairing and Base Stacking
47(2)
Antiparallel Strands
49(1)
DNA Structure as Related to Function
50(1)
Roots Of Discovery: The Double Helix
51(1)
2.4 The Separation and Identification of Genomic DNA Fragments
51(7)
Restriction Enzymes and Site-Specific DNA Cleavage
52(2)
Gel Electrophoresis
54(2)
Nucleic Acid Hybridization
56(2)
2.5 Amplification of Specific DNA for Detection and Purification
58(6)
Constraints on DNA Replication: Primers and 5'-to-3' Strand Elongation
59(1)
The Polymerase Chain Reaction
60(4)
2.6 Types of DNA Markers Present in Genomic DNA
64(6)
Restriction Fragment Length Polymorphisms
64(1)
Single-Nucleotide Polymorphisms
64(3)
Tandem Repeat Polymorphisms
67(3)
The Cutting Edge: High-Throughput SNP Genotyping
68(2)
Copy-Number Variation
70(1)
2.7 Applications of DNA Markers
70(12)
Genetic Markers, Genetic Mapping, and "Disease Genes"
70(1)
Other Uses for DNA Markers
71(10)
Unit II Transmission Genetics 81(239)
3 Mendelian Genetics: The Principles of Segregation and Assortment
82(38)
Learning Objectives & Science Competencies
83(1)
3.1 Morphological and Molecular Phenotypes
83(2)
3.2 Segregation of a Single Gene
85(8)
Phenotypic Ratios in the F, Generation
87(1)
The Principle of Segregation
88(3)
Roots Of Discovery: What Did Gregor Mendel Think He Discovered?
90(1)
Verification of Segregation
91(1)
The Testcross and the Backcross
92(1)
3.3 Segregation of Two or More Genes
93(4)
The Principle of Independent Assortment
93(2)
The Testcross with Independently Assorting Genes
95(1)
Three or More Genes
95(2)
3.4 Human Pedigree Analysis
97(3)
Characteristics of Dominant and Recessive Inheritance
97(2)
Most Human Genetic Variation Is Not "Bad"
99(1)
Molecular Markers in Human Pedigrees
100(1)
3.5 Incomplete Dominance and Epistasis
100(7)
Roots Of Discovery: This Land Is Your Land
101(1)
Multiple Alleles
102(1)
Human ABO Blood Groups
103(2)
Epistasis
105(2)
3.6 Probability in Genetic Analysis
107(3)
Elementary Outcomes and Events
108(1)
Probability of the Union of Events
109(1)
Probability of the Intersection of Events
109(1)
3.7 Conditional Probability and Pedigrees
110(10)
'Bayes' Theorem
111(9)
4 The Chromosomal Basis of Inheritance
120(39)
Learning Objectives & Science Competencies
121(1)
4.1 The Stability of Chromosome Complements
121(2)
4.2 Mitosis
123(3)
Prophase
124(1)
Metaphase
124(2)
Anaphase
126(1)
Telophase
126(1)
4.3 Meiosis
126(10)
The First Meiotic Division: Reduction
129(6)
Roots Of Discovery: Grasshopper, Grasshopper
134(1)
The Second Meiotic Division: Equation
135(1)
4.4 Sex-Chromosome Inheritance
136(8)
Chromosomal Determination of Sex
136(1)
X-Linked Inheritance
136(4)
Roots Of Discovery: The White-Eyed Male
138(2)
Pedigree Characteristics of Human X-Linked Inheritance
140(1)
Heterogametic Females
141(1)
Nondisjunction as Proof of the Chromosome Theory of Heredity
141(1)
Sex Determination in Drosophila
142(2)
4.5 Probability in the Prediction of Progeny Distributions
144(3)
Using the Binomial Distribution in Genetics
145(1)
Meaning of the Binomial Coefficient
146(1)
4.6 Testing Goodness of Fit to a Genetic Hypothesis
147(12)
Random Variables and Distributions
147(1)
The Chi-Square Method
148(2)
Are Mendel's Data Too Good to Be True?
