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DNA Technology

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make multiple copies of a particular gene for use in basic research or insertion ... using nucleic acid hybridization (this technique is called Southern blotting) ... – PowerPoint PPT presentation

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Title: DNA Technology


1
DNA Technology Genomics
  • CHAPTER 20

2
DNA Cloning (gene cloning)
  • methods
  • insert gene of interest into a bacterial plasmid
    allow the recombinant bacterium to reproduce
  • PCR (polymerase chain reaction)
  • uses
  • make multiple copies of a particular gene for
    use in basic research or insertion into another
    organisms genome
  • harvest large quantities of the encoded protein
    from bacterial cultures carrying the cloned gene

3
Restriction Enzymes
  • enzymes that cut DNA at specific locations
    (restriction sites) yielding restriction
    fragments
  • used to insert genes into bacterial plasmids
  • the sticky ends of the restriction fragments can
    base-pair with the sticky ends of a cut plasmid
    then be sealed together by DNA ligase

4
Genomic Libraries
  • the process of DNA cloning usually results in
    thousands of different types of recombinant
    plasmids
  • the complete set of these recombinant plasmids is
    called a genomic library
  • one method for identifying bacteria with the
    recombinant plasmid containing the gene of
    interest is nucleic acid probe hybridization

white colonies
5
Nucleic Acid Hybridization
6
Expressing Eukaryotic Genes in Prokaryotic Cells
  • Problem 1 bacterial cell doesnt recognize the
    eukaryotic genes promoter
  • solution link the gene of interest to a highly
    active prokaryotic promoter that the bacterial
    cell will recognize
  • this is accomplished by inserting the gene of
    interest into a cloning vector (plasmid) that
    contains a this promoter
  • Problem 2 eukaryotic genes contain introns
    bacterial cells lack RNA-splicing machinery
  • solution insert the cDNA (complimentary DNA)
    form of the gene

7
Creating cDNA
  • mRNA transcript of gene of interest is combined
    with reverse transcriptase to create a
    complimentary DNA strand
  • the mRNA strand is then degraded and the
    complimentary, second strand of DNA is created by
    adding DNA polymerase
  • the resulting cDNA molecule is modified by adding
    sticky ends so that it can be inserted into a
    cloning vector

8
Eukaryotic Hosts for DNA Cloning
  • yeast cells (which also contain plasmids) can be
    used as hosts for DNA cloning to avoid
    eukaryotic-prokaryotic incompatibility

9
PCR (Polymerase Chain Reaction)
  • alternative method for cloning a gene
  • used primarily when the source of DNA is scanty
    or impure
  • applications
  • amplify fragments of ancient DNA
  • amplify DNA from fingerprints or tiny amounts of
    blood, tissue, or semen found at crime scenes
  • amplify DNA from embryonic cells to test for
    genetic disorders

10
Restriction Fragment Analysis
  • the DNA fragments produced by restriction enzyme
    digestion can be sorted by gel electrophoresis
  • uses a gel an electric field to separate
    nucleic acids or proteins on the basis of size
    and charge
  • the bands produced by gel electrophoresis can be
    analyzed for a particular gene using nucleic acid
    hybridization (this technique is called Southern
    blotting)

11
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12
Genome Mapping
  • 3 stages
  • linkage mapping
  • physical mapping
  • DNA sequencing

13
Cytogenetic Maps
  • the starting point for DNA mapping
  • shows a chromosomes banding pattern and the
    location of specific genes on the chromosome
  • the genes were located using a technique called
    FISH (fluorescence in situ hybridization) in
    which fluorescently labeled probes are allowed to
    hybridize to an immobilized array of whole
    chromosomes

14
Linkage Maps
  • a map of genetic markers based on recombination
    frequencies
  • the markers can be
  • genes
  • RFLPs (restriction fragment length polymorphisms)
    different restriction fragment patterns on
    homologous chromosomes due to differences in
    their restriction sites
  • simple sequence DNA sections of DNA that
    contain repeated short sequences

15
Physical Maps
  • express the distance (number of base-pairs)
    between markers
  • made by cutting the DNA of a chromosome into a
    number of restriction fragments and then
    determining the original order of the fragments
    in the chromosome by looking for areas where the
    fragments overlap

16
DNA Sequencing
  • determining the complete nucleotide sequence of
    each chromosome
  • techniques for DNA sequencing include
  • dideoxy chain-termination method
  • shotgun approach developed by Celera Genomics
  • skips the linkage physical mapping stages
  • takes random DNA fragments uses computer
    programs to sequence and order them

17
shotgun approach
dideoxy chain- termination method
18
Human Genome Project
  • sequencing of the 22 autosomes and the sex
    chromosomes (largely completed in 2003)
  • also involves mapping the genomes of other
    species important to biological research
  • allows scientists to study whole sets of genes
    their interactions

19
Searching for Protein-Coding Genes
  • scientists used software to scan DNA sequences
    for
  • transcriptional translational start and stop
    sequences
  • RNA-splicing sites
  • short coding sequences (expressed sequence tags)
    similar to those in known genes

20
Determining Gene Function
  • disable gene and observe the consequences
  • in vitro mutagenesis a mutation is introduced
    in a cloned gene then returned to the cell
  • RNA interference (RNAi) synthetic,
    double-stranded RNA molecules matching the
    sequence of a particular gene are used to trigger
    the breakdown or block the translation of the
    genes mRNA

21
Studying Gene Expression
  • to determine which genes are expressed in a
    particular cell, scientists can use DNA
    microarray assays
  • isolate all the mRNAs made in a particular cell
  • use them to make fluorescently-labeled cDNAs by
    reverse transcription
  • apply the cDNA to a microarray containing all
    the organisms genes

22
Comparing Genomes of Different Species
  • allows scientists to determine evolutionary
    relationships between species
  • helps scientists better understand the human
    genome
  • provides scientists with a scaffold for
    organizing the DNA sequences of closely related
    species
  • makes it easier for scientists to correlate
    phenotypic differences between species with
    particular genetic differences
  • can be used to help study certain genetic diseases

23
Future Areas of Research
  • Proteomics studying the full protein sets
    encoded by genomes
  • studying human evolution the history of human
    populations through the identification of SNP
    sites
  • SNPs (single nucleotide polymorphisms) are single
    base-pair variations that account for the genetic
    differences between individuals (which is only
    about 0.1)

24
Applications of DNA Technology
  • Medicine
  • Pharmaceuticals
  • Forensics
  • Environmental Cleanup
  • Agriculture

25
Medical Applications
  • diagnosing diseases
  • detecting susceptibility of diseases
  • treating diseases
  • gene therapy alteration of an afflicted
    individuals genes

26
Pharmaceutical Applications
  • manufacture large quantities of human proteins
    (ex insulin)
  • production of vaccines
  • pharmacogenomics

27
Forensic Applications
  • DNA fingerprinting

28
Environmental Cleanup
  • genetically engineered microbes are being used or
    created to
  • remove heavy metals from the environment
  • cleanup highly toxic mining wastes
  • degrade chlorinated hydrocarbons in wastewater
  • breakdown chemical released during oil spills
  • breakdown toxic wastes in waste dumps

29
Agricultural Applications
  • make vaccines growth hormones for treating farm
    animals
  • creating transgenic animals plants
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