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Biotechnology Chapter 10 10.1 Impacts/Issues Golden Rice or Frankenfood? Genes from one species may be inserted into an individual of another species – or a gene may be modified and reinserted into an individual of the same species Golden Rice Rice plants with added genes make and store beta carotene Video: Golden rice or Frankenfood? GMOs and Transgenic Organisms Transgenic • An organism that has been genetically modified with genes from a different species Genetically modified organisms (GMOs) • Organism whose genome has been modified by genetic engineering 10.2 Finding Needles in Haystacks Gene research was limited until enzymes produced by bacteria to cut viral DNA were discovered Restriction enzyme • Enzyme that cuts DNA at specific base sequences • Used in DNA cloning to cut DNA into pieces that are inserted into cloning vectors DNA Cloning DNA cloning mass-produces DNA fragments for research DNA cloning • Set of procedures that uses living cells to make many identical copies of a DNA fragment Clone • A genetically identical copy of DNA, a cell, or an organism Cloning Vectors Cloning vector • A DNA molecule that can accept foreign DNA, resulting in a hybrid molecule that can be transferred to a host cell, and get replicated in it Plasmid • A small, circular DNA molecule in bacteria, replicated independently of the chromosomes • A cloning vector Recombinant DNA Recombinant DNA molecules are introduced into host cells such as bacteria, which copy the DNA as they divide Recombinant DNA • Contains genetic material from more than one organism Making Recombinant DNA 1. A restriction enzyme recognizes specific base sequences in DNA from two different sources 2. Restriction enzymes cut DNA into fragments with single-stranded tails (“sticky ends”) 3. DNA fragments from different sources are mixed together; matching sticky ends base-pair 4. DNA ligase joins fragments, forming recombinant DNA Making Recombinant DNA restriction enzyme (cut) 1 A restriction enzyme recognizes a specific base sequence in DNA (green boxes) from two sources. mix 2 The enzyme cuts DNA from both sources into fragments that have sticky ends. DNA ligase (paste) 3 The DNA fragments from the two sources are mixed together. The matching sticky ends base-pair with each other. 4 DNA ligase joins the fragments of DNA where they overlap. Molecules of recombinant DNA are the result. Stepped Art Fig. 10-2, p. 181 Commercial Plasmid Cloning Vector Kpn l Sph l Pst l Bam Hl Eco RI Sal l pDrive Cloning Vector 3.85 kb Acc l Xho l Xba l Bst XI Sac l Not l Fig. 10-3, p. 181 cDNA Cloning RNA cannot be cloned directly; reverse transcriptase is used to copy single-stranded RNA into cDNA for cloning Reverse transcriptase • Viral enzyme that uses mRNA as a template to make a strand of DNA cDNA • DNA synthesized from an RNA template by the enzyme reverse transcriptase Making cDNA mRNA A The enzyme reverse transcriptase transcribes mRNA into DNA. mRNA cDNA B DNA polymerase replicates the DNA strand. cDNA cDNA Eco RI recognition site C The result is a double-stranded molecule of DNA that can be cut and pasted into a cloning vector. Fig. 10-4, p. 182 mRNA A The enzyme reverse transcriptase transcribes mRNA into DNA. mRNA cDNA B DNA polymerase replicates the DNA strand. cDNA cDNA Eco RI recognition site C The result is a double-stranded molecule of DNA that can be cut and pasted into a cloning vector. Stepped Art Fig. 10-4, p. 182 Libraries A library is a collection of cells that host different fragments of DNA, often representing an organism’s entire genome Researchers make DNA libraries to isolate one gene from the many other genes in a genome Genome • An organism’s complete set of genetic material Nucleic Acid Hybridization Probes are used to identify one clone that hosts a DNA fragment of interest among many other clones in a DNA library Probe • Short fragment of DNA labeled with a tracer • Hybridizes with a specific nucleotide sequence Nucleic acid hybridization • Base-pairing between DNA or RNA from different sources PCR PCR quickly mass-produces copies of a particular DNA fragment for study Polymerase chain reaction (PCR) • Uses primers and heat-resistant DNA polymerase to rapidly generate many copies of a DNA fragment Primer • Short, single-strand of DNA designed to hybridize with a DNA fragment Steps in PCR 1. Starting material is mixed with DNA polymerase, nucleotides and primers 2. Mixture is heated and cooled in cycles • At high temperature, DNA unwinds • At low temperature, primers base-pair with template DNA 3. Taq polymerase synthesizes complementary DNA strands on templates Two Rounds of PCR 1 DNA template (blue) is mixed with primers (red), nucleotides, and heattolerant Taq DNA polymerase. 2 When the mixture is heated, the double-stranded DNA separates into single strands. zhen it is cooled, some of the primers base-pair with the template DNA. 3 Taq polymerase begins DNA synthesis at the primers, and complementary strands of DNA form on the single-stranded templates. 4 The mixture is heated again, and the double-stranded DNA separates into single strands. When it is cooled, some of the primers base-pair with the template DNA. 5 Taq polymerase begins DNA synthesis at the primers, and complementary strands of DNA form on the single-stranded templates. Fig. 10-5, p. 183 1 DNA template (blue) is mixed with primers (red), nucleotides, and heattolerant Taq DNA polymerase. 