150(9)
5 Genetic Linkage and Chromosome Mapping
159(41)
Learning Objectives & Science Competencies
160(1)
5.1 Linkage and Recombination of Genes in a Chromosome
161(4)
Coupling Versus Repulsion of Syntenic Alleles
162(1)
The Chi-Square Test for Linkage
163(1)
Each Pair of Linked Genes Has a Characteristic Frequency of Recombination
164(1)
Recombination in Females Versus Males
165(1)
5.2 Genetic Mapping
165(11)
Map Distance and Frequency of Recombination
165(5)
Roots Of Discovery: Genes ALL in a Row
166(4)
Crossing Over
170(1)
Recombination Between Genes Results from a Physical Exchange Between Chromosomes
170(1)
Crossing Over Takes Place at the Four-Strand Stage of Meiosis
170(4)
Multiple Crossovers
174(2)
5.3 Genetic Mapping in a Three-Point Testcross
176(4)
Chromosome Interference in Double Crossovers
177(1)
Genetic Mapping Functions
178(1)
Genetic Map Distance and Physical Distance
179(1)
5.4 Mapping by Tetrad Analysis
180(4)
Unordered Tetrads
180(1)
Ordered Tetrads
181(3)
5.5 Genetic Mapping in Humans
184(6)
Inferring Linkage in Pedigrees
184(3)
Roots Of Discovery: Mapping Markers in the Human Genome
185(2)
Association Mapping
187(3)
5.6 Special Features of Recombination
190(10)
Recombination Within Genes
190(1)
Mitotic Recombination
190(10)
6 Human Karyotypes and Chromosome Behavior
200(45)
Learning Objectives & Science Competencies
201(1)
6.1 The Human Karyotype
201(12)
Standard Karyotypes
201(3)
The Centromere and Chromosome Stability
204(1)
Dosage Compensation of X-Linked Genes
205(3)
Roots Of Discovery: Lyonization of an X Chromosome
207(1)
The Calico Cat
208(1)
Pseudoautosomal Inheritance
208(1)
Active Genes in the "Inactive" X Chromosome
209(1)
Gene Content and Evolution of the Y Chromosome
209(4)
Roots Of Discovery: The First Human Chromosomal Disorder Identified
212(1)
6.2 Chromosome Abnormalities in Human Pregnancies
213(4)
Down Syndrome and Other Viable Trisomies
213(1)
Trisomic Segregation
214(1)
Sex-Chromosome Abnormalities
215(1)
Environmental Effects on Nondisjunction
216(1)
6.3 Chromosomal Deletions and Duplications
217(8)
Deletions
217(1)
Deletion Mapping
218(1)
Duplications
219(1)
Unequal Crossing Over in Human Red-Green Color Blindness
220(1)
Copy-Number Variation with Reciprocal Risks of Autism and Schizophrenia
221(3)
Gene Duplication and the Evolution of New Proteins
224(1)
6.4 Genetics of Chromosomal Inversions
225(2)
Paracentric Inversion (Not Including the Centromere)
226(1)
Pericentric Inversion (Including the Centromere)
227(1)
6.5 Chromosomal Translocations
227(5)
Reciprocal Translocations
227(1)
Pseudolinkage in Heterozygotes
228(2)
Robertsonian Translocations and Trisomy 21
230(1)
Translocation Complexes in Oenothera
230(2)
6.6 Genomic Position Effects on Gene Expression
232(1)
6.7 Polyploidy in Plant Evolution
233(12)
Sexual Versus Asexual Polyploidization
235(1)
Autopolyploids and Allopolyploids
236(2)
Monoploid Organisms
238(7)
7 The Genetic Basis of Complex Traits
245(34)
Learning Objectives & Science Competencies
246(1)
7.1 Complex Traits
246(4)
Continuous, Categorical, and Threshold Traits
247(1)
The Normal Distribution
247(2)
Reconciling Mendelian Inheritance with Continuous Traits
249(1)
7.2 Causes of Variation
250(6)
Roots Of Discovery: A Maize'n Grass
251(1)
Genotypic Variation
252(1)
Environmental Variation
253(1)
Genetics and Environment Combined
254(1)
Genotype-by-Environment Interaction and Association
255(1)
7.3 Heritability
256(3)
The Number of Genes Affecting Complex Traits
257(1)
Broad-Sense Heritability
258(1)
Narrow-Sense Heritability
258(1)
Twin Studies
258(1)
7.4 Correlation Between Relatives
259(3)
Covariance and Correlation
259(1)
The Graphical Meaning of a Correlation
260(2)
7.5 Heritability and Selection
262(4)
Phenotypic Change with Individual Selection: A Prediction Equation
