1. DNA Technologies

2. Biotechnology Dolly and surrogate Mom Genetically modified rice. Embryonic stem cells and gene therapy

3. Biotechnology Biotechnology, defined broadly, is the engineering of organisms for useful purposes. Often, biotechnology involves the creation of hybrid genes and their introduction into organisms in which some or all of the gene is not normally present. Fourteen month-old genetically engineered (“biotech”) salmon (left) and standard salmon (right).

4. DNA Technology  DNA technology is the chemical manipulation of the genotypes and resulting phenotypes of organisms such that living organisms are modified  Alternatively, no-longer-living organisms or their no- longer-living parts may be analyzed chemically at the level of genotype  DNA technology has revolutionized how scientists study the genetics, biochemistry, even the ecology and evolutionary biology of organisms  Genetic engineering is the artificial manipulation of the genetic material of organisms, including the creation of novel genetic material (i.e., novel nucleotide sequences)  Biotechnology is the development of novel biological products, indeed whole industries are now devoted to the production and analysis of biological materials

5. Biotechnology We’ll examine: Animal cloning Gene cloning for pharmaceutical production The promise and perhaps perils of embryonic stem cells DNA fingerprinting Genetically modified foods and the American- European opinion divide.

6. Animal Cloning Dolly and her surrogate mother.

7. Why Clone Animals? To answer questions of basic biology Five genetically identical cloned pigs. For herd improvement.To satisfy our desires (e.g. pet cloning). For pharmaceutical production.

8. Is Animal Cloning Ethical? The first cloned horse and her surrogate mother/genetic twin. As with many important questions, the answer is beyond the scope of science.

9. USU’s Contribution – A Cloned Mule and the First Cloned Equine

10. The Biotechnology of Reproductive Cloning Even under the best of circumstances, the current technology of cloning is very inefficient. Cloning provides the most direct demonstration that all cells of an individual share a common genetic blueprint.

11. Saved by Cloning? Some are firm believers while many view these approaches to be more of a stunt. Note the use of a closely related species, a domestic goat, as egg donor and surrogate mother.

12. (Science (2002) 295:1443) Carbon Copy– the First Cloned Pet Significantly, Carbon Copy is not a phenotypic carbon copy of the animal she was cloned from.

13. The Next Step? Highly unlikely. Attempts at human cloning are viewed very unfavorably in the scientific community.

14. So how do we do all of this???

15. Recombinant DNA methods  Restriction enzymes Enzymes from bacteria Used to cut DNA molecules in specific places Enable researchers to cut DNA into manageable segments  Vector -molecule carrier of DNA fragment into cell  Transformation: uptake of foreign DNA into cells

16. Cutting DNA with a restriction enzyme

17. Restriction Enzymes

18. Restriction Endonucleases A Restriction Endonucleases will cut both strands of a DNA duplex at a specific place These “places” need not be directly opposite: Note that the above enzyme is EcoRI, the first restriction endonuclease characterized 5’…GAATTC…3’ 3’…CTTAAG…5’ 5’…G -OH P- AATTC…3’ 3’…CTTAA -P HO- G…5’

19. Sticky Ends

20. Most R.E. Recognition Sequences are Palindromes G^AATT-C C-TTAA^G G^GATC-C C-CTAG^G A^GATC-C T-CTAG^G GC^GGCC-GC CG-CCGG^CG Nodeba Bob Abedon

21. More RE Enzymes EnzymeSequenceProduct EcoRI G^AATTC 5’ sticky ends BamHI G^GATCC 5’ sticky ends Bg1II A^GATCT 5’ sticky ends PvuI CGATC^G 3’ sticky ends PvuII CAG^CTG Blunt end MboI G^ATC 5’ sticky ends HindIII A^AGCTT 5’ sticky ends HinfI G^ANTC 5’ sticky ends Sau3A G^ATC 5’ sticky ends AluI AG^CT Blunt end TaqI T^CGA 5’ sticky ends HaeIII G^GCC 5’ sticky ends NofI GC^GGCCGC 5’ sticky ends

22. Restriction Enzymes are Enzymes That Cut DNA Only at Particular Sequences The enzyme EcoRI cutting DNA at its recognition sequence Different restriction enzymes have different recognition sequences. This makes it possible to create a wide variety of different gene fragments. Restriction enzyme animation

23. Recombinant DNA, Gene Cloning, and Pharmaceutical Production DNA can be cut at specific sequences using restriction enzymes. This creates DNA fragments useful for gene cloning. These are mature and widely utilized biotechnologies.

24. DNA Ligase Upon ligation we now have recombinant DNA

25. Ligation

26. Splicing foreign DNA into a vector  Foreign DNA and plasmid DNA cut with same restriction enzyme  Produces linear molecules with complementary single- stranded ends  Recombinant DNA created by mixing so sticky ends pair  DNA ligase forms covalent bonds, linking the two fragments

27. DNAs Cut by a Restriction Enzyme Can be Joined Together in New Ways These are recombinant DNAs and they often are made of DNAs from different organisms.