22When Whenthe themixture mixtureisisheated, heated,the the double-stranded double-strandedDNA DNAseparates separatesinto into single singlestrands. strands.When Whenititisiscooled, cooled, some someofofthe theprimers primersbase-pair base-pairwith withthe the template templateDNA. DNA. 44The Themixture mixtureisisheated heatedagain, again, and andthe thedouble-stranded double-strandedDNA DNA separates separatesinto intosingle singlestrands. strands.When When ititisiscooled, cooled,some someofofthe theprimers primers base-pair base-pairwith withthe thetemplate templateDNA. DNA. 3 Taq polymerase begins DNA synthesis at the primers, and complementary strands of DNA form on the single-stranded templates. 5 Taq polymerase begins DNA synthesis at the primers, and complementary strands of DNA form on the single-stranded templates. Stepped Art Fig. 10-5, p. 183 Animation: Polymerase chain reaction (PCR) Animation: Formation of recombinant DNA Animation: Use of a radioactive probe Animation: Base-pairing of DNA fragments Animation: How to make cDNA Animation: Restriction enzymes Animation: F2 ratios interaction 10.3 Studying DNA Short tandem repeats are multiple copies of a short DNA sequence that follow one another along a chromosome The number and distribution of short tandem repeats, unique in each individual, is revealed by electrophoresis as a DNA fingerprint DNA Fingerprinting DNA fingerprinting is used in forensics, court evidence, and other applications DNA fingerprint • An individual’s unique array of short tandem repeats Electrophoresis • Used to separate DNA fragments by size DNA Fingerprinting: A Forensic Case Suspect 2 Female Cells Semen Size Reference Boyfriend Control DNA Control DNA Size Reference Control DNA Size Reference Victim Suspect 1 Size Reference Evidence from Crime Scene Fig. 10-6, p. 184 The Human Genome Project Automated DNA sequencing and PCR enabled scientists to sequence the more than 3 billion bases of the human genome Sequencing • Method of determining the order of nucleotides in DNA Sequencing a Fragment of DNA The order of colors is the order of DNA bases (A, T, G, C) Genomics Analysis of the human genome sequence is yielding new information about human genes and how they work Genomics • The study of genomes (structural genomics, comparative genomics) Some Sequenced Genomes Animation: Automated DNA sequencing Animation: DNA fingerprinting Video: ABC News: DNA mystery: Human chimeras Video: ABC News: Family ties: Paternity testing 3D Animation: Gene sequencing 10.4 Genetic Engineering Recombinant DNA technology and genome analysis are the basis of genetic engineering Genetic engineering is the directed alteration of an individual’s genome, resulting in a genetically modified organism (GMO) Genetic engineering • Process by which deliberate changes are introduced into an individual’s genome Genetically Modified Microorganisms A transgenic organism carries a gene from a different species Transgenic organisms are used in research, medicine, and industry Transgenic bacteria and yeast produce medically valuable proteins Designer Plants Transgenic crop plants help farmers produce food more efficiently Plants with modified or foreign genes are now common in farm crops Using the Ti plasmid to Make a Transgenic Plant 1 An A. tumefaciens bacterium has been engineered to contain a Ti plasmid. The plasmid carries a foreign gene. 2 The bacterium infects a plant cell and transfers the Ti plasmid into it. The plasmid DNA becomes integrated into one of the cell’s chromosomes. 3 The plant cell divides, and its descendants form an embryo. 4 The embryo develops into a transgenic plant. 5 The transgenic plant expresses the foreign gene. This tobacco plant is expressing a gene from a firefly. Fig. 10-8, p. 187 Animation: Gene transfer using a Ti plasmid Genetically Modified Crops Bt gene confers insect resistance to corn Biotech Barnyards Transgenic animals produce human proteins Animals that would be impossible to produce by traditional breeding methods are being created by genetic engineering Transgenic animals are used in research, medicine, and industry Transgenic Animals Knockout Cells and Organ Factories Transgenic animals may one day provide a source of organs and tissues for transplantation into humans Xenotransplantation • Transplant of an organ from one species to another Animation: Transferring genes into plants Video: ABC News: Cloned pooch Video: ABC News: Mule clones Video: ABC News: Glow-in-the-dark pigs Video: ABC News: Cloned food approved 10.5 Genetically Modified Humans Genes can be transferred into a person’s cells to correct a genetic defect or treat a disease However, the outcome of altering a person’s genome remains unpredictable Gene therapy • Transfer of a normal or modified gene into an individual with the goal of treating a genetic defect or disorder Unpredictable Outcomes There are more than 15,000 serious genetic disorders – gene therapy is the only real cure In some cases, gene therapy works – in other cases it leads to death • Inserting a virus-injected gene into a chromosome can disrupt normal function and cause cancer • Severe allergic reaction to the viral vector can cause death One Successful Case of Gene Therapy Rhys Evans, born with a severe immune disorder (SCID-X1) received a normal gene and no longer lives in isolation Getting Perfect Eugenics • Idea of deliberately improving the genetic qualities of the human race The potential benefits of genetically modifying humans must be weighed against the potential risks, including social implications 10.6 Impacts/Issues Revisited Golden rice with beta carotene was ready for distribution in 2005 but is still not available for human consumption – the biosafety experiments required are too expensive for the public humanitarian agency that developed it Digging Into Data: Enhanced Spatial Learning in Mice With Autism Mutation Fig. 10-11a, p. 193 Fig. 10-11b, p. 193