262(2)
Long-Term Artificial Selection
264(1)
Heritabilities of Threshold Traits
264(2)
7.6 Misconceptions About Heritability
266(1)
7.7 Identification of Genes Affecting Complex Traits
267(12)
Linkage Analysis in the Genetic Mapping of Quantitative-Trait Loci
267(1)
Genome-Wide Association Studies
268(1)
Candidate Genes for Complex Traits
269(11)
The Cutting Edge: Crowd-Sourced Genomics
270(9)
8 Genetics of Bacteria and Their Viruses
279(41)
Learning Objectives & Science Competencies
280(1)
8.1 Plasmids and Genetic Exchange
280(2)
The F Plasmid: A Conjugative Plasmid
281(1)
8.2 Bacterial Genetics
282(3)
Mutant Phenotypes
282(1)
Isolating Auxotrophs
283(1)
Mechanisms of Genetic Exchange
284(1)
8.3 DNA-Mediated Transformation
285(1)
8.4 Genetic Exchange and Conjugation
286(8)
Cointegrate Formation and Hfr Cells
287(3)
Time-of-Entry Mapping
290(3)
F' Plasmids
293(1)
Roots Of Discovery: The Sex Life of Bacteria
293(1)
8.5 Transduction
294(3)
The Phage Lytic Cycle
294(1)
Generalized Transduction
294(3)
8.6 Bacteriophage Genetics
297(6)
Plaque Formation and Phage Mutants
297(1)
Genetic Recombination in the Lytic Cycle
298(1)
Fine Structure of the r// Gene in Bacteriophage T4
299(4)
8.7 Lysogeny and Specialized Transduction
303(17)
Site-Specific Recombination and Lysogeny
303(6)
Roots Of Discovery: Artoo
304(5)
Specialized Transduction
309(14)
The Cutting Edge: Surviving in a Hostile World
311(9)
Unit III Organization and Replication of Chromosomes and DNA
9 Molecular Organization of Chromosomes and Genomes
320(33)
Learning Objectives & Science Competencies
321(1)
9.1 Genome Size and Evolutionary Complexity: The C-Value Paradox
321(2)
9.2 The Supercoiling of DNA
323(2)
Topoisomerase Enzymes
324(1)
9.3 The Structure of Bacterial Genomes
325(3)
Mobile DNA in Prokaryotes
325(1)
Mobilization of Nonconjugative Plasmids
326(2)
9.4 The Structure of Eukaryotic Genomes
328(6)
The Nucleosome: The Structural Unit of Chromatin
328(1)
The Nucleosome Core Particle
328(3)
Chromosome Territories in the Nucleus
331(1)
Chromosome Condensation
332(1)
Polytene Chromosomes
333(1)
9.5 Analysis of Sequence Complexity in Eukaryotic Genomes
334(2)
Kinetics of DNA Renaturation
334(1)
Analysis of Genome Size and Repetitive Sequences by Renaturation Kinetics
335(1)
9.6 Unique and Repetitive Sequences in Eukaryotic Genomes
336(5)
Unique Sequences
337(1)
Highly Repetitive Sequences
337(1)
Middle-Repetitive Sequences and Transposable Elements
338(1)
Molecular Mechanisms of Transposition
338(2)
Transposable Elements in the Human Genome
340(1)
9.7 Molecular Structure of the Centromere
341(2)
9.8 Molecular Structure of the Telomere
343(10)
Roots Of Discovery: Telomeres: The Beginning of the End
346(1)
Telomere Length Limits the Number of Cell Doublings
346(7)
10 DNA Replication and Sequencing
353(29)
Learning Objectives & Science Competencies
354(1)
10.1 Problems of Initiation, Elongation, and Incorporation Error
354(1)
10.2 Semiconservative Replication of Double-Stranded DNA
355(6)
The Meselson-Stahl Experiment
355(2)
Theta Replication of Circular DNA Molecules
357(3)
Roots Of Discovery: Replication by Halves
358(2)
Rolling-Circle Replication
360(1)
10.3 Initiation of DNA Replication
361(2)
Unwinding, Stabilization, and Stress Release
361(1)
Formation of the Primosome Complex
362(1)
10.4 The Elongation Process and Proofreading
363(4)
Discontinuous Replication of the Lagging Strand
365(1)
The Joining of Precursor Fragments
366(1)
10.5 Terminating Replication
367(1)
10.6 Replication in Eukaryotes
367(5)
Semiconservative Replication of DNA in Chromosomes
368(1)
Multiple Origins and Bidirectional Replication in Eukaryotes
368(2)
Initiation
370(2)
Termination and the Problem of Telomeres
372(1)
10.7 Exploiting the System: DNA Sequencing
372(10)
Sanger Sequencing
373(1)
Next-Generation Sequencing