28. Plasmids

29. Plasmids are Used to Replicate a Recombinant DNA Plasmids are small circles of DNA found in bacteria. Plasmids replicate independently of the bacterial chromosome. Replication often produces 50-100 copies of a recombinant plasmid in each cell. Pieces of foreign DNA can be added within a plasmid to create a recombinant plasmid.

30. Transformation Note that plasmid is vector that carries DNA into recipient cells via transformation Other vectors include viruses (transduction) as well as otherwise inert projectiles

31. Harnessing the Power of Recombinant DNA Technology – Human Insulin Production by Bacteria

32. http://www.sumanasinc.com/w ebcontent/anisamples/molecula rbiology/plasmidcloning_fla.ht ml animation

33. Human Insulin Production by Bacteria 6) join the plasmid and human fragment and cut with a restriction enzyme

34. Human Insulin Production by Bacteria Mix the recombinant plasmid with bacteria. Screening bacterial cells to learn which contain the human insulin gene is the hard part.

35. Route to the Production by Bacteria of Human Insulin A fermentor used to grow recombinant bacteria. This is the step when gene cloning takes place. The single recombinant plasmid replicates within a cell. Then the single cell with many recombinant plasmids produces trillions of like cells with recombinant plasmid – and the human insulin gene. One cell with the recombinant plasmid

36. Route to the Production by Bacteria of Human Insulin The final steps are to collect the bacteria, break open the cells, and purify the insulin protein expressed from the recombinant human insulin gene.

37. Route to the Production by Bacteria of Human Insulin Overview of gene cloning. Cloning animation

38. Pharming These goats contain the human gene for a clot-dissolving protein that is produced in their milk. Pharming is the production of pharmaceuticals in animals engineered to contain a foreign, drug-producing gene.

39. Genetically Modified Foods Many of our crops in the US are genetically modified. Should they be?

40. GM Crops are Here Today Source: Pew Initiative on Food and Biotechnology, August 2004.

41. Methods for Plant Genetic Engineering are Well-Developed and Similar to Those for Animals

42. Golden Rice is Modified to be Provide a Dietary Source of Vitamin A Worldwide, 7% of children suffer vitamin A deficiency, many of them living in regions in which rice is a staple of the diet. Golden rice (yellow) with standard rice (white).

43. Genetically Modified Crops Genetically Modified Cotton (contains a bacterial gene for pest resistance) Standard Cotton

44. GMOs, Especially Outside the US, Are a Divisive Issue Protesters at the 2000 Montreal World Trade Summit European sentiment

45. Current Concerns by Scientists Focus on Environmental, Not Health, Effects of GM Crops The jury’s still out on the magnitude of GM crop’s ecological impact, but the question is debated seriously.

46. Current Concerns by Scientists Focus on Environmental, Not Health, Effects of GM Crops

47. Genetic probes  Segments of single-stranded DNA that can hybridize to complementary base sequences in target gene  Usually a radioactive piece that “labels” the DNA  Southern blot technique

48. Using a genetic probe to find bacterial cells with a specific recombinant DNA molecule

49. Amplifying DNA in vitro by PCR Small amount of double-stranded DNA DNA precursors Specific nucleic acid primers Taq DNA polymerase  DNA is denatured  Primers attach to primer-binding site on each DNA strand  Each strand acts as template for DNA synthesis

50. Polymerase Chain Reaction Cloning allows the amplification of genotype (DNA) as well as phenotype (proteins) If all you really need is the DNA, then PCR is an easy way to amplify DNA without cloning

51. Amplification of DNA by PCR

52. PCR DNA Amplification

54. Gel Electrophoresis

55. Loading Gel

56. Loaded Gel

57. Run Gel

58. DNA, the Law, and Many Other Applications – The Technology of DNA Fingerprinting A DNA fingerprint used in a murder case. What are we looking at? How was it produced? The defendant stated that the blood on his clothing was his.

59. DNA Fingerprinting Basics Different individuals carry different alleles. Most alleles useful for DNA fingerprinting differ on the basis of the number of repetitive DNA sequences they contain.

60. DNA Fingerprinting Basics If DNA is cut with a restriction enzyme that recognizes sites on either side of the region that varies, DNA fragments of different sizes will be produced. A DNA fingerprint is made by analyzing the sizes of DNA fragments produced from a number of different sites in the genome that vary in length. The more common the length variation at a particular site and the greater the number the sites analyzed, the more informative the fingerprint.

61. A Site With Three Alleles Useful for DNA Fingerprinting DNA fragments of different size will be produced by a restriction enzyme that cuts at the points shown by the arrows.

