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

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© 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

GENOMICS © 2012 Pearson Education, Inc.

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.

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

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.

Figure 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%)

Functions of the Eukaryotic Genome

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.

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

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

Bacteria Fight Invading Viruses by Making Restriction Enzymes

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.

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

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

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

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.

Figure 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

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

RFLP Analysis to Detect Genetic Disorder SCA

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