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Genetic Technologies

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Genetic Technologies By: Ting-Yu Tsai Han Keyl Kim 19.1 Patenting DNA Biotechnology -Use or alteration of cells or biological molecules for specific applications. – PowerPoint PPT presentation

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Title: Genetic Technologies


1
Genetic Technologies
  • By Ting-Yu Tsai
  • Han Keyl Kim

2
19.1 Patenting DNA
  • Biotechnology
  • -Use or alteration of cells or biological
    molecules for specific applications.
  • Organisms that harbor DNA from other species are
    termed Transgenic and their DNA is called
    recombinant DNA

3
The OncoMouse or Harvard mouse is a type of
laboratory mouse that has been genetically
modified using modifications designed by Philip
Leder and Timothy A. Stewart of Harvard
University to carry a specific gene called an
activated oncogene. The activated oncogene
significantly increases the mouses
susceptibility to cancer, and thus makes the
mouse suitable for cancer research. The rights to
the invention are owned by DuPont. OncoMouse(R)
is a registered trademark.
Patented OncoMouse
The Laboratory, or The Passion of OncoMouse
4
Key Concept
  • Biotechnology is the use of modification of cells
    or biological molecules for a specific
    application.
  • Patent law regarding DNA has evolved with the
    technology since the 1970s, and is still changing.

5
19.2 Amplifying DNA PCR
  • Polymerase Chain Reaction (PCR) are the
    technologies for amplified DNA that invented by
    Kary Mullis in 1983. He then won the Nobel prize
    for PCR in 1993.
  • Use of PCR
  • - DNA cloning for sequencing
  • - DNA-based phylogeny
  • - Diagnosis of hereditary diseases
  • - Functional analysis of genes
  • - Identification of genetic fingerprints
  • - Detection and diagnosis of infectious
    diseases

6
PCR STEPS
  • Initialization Heating the reaction to 94-96C.
    Its only required for DNA polymerases.
  • Denaturation First regular cycling. Heat for
    separate 2 strands of the target DNA.
  • Annealing 2 short primers and Taq1 DNA
    polymerase added. Cool to allow primers form
    hydrogen bond with ends of target sequence.
  • Extension DNA polymerase adds nucleotides to the
    3 end of each primer.
  • Final elongation This step is to ensure that
    any remaining single-stranded DNA is fully
    extended.
  • Final hold May be employed for short-term
    storage of the reaction.

7
19.3 Modifying DNA
  • Modifying DNA
  • -Researchers thought about uses and risks of
    mixing DNA from different species.
  • -Recombinant DNA technology was safer than
    expected, and the technology has spread to
    industry more swiftly and in more diverse ways.

8
Cloning vectors
  • Plasmid
  • Bacteriophage
  • Bacterial artificial
  • Chromosome (BAC)
  • Yeast artificial
  • Chromosome (YAC)

Size of insert accepted up to 15
Size of insert accepted up to 90
Size of insert accepted 100 to 500
Size of insert accepted up to 15
9
  • Genomic library a population of host bacteria,
    each of which carries a DNA molecule that was
    inserted into a cloning vector, such that the
    collection of cloned DNA molecules represents the
    entire genome of the source organism. This term
    also represents the collection of all of the
    vector molecules, each carrying a piece of the
    chromosomal DNA of the organism, prior to the
    insertion of these molecules into the host cells.
  • DNA probe a single-stranded DNA molecule used in
    laboratory experiments to detect the presence of
    a complementary sequence among a mixture of other
    singled-stranded DNA molecules.
  • cDNA library is a collection of cloned cDNA
    (complementary DNA) fragments inserted into a
    collection of host cells, which together
    constitute some portion of the transcriptome of
    the organism. cDNA is produced from fully
    transcribed mRNA found in the nucleus and
    therefore contains only the expressed genes of an
    organism. Similarly, tissue specific cDNA
    libraries can be produced. In eukaryotic cells
    the mature mRNA is already spliced, hence the
    cDNA produced lacks introns and can be readily
    expressed in a bacterial cell. While information
    in cDNA libraries is a powerful and useful tool
    since gene products are easily identified, the
    libraries lack information about enhancers,
    introns, and other regulatory elements found in a
    genomic DNA library.

10
Transgenic Plants
  • Transgenic plants are easier to create than
    transgenic animals because plants can be derived
    from somatic cells.
  • Protoplasts The denude plant cells had their
    cell walls removed by some manipulations.
  • Protoplasts

11
Ti Plasmid
  • Ti plasmid is a circular plasmid that is a part
    of the genetic equipments that Agrobacterium
    tumefaciens use to transduce its genetic material
    to plants. It normally causes a tumor-like
    growth.
  • Producing a transgenic plant

12
Bacillus Thuringiensis
  • Bt is a soil-dwelling bacterium that commonly
    used as a pesticide.
  • When bt gene is bring into corn cells via a Ti
    plasmid, the cells regenerate corn plants and
    produce their own insecticide.
  • Possible problems The pollen form Bt maize could
    kill the monarch butterfly.

13
References
  • http//en.wikipedia.org/wiki/Polymerase_chain_reac
    tion
  • Chapter 19 Genetic Technologies, Human Genetics
    8th Edition, McGraw-Hill Companies, Ricki Lewis,
    2008.
  • http//www.everythingbio.com/
  • http//scienceblogs.com/insolence/2007/06/the_auti
    sm_omnibus_the_difference_betwee.php
  • http//www.biology.lsu.edu/webfac/nkato/methods/me
    thodImages/Protoplast.jpg
  • http//www.mun.ca/biology/desmid/brian/BIOL2060/BI
    OL2060-20/2032.jpg
  • http//en.wikipedia.org/wiki/Bacillus_thuringiensi
    s
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