62. The DNA Fragments Are Separated on the Basis of Size The technique is gel electrophoresis. The pattern of DNA bands is compared between each sample loaded on the gel. Gel electrophoresis animation

63. Possible Patterns for a Single “Gene” With Three Alleles In a standard DNA fingerprint, about a dozen sites are analyzed, with each site having many possible alleles.

64. A DNA Fingerprint When many genes are analyzed, each with many different alleles, the chance that two patterns match by coincidence is vanishingly small. DNA detective animation HGP fingerprinting page

65. DNA and the Law SLT 3/8/05 Some applications of DNA fingerprinting in the justice system.

66. 2-D Protein Electrophoresis

67. DNA typing

68. Southern Blotting

69. Northern Blot A Northern Blot is the same as a Southern Blot-except instead of probing for DNA- the prob is for RNA Used to detect whether or not transcription is occuring

70. Western Blot Same as Southern/Northern except the probe is for protein Used to detect whether a particular gene is being “turned on” or “off”

71. DNA sequencing  Based on chain termination method  Yields information about Structure of gene Probable amino acid sequences of its encoded proteins

72. Chain termination method of DNA sequencing

73. DNA Sequencing

76. DNA Sequencer

77. Shotgun Sequencing

78. Transgenic organisms  Foreign DNA incorporated into their genetic material  Gene target Single gene inactivated or “knocked out” “Knockout mice” used in studying genes  Mutagenesis screening Male mice treated with mutagens and studied

79. A transgenic mouse Mouse on right is normal; mouse on left is transgenic animal expressing rat growth hormone

80. Transgenic rice “Golden rice” shown intermixed with white rice contain high concentrations of beta-carotene

81. Safety guidelines  Safety concerns Introduction of transgenic organisms into the environment Health effects on humans from consuming GM crops  Safety measures Special facilities designed to hold pathogenic organisms Science of risk assessment

82. Gene Therapy One example of this might be done… is essentially cloning into animals

83. Injecting DNA into Egg

84. Genome Comparisons

85. The Stem Cell Concept A stem cell is an undifferentiated, dividing cell that gives rise to a daughter cell like itself and a daughter cell that becomes a specialized cell type.

86. Stem Cells are Found in the Adult, but the Most Promising Types of Stem Cells for Therapy are Embryonic Stem Cells

87. The Inner Cell Mass is the Source of Embryonic Stem Cells The embryo is destroyed by separating it into individual cells for the collection of ICM cells.

88. Some Thorny Ethical Questions Is it ethical to harvest embryonic stem cells from the “extra” embryos created during in vitro fertilization? Are these masses of cells a human?

89. The Promise and Possible Perils of Stem Cells

90. Additional Potential Dilemmas – Therapeutic Cloning to Obtain Matched Embryonic Stem Cells Cells from any source other than you or an identical twin present the problem of rejection. If so, how can matched embryonic stem cells be obtained? A cloned embryo of a person can be made, and embryonic stem cells harvested from these clones. Cultured mouse embryonic stem cells.

91. Therapeutic Cloning Is there any ethical difference between therapeutic and reproductive cloning?

92. HIV/Pregnancy Tests Done using body’s own immune response ELISA test Cells naturally have antigens on their outer surface. The antibodies respond to the antigens in an immune response Antibodies and antigens fit together “like a glove”

95. http://www.elispot- analyzers.de/english/elisa- animation.html Animation

96. http://www.genome.gov/Pages /EducationKit/download.html DNA technology video

97. Online Tools Buying primers (custom oligos): http://www.qiagen.com/http://www.qiagen.com/ 2x2 sequence comparisons: http://www2.igh.cnrs.fr/bin/align- guess.cgihttp://www2.igh.cnrs.fr/bin/align- guess.cgi n x n sequence comparisons: http://www.genebee.msu.su/services/malign_reduced.html http://www.genebee.msu.su/services/malign_reduced.html Sequence manipulation: http://arbl.cvmbs.colostate.edu/molkit/manip/index.html http://arbl.cvmbs.colostate.edu/molkit/manip/index.html Sequence translation: http://arbl.cvmbs.colostate.edu/molkit/translate/index.html http://arbl.cvmbs.colostate.edu/molkit/translate/index.html Restriction Enzymes: http://rebase.neb.com/rebase/rebase.htmlhttp://rebase.neb.com/rebase/rebase.html Restriction sites: http://www.ccsi.com/firstmarket/cutter/cut2.htmlhttp://www.ccsi.com/firstmarket/cutter/cut2.html Sequence searches: http://www.ncbi.nlm.nih.gov/blast/http://www.ncbi.nlm.nih.gov/blast/ Other tools: http://molbiol-tools.ca/http://molbiol-tools.ca/