374(8)
11 Mutation, Repair, and Recombination
382(41)
Learning Objectives & Science Competencies
383(1)
11.1 Types of Mutations
383(2)
Germ-Line and Somatic Mutations
383(1)
Conditional Mutations
383(1)
Classification by Function
384(1)
11.2 The Molecular Basis of Mutation
385(7)
Nucleotide Substitutions
385(1)
Missense Mutations: The Example of Sickle-Cell Anemia
386(2)
Insertions, Deletions, and Frameshift Mutations
388(1)
Dynamic Mutation of Trinucleotide Repeats
389(2)
Cytosine Methylation and Gene Inactivation
391(1)
11.3 Transposable Elements as Agents of Mutation
392(1)
11.4 Spontaneous Mutation
393(4)
The Nonadaptive Nature of Mutation
394(1)
Estimation of Mutation Rates
395(1)
Hotspots of Mutation
395(2)
11.5 Mutagens
397(8)
Depurination
397(1)
Oxidation
398(1)
Base-Analog Mutagens
399(1)
Chemical Agents That Modify DNA
399(1)
Ultraviolet Irradiation
400(1)
Ionizing Radiation
401(2)
Genetic Effects of the Chernobyl Nuclear Accident
403(2)
Roots Of Discovery: X-Ray Daze
404(1)
11.6 Mechanisms of DNA Repair
405(6)
Mismatch Repair
405(2)
Base-Excision Repair
407(1)
AP Repair
408(1)
Nucleotide-Excision Repair
409(1)
Photoreactivation
409(1)
DNA Damage Bypass
409(1)
Double-Strand Gap Repair
410(1)
The SOS Repair System
411(1)
11.7 Reverse Mutations and Suppressor Mutations
411(3)
Intragenic Suppression
412(1)
Intergenic Suppression
412(1)
The Ames Test for Mutagen/Carcinogen Detection
413(1)
11.8 The Relationship Between Repair and Recombination
414(10)
Double-Strand Break and Repair Model
415(1)
Hotspots of Recombination
416(7)
Unit IV Gene Expression 423(226)
12 Molecular Biology of Gene Expression
424(42)
Learning Objectives & Science Competencies
425(1)
12.1 Amino Acids, Polypeptides, and Proteins
425(2)
12.2 Colinearity Between Coding Sequences and Polypeptides
427(1)
12.3 Overview of Transcription
428(1)
12.4 Transcription in Prokaryotes
429(4)
Initiation
429(2)
Genetic Evidence for Promoters
431(1)
Elongation
431(1)
Termination
432(1)
Roots Of Discovery: Messenger "Light"
432(1)
12.5 Transcription in Eukaryotes
433(3)
RNA Polymerases
433(1)
Promoters and Promoter Recognition
434(1)
Initiation
435(1)
Elongation
435(1)
Termination
436(1)
12.6 Messenger RNA and RNA Processing
436(7)
5' Capping and 3' Polyadenylation
437(1)
Splicing of Intervening Sequences
437(1)
Characteristics of Human Transcripts
437(1)
Coupling of Transcription and RNA Processing
438(1)
Mechanism of RNA Splicing
439(2)
Effects of Intron Mutations
441(1)
Exon Shuffling in the Origin of New Genes
442(1)
12.7 Protein Synthesis
443(8)
Initiation in Prokaryotes
443(2)
Initiation in Eukaryotes
445(1)
Elongation
445(2)
Release
447(1)
Translational Proofreading and Premature Termination
448(1)
Nonsense-Mediated Decay
449(1)
Polysomes
450(1)
12.8 Protein Folding and Chaperones
451(3)
Roots Of Discovery: Poly-U
453(1)
12.9 The Standard Genetic Code
454(12)
Genetic Evidence for a Triplet Code
454(2)
How the Code Was Cracked
456(1)
Features of the Standard Code
456(1)
Transfer RNA and Aminoacyl-tRNA Synthetase Enzymes
457(1)
Redundancy and Wobble
458(1)
Nonsense Suppression
458(8)
13 Molecular Mechanisms of Gene Regulation
466(53)
Learning Objectives & Science Competencies
467(1)
13.1 Transcriptional Regulation in Prokaryotes
467(3)
Inducible and Repressible Systems of Negative Regulation
468(1)
Positive Regulation
469(1)
Stochastic Noise in Gene Expression
469(1)
13.2 The Operon System of Gene Regulation
470(8)
Lac- Mutants
470(1)
Inducible and Constitutive Synthesis and Repression
470(1)
Repressors, Operators, and Promoters
471(1)
The Operon System of Transcriptional Regulation
472(1)
Stochastic Noise in Lac Expression
473(1)
Positive Regulation of the Lactose Operon
473(2)
Regulation of the Tryptophan Operon
475(3)
Roots Of Discovery: Operator? Operator?
