1. Biotechnology Chapter 17

2. 2 DNA Manipulation The molecular biology revolution started with the discovery of restriction endonucleases -Enzymes that cleave DNA at specific sites These enzymes are significant in two ways 1. Allow a form of physical mapping that was previously impossible 2. Allow the creation of recombinant DNA molecules (from two different sources)

3. 3 DNA Manipulation Restriction enzymes recognize DNA sequences termed restriction sites There are two types of restriction enzymes: -Type I = Cut near the restriction site -Rarely used in DNA manipulation -Type II = Cut at the restriction site -The sites are palindromes -Both strands have same sequence when read 5 ’ to 3 ’

4. 4 DNA Manipulation Type II enzymes produce staggered cuts that generate “sticky ends” -Overhanging complementary ends Therefore, fragments cut by the same enzyme can be paired DNA ligase can join the two fragments forming a stable DNA molecule

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6. 6 Gel Electrophoresis A technique used to separate DNA fragments by size The gel (agarose or polyacrylamide) is subjected to an electrical field The DNA, which is negatively-charged, migrates towards the positive pole -The larger the DNA fragment, the slower it will move through the gel matrix DNA is visualized using fluorescent dyes

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9. 9 Transformation Transformation is the introduction of DNA from an outside source into a cell Natural transformation occurs in many species -However, not in E. coli, which is used routinely in molecular biology labs -Artificial transformation techniques have been developed to introduce foreign DNA into it

10. 10 Molecular Cloning A clone refers to a genetically identical copy Molecular cloning is the isolation of a specific DNA sequence (usually protein-encoding) -Sometimes called gene cloning The most flexible and common host for cloning is E. coli Propagation of DNA in a host cell requires a vector

11. 11 Vectors Plasmids are small, circular extrachromosomal DNA molecules -Used for cloning small pieces of DNA -Have three important components 1. Origin of replication 2. Selectable marker 3. Multiple cloning site (MCS)

12. 12 Vectors

13. 13 Vectors Phage vectors are modified bacterial viruses -Most based on phage lambda ( ) of E. coli -Used to clone inserts up to 40 Kbp -Have two features not shared with plasmid vectors -They kill their host cells -They have linear genomes -Middle replaced with inserted DNA

14. 14 Vectors

15. 15 Vectors Artificial chromosomes -Used to clone very large DNA fragments -Bacterial artificial chromosomes (BACs) -Yeast artificial chromosomes (YACs)

16. 16 DNA Libraries A collection of DNA fragments from a specific source that has been inserted into host cells A genomic library represents the entire genome A cDNA library represents only the expressed part of the genome -Complementary DNA (cDNA) is synthesized from isolated mRNA using the enzyme reverse transcriptase

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20. 20 DNA Libraries Molecular hybridization is a technique used to identify specific DNAs in complex mixtures -A known single-stranded DNA or RNA is labeled -It is then used as a probe to identify its complement via specific base-pairing -Also termed annealing

21. 21 DNA Libraries Molecular hybridization is the most common way of identifying a clone in a DNA library -This process involves three steps: 1. Plating the library 2. Replicating the library 3. Screening the library

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23. 23 DNA Analysis Restriction maps -Molecular biologists need maps to analyze and compare cloned DNAs -The first maps were restriction maps -Initially, they were created by enzyme digestion & analysis of resulting patterns -Many are now generated by computer searches for cleavage sites

24. 24 DNA Analysis Southern blotting -A sample DNA is digested by restriction enzymes & separated by gel electrophoresis -Gel is transferred (“blotted”) onto a nitrocellulose filter -Then hybridized with a cloned, radioactively-labeled DNA probe -Complementary sequences are revealed by autoradiography

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28. 28 DNA Analysis Northern blotting -mRNA is electrophoresed and then blotted onto the filter Western blotting -Proteins are electrophoresed and then blotted onto the filter -Detection requires an antibody that can bind to one protein

29. 29 DNA Analysis RFLP analysis -Restriction fragment length polymorphisms (RFLPs) are generated by point mutations or sequence duplications -These fragments are often not identical in different individuals -Can be detected by Southern blotting

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31. 31 DNA Analysis DNA fingerprinting -An identification technique used to detect differences in the DNA of individuals -Makes use of a variety of molecular procedures, including RFLP analysis -First used in a US criminal trial in 1987 -Tommie Lee Andrews was found guilty of rape

32. 32 DNA Analysis

33. 33 DNA Analysis DNA sequencing -A set of nested fragments is generated -End with known base -Separated by high- resolution gel electrophoresis, resulting in a “ladder” -Sequence is read from the bottom up

