Recombinant DNA: Genes and Genomes: A Short Course

Front Cover
Macmillan, 2007 - Medical - 474 pages
Recombinant DNA, Third Edition, is an essential text for undergraduate, graduate, and professional courses in Genomics, Cell and Molecular Biology, Recombinant DNA, Genetic Engineering, Human Genetics, Biotechnology, and Bioinformatics. The Third Edition of this landmark text offers an authoritative, accessible, and engaging introduction to modern, genome-centered biology from its foremost practitioners. The new edition explores core concepts in molecular biology in a contemporary inquiry-based context, building its coverage around the most relevant and exciting examples of current research and landmark experiments that redefined our understanding of DNA. As a result, students learn how working scientists make real high-impact discoveries. The first chapters provide an introduction to the fundamental concepts of genetics and genomics, an inside look at the Human Genome Project, bioinformatic and experimental techniques for large-scale genomic studies, and a survey of epigenetics and RNA interference. The final chapters cover the quest to identify disease-causing genes, the genetic basis of cancer, and DNA fingerprinting and forensics. In these chapters the authors provide examples of practical applications in human medicine, and discuss the future of human genetics and genomics projects.
 

Contents

SECTION
1
3 polyA Tails and 5 Methylguanosine
3
Genes Are Mapped on Chromosomes Using Linkage
7
Quantitating DNA Bases in Different Organisms Hints at Unlimited
14
Information Flow from DNA to Protein
29
Control of Gene Expression
53
Eukaryotic Transcription and Gene
62
Basic Tools of Recombinant DNA
75
FOUNDATIONS OF GENOMICS
247
Doublestranded RNA Is the Trigger
253
Longer Sequences Are Put Together
264
How the Human Genome Was Sequenced
273
Comparative Sequence Analysis Shows That
282
ANALYZING GENOMES
309
Comparative Genomics Helps to Identify
329
From Genome Sequence to Gene Function
335

Fundamental Features of Eukaryotic Genes
107
Caps Are Added to the Ends
121
Southern and Northern Blotting Procedures
126
A New Toolbox for Recombinant DNA
129
Mobile DNA Sequences in the Genome
159
Epigenetic Modifications of the Genome
189
The Gene Xist Its Complement Tsix
196
Not All Genes on the Mammalian X
197
Imprinting Must Be Correct for the Proper
210
RNA Interference Regulates Gene Action
219
mRNA Levels Are Also Measured
343
Arrayed Antibodies Are Used to Measure
356
HUMAN GENOMICS
365
Pharmacogenomic Strategy Leads
387
Understanding the Genetic Basis of Cancer
395
DNA Fingerprinting and Forensics
431
Familial Searches Identify Suspects
449
Figure Credits
459
Copyright

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About the author (2007)

James D. Watson, co-winner of the Nobel prize for discovering the DNA double helix, is Chancellor of the Cold Spring Harbor Laboratory. Jan A. Witkowski is Executive Director of the Banbury Center and Professor in the Watson School of Biological Sciences at Cold Spring Harbor Laboratory. Richard M. Myers is Chairman and Stanford W. Ascherman Professor in the Department of Genetics at Stanford University, and is Director of the Stanford Human Genome Center. Amy A. Caudy is the Lewis-Stiger Fellow at the Lewis-Stiger Institute for Integrative Genomics at Princeton University.