476(2)
13.3 Regulation Through Transcription Termination
478(3)
Attenuation
478(3)
Riboswitches
481(1)
13.4 Regulation in Bacteriophage Lambda
481(3)
13.5 Transcriptional Regulation in Eukaryotes
484(13)
Galactose Metabolism in Yeast
484(2)
Transcriptional Activator Proteins
486(2)
Transcriptional Enhancers and Transcriptional Silencers
488(1)
Deletion Scanning
488(1)
The Eukaryotic Transcription Complex
489(2)
Chromatin-Remodeling Complexes
491(2)
Alternative Promoters
493(4)
13.6 Epigenetic Mechanisms of Transcriptional Regulation
497(2)
Cytosine Methylation
497(1)
Methylation and Transcriptional Inactivation
497(1)
Genomic Imprinting in the Female and Male Germ Lines
498(1)
13.7 Regulation Through RNA Processing and Decay
499(1)
Alternative Splicing
499(1)
Messenger RNA Stability
499(1)
13.8 Noncoding RNAs and Regulation
500(5)
Interfering RNAs
500(4)
Roots Of Discovery: Double Trouble
502(2)
Long Noncoding RNA
504(1)
13.9 Translational Control
505(2)
Regulatory RNAs Controlling Translation
506(1)
13.10 Programmed DNA Rearrangements
507(12)
Gene Amplification
507(1)
Antibody and T-Cell Receptor Variability
507(3)
Mating-Type Interconversion
510(1)
Transcriptional Control of Mating Type
511(8)
14 Manipulating Genes and Genomes
519(49)
Learning Objectives & Science Competencies
520(1)
14.1 Site-Specific DNA Cleavage and Cloning Vectors
521(3)
Production of DNA Fragments with Defined Ends
521(1)
Recombinant DNA Molecules
522(1)
Plasmid, Lambda, and Cosmid Vectors
522(2)
14.2 Cloning Strategies
524(4)
Joining DNA Fragments
524(2)
Insertion of a Particular DNA Molecule into a Vector
526(1)
The Use of Reverse Transcriptase: cDNA and RT-PCR
526(2)
14.3 Detection of Recombinant Molecules
528(3)
Gene Inactivation in the Vector Molecule
528(2)
Screening for Particular Recombinants
530(1)
14.4 Genomics
531(7)
Genomic Sequencing
531(1)
Sequencing the Human Genome
532(1)
Genome Annotation
533(2)
Comparative Genomics
535(3)
14.5 Functional Genomics
538(9)
Chromatin Immunoprecipitation
543(1)
Two-Hybrid Analysis of Protein-Protein Interactions
544(3)
14.6 Transgenic Organisms
547(8)
Germ-Line Transformation in Animals
547(4)
Roots Of Discovery: Hello, Dolly!
