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12-02-09 Notes

Insulin (cont’d)
The insulin production problem:
       -create a gene without introns, do not need to process mRNA
               -c-DNA

Making c-DNA
      -If a cell is making a protein there will be mRNAs for that protein
      in the cytoplasm
      -introns removed, DNA moves out into ribosomes where it is
      replicated
      -use mRNA to make a DNA copy of the mRNA strand
      -Extract the mRNA and make a DNA copy with reverse
      transcriptase.
      -retroviruses carry information as RNA

       -Reverse transcriptase is an enzyme found in retroviruses like HIV—viral
       RNA enters host cell
       -complimentary base pairs with RNA, creates DNA
       -then the new single strand of DNA is used as a template to make the
       other side of the DNA molecule
       -No introns present, introns locked up in ribosomes using c-DNA
       -most

Agricultural uses of DNA technology
       -Due to cell wall, plant cells are easily separated
       -single cell can grow
       -in right environment [temperature, hormones, etc]
       -divide by mitosis, create new plant
       -totipotency – in plants, not animals

       Ti (tumour inducing) Plasmid Vector
              -Agrobacterium tumefacies
                     --causes gnarles on sides of tree bases, protecting
                     internal bacteria

DNA Technology Methods
     -Gel Electrophoresis
     -PCR – Polymerase Chain Reaction
     -Restriction Fragment Length Polymprphisms (RFLP’s)
     -DNA Sequencing

RFLP Analysis (Restriction Fragment Length Polymorphisms)
     -mutation in restriction site
     -2nd person’s DNA = different.
Gel Electrophoresis
      -Wells in the gel are filled with DNA samples which were cut into
      fragments by a restriction enzyme
      -Electric current goes through gel, fragments of DNA attracted to
      positive end of gel, repelled from negative end, attracted to
      positive end.
      -Short pieces move through gel rapidly, long ones move slowly
             -larger length, slower transport

DNA Fingerprint
     -Comparison of restriction fragments that are made from DNA
     fragments separated by restriction enzymes

PCR Polymerase Chain Reaction
     -Copies of small DNA samples can be made.
     -Make many copies of small amount of DNA so there is enough
     to work with

Practical Applications of DNA Technology
       -Diagnosis of Diseases
       -Human Gene Therapy
       -Pharmaceutical Products
       -Forensic Uses of DNA Technology
       -Environmental Uses of DNA Technology
       -Agricultural Uses of DNA Technology

Chapter 24 – page 485

The Immune System

Nonspecific Defences
     Skin
     -Skin glands secrete enzymes
     Mucus membranes
     -Digestive system – acids, enzymes
     -Respiratory system – cilia

      Phagocytes
      -White blood cells – phagocytic, engulf bacteria and dead cells
            -Neutrophils
            -Monocytes

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12 02 09 Notes

  • 1. 12-02-09 Notes Insulin (cont’d) The insulin production problem: -create a gene without introns, do not need to process mRNA -c-DNA Making c-DNA -If a cell is making a protein there will be mRNAs for that protein in the cytoplasm -introns removed, DNA moves out into ribosomes where it is replicated -use mRNA to make a DNA copy of the mRNA strand -Extract the mRNA and make a DNA copy with reverse transcriptase. -retroviruses carry information as RNA -Reverse transcriptase is an enzyme found in retroviruses like HIV—viral RNA enters host cell -complimentary base pairs with RNA, creates DNA -then the new single strand of DNA is used as a template to make the other side of the DNA molecule -No introns present, introns locked up in ribosomes using c-DNA -most Agricultural uses of DNA technology -Due to cell wall, plant cells are easily separated -single cell can grow -in right environment [temperature, hormones, etc] -divide by mitosis, create new plant -totipotency – in plants, not animals Ti (tumour inducing) Plasmid Vector -Agrobacterium tumefacies --causes gnarles on sides of tree bases, protecting internal bacteria DNA Technology Methods -Gel Electrophoresis -PCR – Polymerase Chain Reaction -Restriction Fragment Length Polymprphisms (RFLP’s) -DNA Sequencing RFLP Analysis (Restriction Fragment Length Polymorphisms) -mutation in restriction site -2nd person’s DNA = different.
  • 2. Gel Electrophoresis -Wells in the gel are filled with DNA samples which were cut into fragments by a restriction enzyme -Electric current goes through gel, fragments of DNA attracted to positive end of gel, repelled from negative end, attracted to positive end. -Short pieces move through gel rapidly, long ones move slowly -larger length, slower transport DNA Fingerprint -Comparison of restriction fragments that are made from DNA fragments separated by restriction enzymes PCR Polymerase Chain Reaction -Copies of small DNA samples can be made. -Make many copies of small amount of DNA so there is enough to work with Practical Applications of DNA Technology -Diagnosis of Diseases -Human Gene Therapy -Pharmaceutical Products -Forensic Uses of DNA Technology -Environmental Uses of DNA Technology -Agricultural Uses of DNA Technology Chapter 24 – page 485 The Immune System Nonspecific Defences Skin -Skin glands secrete enzymes Mucus membranes -Digestive system – acids, enzymes -Respiratory system – cilia Phagocytes -White blood cells – phagocytic, engulf bacteria and dead cells -Neutrophils -Monocytes