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GENETIC MODIFICATIONS and BIOTECHNOLOGY. Genetic engineering: altering the sequence of DNA Ideas established in early 70's by 2 American researchers, Stanley Cohen (worked with plasmids) and Herbert Boyer (restriction endonucleases) - PowerPoint PPT Presentation
GENETIC MODIFICATIONS and BIOTECHNOLOGY Genetic engineering: altering the sequence of DNA Ideas established in early 70's by 2 American researchers, Stanley Cohen (worked with plasmids) and Herbert Boyer (restriction endonucleases) Initially had no commercial applications for their experiments, but things changed quickly. In 1976 Boyer cofounded Genetech, first biotech company to go public on the stock market.
1978: somatostatin became the first human hormone produced by this technology.Techniques are now commonplace in molecular biology labs worldwide.Other examples:Insulin, 90%+ diabetics are reliant on human insulin supplied by bacteria.Somatropin, used to treat human growth deficiency, from dwarfism, Turner's syndrome, also used for AIDS-associated wasting syndrome now
BIOTECHNOLOGY Biotechnology involves the manipulation of DNA and protein synthesis. Molecular biologists analyze and alter genes and their respective proteins Examples:Genetic screening: scanning for genetic mutationsGene therapy: the alteration of a genetic sequence in an organism to prevent or treat a genetic disorder by creating working proteins.Transgenic plants: inserting genes to provide new proteins, giving plants new propertiesDNA fingerprinting: analyzing pattern of bands that are unique to an individual.Human Genome Project...
The tools the scientists use are very specific to DNA and its environment.The DNA first has to be cut out of the source organismThe DNA has to be isolatedDNA can then be introduced into the host DNARecombinant DNA is DNA from one source organism being put into the DNA of a host organism.
1) Cutting Out DNA: RESTRICTION ENDONUCLEASES / ENZYMES are naturally occurring enzymes that act like a pair of molecular scissors to cut DNA in a predictable and precise manner, at a specific nucleotide sequence called a recognition site .Hamilton Smith, John Hopkins University, won the Nobel Prize in 1978 for discovering restriction enzymes in bacteria (Hind III). He found their main purpose was to cut foreign DNA that tried to invade a bacterial cell (i.e. DNA from a virus).Restriction enzymes are named according to the bacteria from which they originate.Bam HI is from Bacillus amyloliquefaciens, strain H. The I indicates it was the first endonuclease isolated from that strain.
Recognition sites are usually:4 8 base pairs in length. Palindromic: both strands have the same sequence when read in the 5' to 3' direction.Table 1 p 279: examples
The restriction enzyme EcoRI binds to 5'-GAATTC-3' / 3'-CTTAAG-5'
EcoRI finds this recognition site and breaks the phosphodiester bond between G and A, then it pulls apart the two strands by breaking the H-bonds between the complementary base pairs.Produces what are called sticky ends (unpaired nucleotides at each end).
Other restriction enzymes like AluI produce blunt ends, or ends with no overhang.Sticky ends are usually more helpful to molecular biologists as they can easily be joined with other DNA fragments cut by the same restriction enzyme. Blunt ends are harder to fuse to a foreign DNA molecule.
A host must protect its own DNA from endonucleases.Methylases are enzymes that place a methyl group (CH3) on recognition sites which prevents the restriction enzyme from cleaving the DNA at that spot.Host DNA is methylated, but foreign DNA is not, so it is can be cut by the host cell's restriction enzymes.
2) ISOLATING DNA FRAGMENTS: GEL ELECTROPHORESISRestriction endonucleases cleave the DNA into smaller fragmentsGel electrophoresis is used to isolate the required gene segment from the rest of the DNAThe fragments of DNA will be run through a porous agarose gel using electricity.The fragments of DNA are pulled through pores in the gel due to their negative charge.Smaller fragments will move faster than larger because they can fit through the pores better.