548(3)
Genetic Engineering in Plants
551(1)
Transformation Rescue
552(1)
Site-Directed Mutagenesis and Knockout Mutations
553(1)
Gene Expression "Knockdown" with RNAi
554(1)
14.7 Gene Editing
555(4)
CRISPR-Casg in Practice
555(4)
The Cutting Edge: Editing the Muscular Dystrophy Gene
557(2)
14.8 Some Applications of Genetic Engineering
559(9)
Giant Salmon with Engineered Growth Hormone
559(1)
Nutritionally Engineered Rice
559(1)
Production of Useful Proteins
560(1)
Genetic Engineering with Animal Viruses
560(8)
15 Genetic Control of Development
568(41)
Learning Objectives & Science Competencies
569(1)
15.1 Genetic Determinants of Development
569(1)
15.2 Early Embryonic Development in Animals
570(4)
Autonomous Development and Intercellular Signaling
570(1)
Composition and Organization of Oocytes
571(2)
Early Development and Activation of the Zygotic Genome
573(1)
15.3 Genetic Analysis of Development in the Nematode
574(8)
Analysis of Cell Lineages
574(2)
Roots Of Discovery: Distinguished Lineages
575(1)
Mutations Affecting Cell Lineages
576(1)
Programmed Cell Death
576(1)
Loss-of-Function and Gain-of-Function Alleles
576(3)
Epistasis in the Analysis of Developmental Switches
579(3)
15.4 Genetic Control of Development in Drosophila
582(13)
Maternal-Effect Genes and Zygotic Genes
584(1)
Genetic Basis of Pattern Formation in Early Development
585(1)
Coordinate Genes
586(3)
Roots Of Discovery: Embryogenesis
588(1)
Gap Genes
589(1)
Pair-Rule Genes
589(1)
Segment-Polarity Genes
590(1)
Interactions in the Regulatory Hierarchy
590(2)
Metamorphosis of the Adult Fly
592(1)
Homeotic Genes
592(1)
Master Control Genes in Evolution
593(2)
15.5 Regulatory RNAs in Development
595(3)
Micro RNA-Based Regulation in C. elegans
595(1)
miRNAs in HOX Gene Regulation
596(1)
Long Intergenic Noncoding RNAs
597(1)
15.6 Genetic Control of Development in Higher Plants
598(11)
Flower Development in Arabidopsis
599(1)
Combinatorial Determination of the Floral Organs
600(9)
16 Molecular Genetics of the Cell Cycle and Cancer
609(40)
Learning Objectives & Science Competencies
610(1)
16.1 The Cell Cycle
610(3)
Key Events in the Cell Cycle
610(2)
Transcriptional Program of the Cell Cycle
612(1)
16.2 Genetic Analysis of the Cell Cycle
613(2)
Mutations Affecting Progression Through the Cell Cycle
613(2)
16.3 Progression Through the Cell Cycle
615(6)
Cyclins and Cyclin-Dependent Protein Kinases
615(3)
Roots Of Discovery: Cycle-Ops
617(1)
Targets of the Cyclin-CDK Complexes
618(1)
Triggers for the Gi/S and G2/M Transitions
618(2)
Protein Degradation Helps Regulate the Cell Cycle
620(1)
16.4 Checkpoints in the Cell Cycle
621(5)
The DNA Damage Checkpoint
622(3)
The Centrosome Duplication Checkpoint
625(1)
The Spindle Assembly Checkpoint
625(1)
Consequences of Checkpoint Failure
625(1)
16.5 Cancer Cells
626(5)
Oncogenes and Proto-oncogenes
627(1)
Tumor-Suppressor Genes
628(3)
16.6 Hereditary Cancer Syndromes
631(5)
Defects in DNA Repair
634(3)
Roots Of Discovery: Two Hits, Two Errors
635(1)
16.7 Genetics of the Acute Leukemias
636(1)
16.8 The Genomics and Transcriptomics of Cancer
637(13)
Pancreatic Cancer: The Mutational Landscape
638(3)
Pancreatic Cancer: The Transcriptiosomal Landscape
641(1)
From Genes and Transcripts to Therapy?