34. 34 DNA Analysis DNA sequencing -The enzymatic method was developed by Frederick Sanger -Dideoxynucleotides are used as chain terminators in DNA synthesis reactions

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36. 36 DNA Analysis DNA sequencing -The enzymatic technique is powerful but is labor intensive and time-consuming -The development of automated techniques made sequencing faster and more practical -Fluorescent dyes are used instead of radioactive labels -Reaction is done in one tube -Data are assembled by a computer

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38. 38 DNA Analysis Polymerase chain reaction (PCR) -Developed by Kary Mullis -Allows the amplification of a small DNA fragment using primers that flank the region -Each PCR cycle involves three steps: 1. Denaturation (high temperature) 2. Annealing of primers (low temperature) 3. DNA synthesis (intermediate temperature) -Taq polymerase

39. 39 After 20 cycles, a single fragment produces over one million (2 20 ) copies!

40. 40 After 20 cycles, a single fragment produces over one million (2 20 ) copies! (Cont.)

41. 41 DNA Analysis Polymerase chain reaction (PCR) -Has revolutionized science and medicine because it allows the investigation of minute samples of DNA -Forensics -Detection of genetic defects in embryos -Analysis of mitochondrial DNA from early human species

42. 42 DNA Analysis Yeast two-hybrid system -Used to study protein-protein interactions -Gal4 is a transcriptional activator with a modular structure -The Gal4 gene is split into two vectors -Baitvector: has DNA-binding domain -Prey vector: has transcription-activating domain -Neither of these alone can activate transcription

43. 43 DNA Analysis Yeast two-hybrid system -When other genes are inserted into these vectors, they produce fusion proteins -Contain part of Gal4 and the protein of interest -If the proteins being tested interact, Gal4 function will be restored -A reporter gene will be expressed -Detected by an enzyme assay

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46. 46 Genetic Engineering Has generated excitement and controversy Expression vectors contain the sequences necessary to express inserted DNA in a specific cell type Transgenic animals contain genes that have been inserted without the use of conventional breeding

47. 47 Genetic Engineering In vitro mutagenesis -Ability to create mutations at any site in a cloned gene -Has been used to produce knockout mice, in which a known gene is inactivated -The effect of loss of this function is then assessed on the entire organism -An example of reverse genetics

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51. 51 Medical Applications Human proteins -Medically important proteins can be produced in bacteria -Human insulin -Interferon -Atrial peptides -Tissue plasminogen activator -Human growth hormone

52. 52 Medical Applications

53. 53 Medical Applications Vaccines -Subunit vaccines: Genes encoding a part of the protein coat are spliced into a fragment of the vaccinia (cowpox) genome -DNA vaccines: Depend on the cellular immune response (not antibodies)

54. 54 Medical Applications

55. 55 Medical Applications Gene therapy -Adding a functional copy of a gene to correct a hereditary disorder -Severe combined immunodeficiency disease (SCID) illustrates both the potential and the problems -Successful at first, but then patients developed a rare leukemia

56. 56 Agricultural Applications Ti (tumor-inducing) plasmid is the most used vector for plant genetic engineering -Obtained from Agrobacterium tumefaciens, which normally infects broadleaf plants -However, bacterium does not infect cereals such as corn, rice and wheat

57. 57 Agricultural Applications

58. 58 Agricultural Applications

59. 59 Agricultural Applications Gene guns -Uses bombardment with tiny gold particles coated with DNA -Possible for any species -However, the copy number of inserted genes cannot be controlled

60. 60 Agricultural Applications Herbicide resistance -Broadleaf plants have been engineered to be resistant to the herbicide glyphosate -This allows for no-till planting

61. 61 Agricultural Applications Pest resistance -Insecticidal proteins have been transferred into crop plants to make them pest-resistant -Bt toxin from Bacillus thuringiensis Golden rice -Rice that has been genetically modified to produce  -carotene (provitamin A) -Converted in the body to vitamin A

62. 62 Agricultural Applications

63. 63 Agricultural Applications Adoption of genetically modified (GM) crops has been resisted in some areas because of questions about: -Crop safety for human consumption -Movement of genes into wild relatives -Loss of biodiversity

64. 64 Agricultural Applications Biopharming -Transgenic plants are used to produce pharmaceuticals -Human serum albumin -Recombinant subunit vaccines -Against Norwalk and rabies viruses -Recombinant monoclonal antibodies -Against tooth decay-causing bacteria

65. 65 Agricultural Applications Transgenic animal technology has not been as successful as that in plants -One interesting example is the EnviroPig -Engineered to carry the gene for the enzyme phytase -Breaks down phosphorus in feed -Reduces excretion of harmful phosphates in the environment

66. 66 Agricultural Applications