VIEWING THE GELhttp://www.mcps.k12.md.us/departments/intern/stp/images/gel_electrophorsis.jpghttp://www.life.uiuc.edu/molbio/geldigest/fullsize/geldraw.jpg
3) INTRODUCING FOREIGN DNA INTO A HOST: PLASMIDS and TRANSFORMATIONhttp://www.rpgroup.caltech.edu/courses/PBL/images_dnascience/pZ%20Plasmid.gifPlasmids are used by biologists to incorporate genes they want replicated or transcribed/translated in vast amounts in little time into bacterial cells.Vector: vehicle used to introduce DNA into a host cell, ie a plasmid or virus.
STEPS:http://employees.csbsju.edu/hjakubowski/classes/ch331/dna/plasmid.gif1. Restriction enzymes are used to cut out the gene from the original cell AND to open the bacterial plasmid.2. Once the foreign gene is isolated it can then be inserted into the plasmid. The plasmid is now considered recombinant DNA.
TRANSFORMATION3. The recombinant DNA is then introduced into a bacterial cell. Sometimes a host cell must be manipulated to take up the foreign DNA plasmid.Transformation: introduction of foreign DNA (usually by plasmid or virus) into a bacterial cell.Host cell: cell that has taken up foreign plasmid or virus and whose cellular machinery is being used to express the foreign DNA.Competent cell: cell that readily takes up foreign DNA.
4) Selection and CloningGeneration of DNA fragments using restriction endonucleasesConstruction of a recombinant DNA moleculeIntroduction into a host cellSelectionCells that have been successfully transformed must be isolated (usually by antibiotic resistance)The vectors used for cloning usually carry an antibiotic-resistance gene. Growth of colonies on media containing the antibiotic indicates successful transformation.Colonies are isolated from media and grown in culture to produce multiple copies (clones) of the recombinant DNAWhen the bacteria replicates the recombinant DNA plasmid, the new gene product will be formed multiple times (ie. the gene is cloned).
PCR another means of copying DNA in large numbersstands for Polymerase Chain Reaction, developed in the late 1980's by Kary Mullis; awarded Nobel Prize in Chemistry in 1992.Does not require a plasmid. Therefore when the process is finished, it is not necessary to remove the plasmid from the bacteria and the desired gene from the plasmid. The fragment is copied directly.Useful for forensic criminal investigations, medical diagnosis, genetic research. Only small amounts of DNA are needed.
PCR ProcessPCR is amplification of a DNA sequence by repeated cycles of strand separation and replication in the laboratory (DNA photocopying).
After about 30 cycles more than 1 billion copies of the targeted area will exist (230).1. Strands are separated using heat2. DNA primers, synthesized in the lab, are created to complement the start of the target area to be copied.3. Temp is decreased and the primers anneal4. Taq polymerase (from bacteria) creates new strands of target area5. Sequence is repeated over and over on each of the new strands builthttp://users.ugent.be/~avierstr/principles/pcrcopies.gif
RFLPRestriction fragment length polymorphismEntire genome is subjected to restriction enzyme digestionDNA run on an agarose gel, using gel electrophoresisSingle stranded DNA transferred to a membranessDNA hybridized with radioactive probes for specific regions (such as alleles or areas known as variable number tandem repeats, that lead to a specific disease).An X-ray film is developed, called an autoradiogram, and the pattern can then be used to identify a suspect, or detect a genetic mutation.http://homepage.smc.edu/HGP/images/rflp.gif
SEQUENCING DNASanger dideoxy method: uses DNA replication and dideoxy nucleoside triphosphates to determine the complementary strand.Developed by Frederick Sanger and colleagues at Cambridge University in Great Britain in 1977. They used it to sequence the genome of a bacteriophage (viral DNA) 5386 base pairs long.
- Dideoxy nucleosides are missing the -OH group on carbon 3 and therefore inhibit the process of replication.- Everytime one is added, the process stops and only small sequences are created. - These sequences can be run on a gel, and since they will run from shortest to longest, you can actually read the sequence by knowing which dideoxy nucleoside was used and therefore stopped replication at each point.
Sanger dideoxy method
Fluorescent Detection of OligonucleotidesThe Human Genome Project used a similar method, but also included fluorescence on each dideoxy nucleoside, so the A, G, T and C's lit up as different colours. A computer read the sequence from gel electrophoresis. Thousands of sequencers worked 24 hours a day, 7 days a week to decipher 3 billion base pairs.
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