641(8)
Unit V Variation 649(110)
17 Mitochondrial DNA and Extranuclear Inheritance
650(27)
Learning Objectives & Science Competencies
651(1)
17.1 Origin and Molecular Genetics of Organelles
651(4)
Organelle Genomes
652(1)
RNA Editing
652(1)
The Genetic Codes of Organelles
653(2)
Roots Of Discovery: A Coming Together
654(1)
17.2 Patterns of Extranuctear Inheritance
655(9)
Maternal Inheritance of Animal Mitochondria
655(1)
Maternal Inheritance and Maternal Effects
656(1)
Heteroplasmy
656(8)
17.4 Cytoplasmic Transmission of Symbionts
664(6)
Bacterial Symbionts of Aphids
665(1)
Roots Of Discovery: How the Aphids Got PVT
665(1)
Killer Strains of Paramecium
666(1)
Wolbachia in Arthropods
667(3)
17.5 Maternal Effect in Snail Shell Coiling
670(7)
18 Genes in Populations
677(40)
Learning Objectives & Science Competencies
678(1)
18.1 Population Genetics
678(13)
Allele Frequencies and Genotype Frequencies
678(2)
Random Mating and the Hardy-Weinberg Principle
680(1)
Implications of the Hardy-Weinberg Principle
681(1)
A Test for Random Mating
681(1)
Frequency of Heterozygous Genotypes
682(1)
Multiple Alleles
683(1)
DNA Typing
684(4)
X-Linked Genes
688(1)
Genetic Variation and Linkage
688(3)
18.2 Inbreeding
691
The Inbreeding Coefficient
691(1)
Allelic Identity by Descent
692(1)
Calculation of the Inbreeding Coefficient from Pedigrees
693
Mitochondrial Genetic Diseases
657(1)
Tracing Population History Through Mitochondrial DNA
658(1)
Cytoplasmic Male Sterility in Plants
659(2)
17.3 Vegetative Segregation
661(34)
Leaf Variegation in Four-O'Clock Plants
661(2)
Respiration-Defective Mitochondrial Mutants in Yeast
663(31)
Roots Of Discovery: A Yule Message from Dr. Hardy
684(10)
Effects of Inbreeding
694(1)
18.3 Genetics and Evolution
695(1)
18.4 Mutation and Migration
696(2)
Irreversible Mutation
696(1)
Reversible Mutation
697(1)
18.5 Random Genetic Drift
698(3)
Loss of Genetic Variation in Endangered Species
699(2)
18.6 Natural Selection
701(16)
Selection in a Laboratory Experiment
701(1)
Selection in Diploid Organisms
702(1)
Components of Fitness
703(1)
Selection-Mutation Balance
704(1)
Heterozygote Superiority
705(1)
Molecular Signals of Selection
706(12)
The Cutting Edge: CRISPR-Casg for Disease Control?
708(9)
19 Molecular and Human Evolutionary Genetics
717(42)
Learning Objectives & Science Competencies
718(1)
19.1 Molecular Evolutionary Analysis
718(9)
Gene Trees
719(2)
Bootstrapping
721(1)
Gene Trees and Species Trees
721(1)
Molecular Clock of Evolutionary Change
722(1)
Rates of DNA Evolution
723(1)
Rates of Evolution in Protein-Coding Regions
724(2)
Origins of New Genes: Orthologs and Paralogs
726(1)
19.2 Ancient DNA
727(2)
19.3 Where Humans Fit on the Tree of Life
729(3)
Evidence That Humans Are Most Closely Related to Chimpanzees
729(1)
Similarities in Genomic DNA
729(1)
Analysis of Multiple Genetic Elements
729(1)
Differences Between Human and Chimpanzee Genomes
730(2)
19.4 What Do the Genetic Differences Between Humans and Chimpanzees Mean?
732(3)
Molecular Adaptations Unique to Humans
732(1)
FOXP2: A Gene Related to Language
733(1)
Gene-Expression Differences Between Humans and Chimpanzees
734(1)
19.5 A Synopsis of Human Evolution
735(4)
The Cast of Characters in Human Evolution
735(3)
Models of Modern Human Origins
738(1)
19.6 Genetic Evidence for Modern Human Origins
739(4)
Tracing Human History Through Mitochondria) DNA
739(2)
The Neandertal Genome
741(1)
The Denisovan Genome
742(1)
19.7 Measuring Human Diversity
743(6)
Tracing Human History with Genetic Markers
743(3)
The Apportionment of Within-Group and Between-Group Variation
746(1)
Tracing Human History Through the Y Chromosome
746(3)
The Cutting Edge: The Peopling of Western Europe
747(2)
19.8 Genetic Adaptations Unique to Humans
749(10)
Amylase and Dietary Starch
749(2)
Roots Of Discovery: Starch Contrast
750(1)
Adaptation to Parasites and Disease
751(1)
Evolutionary Adaptation Affecting Human Skin Color
752(7)
Appendix A: Answers to Even-Numbered Problems 759(49)
Word Roots: Prefixes, Suffixes, and Combining Forms
778(3)
Concise Dictionary of Genetics and Genomics
781(27)
Index 808
Daniel L. Hartl is Higgins Professor of Biology at Harvard University, a Professor of Immunology and Infectious Diseases at the Harvard T. H. Chan School of Public Health, and a Senior Associate Member of the Broad Institute of M.I.T. and Harvard. He is a member of the National Academy of Sciences and the American Academy of Arts and Sciences. He received his B.S. degree and Ph.D. from the University of Wisconsin and carried out postdoctoral research at the University of California at Berkeley. His research interests include molecular genetics, genomics, molecular evolution, and population genetics

Miami University, Oxford, Ohio