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© 2012 Pearson Education, Inc. Lecture by Edward J. Zalisko PowerPoint Lectures for Campbell Biology: Concepts & Connections, Seventh Edition Reece, Taylor,

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Presentation on theme: "© 2012 Pearson Education, Inc. Lecture by Edward J. Zalisko PowerPoint Lectures for Campbell Biology: Concepts & Connections, Seventh Edition Reece, Taylor,"— Presentation transcript:

1 © 2012 Pearson Education, Inc. Lecture by Edward J. Zalisko PowerPoint Lectures for Campbell Biology: Concepts & Connections, Seventh Edition Reece, Taylor, Simon, and Dickey Chapter 12 DNA Technology and Genomics

2 GENOMICS © 2012 Pearson Education, Inc.

3 12.17 Genomics is the scientific study of whole genomes  Genomics is the study of an organism’s complete set of genes and their interactions.  The goals of the Human Genome Project (HGP) included –determining the nucleotide sequence of all DNA in the human genome and –identifying the location and sequence of every human gene.  Why sequence so many genomes from other organisms?  Comparative genomics allows another way to examine evolutionary relationships. –Genomic studies showed a 96% similarity in DNA sequences between chimpanzees and humans. –Functions of human disease-causing genes have been determined by comparing human genes to similar genes in yeast. © 2012 Pearson Education, Inc.

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6 Figure 12.19 Chromosome Chop up each chromosome with restriction enzymes Sequence the fragments DNA fragments Align the fragments Reassemble the full sequence

7 12.18 The Human Genome Project revealed that most of the human genome does not consist of genes  Results of the Human Genome Project indicate that –humans have about 20,000 genes in 3.2 billion nucleotide pairs, –only 1.5% of the DNA codes for proteins, tRNAs, or rRNAs, and –the remaining 98.5% of the DNA is noncoding DNA © 2012 Pearson Education, Inc.

8 Figure 12.18 Exons (regions of genes coding for protein or giving rise to rRNA or tRNA) (1.5%) Repetitive DNA that includes transposable elements and related sequences (44%) Introns and regulatory sequences (24%) Unique noncoding DNA (15%) Repetitive DNA unrelated to transposable elements (15%)

9 Functions of the Eukaryotic Genome

10 Genomes hold clues to human evolution  Human and chimp genomes differ by –1.2% in single-base substitutions and –2.7% in insertions and deletions of larger DNA sequences.  Genes showing rapid evolution in humans include –genes for defense against malaria and tuberculosis, –a gene regulating brain size, and –the FOXP2 gene involved with speech and vocalization. © 2012 Pearson Education, Inc.

11 DNA Testing and Analyzing DNA Sequence Differences © 2012 Pearson Education, Inc.

12 12.2 Enzymes are used to “cut and paste” DNA  Restriction enzymes cut DNA at specific sequences. –Each enzyme binds to DNA at a different restriction site. © 2012 Pearson Education, Inc. Animation: Restriction Enzymes

13 Bacteria Fight Invading Viruses by Making Restriction Enzymes

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15 12.12 The PCR method is used to amplify DNA sequences  Polymerase chain reaction (PCR) is a method of amplifying a specific segment of a DNA molecule.  The advantages of PCR include –the ability to amplify DNA from a small sample, –obtaining results rapidly, and –a reaction that is highly sensitive, copying only the target sequence. © 2012 Pearson Education, Inc.

16 12.13 Gel electrophoresis sorts DNA molecules by size  Gel electrophoresis can be used to separate DNA molecules based on size as follows: 1.A DNA sample is placed at one end of a porous gel. 2.DNA molecules move toward the positive electrode. 3.Shorter DNA fragments move through the gel matrix more quickly and travel farther through the gel. 4.Each band is a collection of DNA molecules of the same length. © 2012 Pearson Education, Inc. Video: Biotechnology Lab

17 Figure 12.UN02 A mixture of DNA fragments A “band” is a collection of DNA fragments of one particular length Longer fragments move slower Shorter fragments move faster DNA is attracted to  pole due to PO 4  groups Power source

18 Figure 12.13_1 A mixture of DNA fragments of different sizes Power source Gel Completed gel Longer (slower) molecules Shorter (faster) molecules

19 12.16 RFLPs can be used to detect differences in DNA sequences  A single nucleotide polymorphism (SNP) is a variation at a single base pair within a genome.  Restriction fragment length polymorphism (RFLP) is a change in the length of restriction fragments due to a SNP that alters a restriction site.  RFLP analysis involves –producing DNA fragments by restriction enzymes and –sorting these fragments by gel electrophoresis. © 2012 Pearson Education, Inc.

20 Figure 12.16 Restriction enzymes added DNA sample 1DNA sample 2 Cut w x yy z Sample 1 Sample 2 z x w yy Longer fragments Shorter fragments

21 DNA is isolated. 1 2 3 The DNA cut With restriction enzymes Restriction Fragment patterns are compared. Crime sceneSuspect 1Suspect 2 RFLP Analysis Can be Used for Forensics

22 RFLP Analysis to Detect Genetic Disorder SCA

23 Child Child Child Cntrl Dad A B C (no mutation) (has mutation)


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