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Transgenic animals

      Hoza, A.S
   BLS 209 Lecture
What is a transgenic animal?

• An animal contains a foreign gene (genes)
introduced purposely by human intervention

•Transgenic animals are altered so that their DNA
produce proteins that normally they would not
produce
History of transgenic animal production
    1970's, first transgenic mice via viral
   infection, but not germline transmission

  1980's, first transgenic mice via microinjection,
  the most popular technique

  1985, first transgenic rabbits, sheep, pigs and
  cattle

  80-90, commercial transgenic services, via
  transgenic facility

  1990's, transgenic farm animal companies as
  bioreactors and organ donors
Different ways to create transgenic animals
Target gene – transgene

  Promoter/enhancer - when, where, how much

  Coding sequence - coding the specific protein

  ploy A detail - mRNA stability




             Transgene Structure
Gene transfer methods
1. Microinjection of recombinant DNA into the male
   pronucleus of an in vitro fertilized egg.

2. Embryonic stem cell transfer (ES).

Other methods:
  1. Chemical or

  2. Viral delivery into ES cells, or homologous
     recombination with ES cells.
Microinjection

• Inject DNA molecules (transgenes) directly into
male pronucleus

• Most popular technology, commercial available

• Success rates range from 10-30% depending on
skills and constructs

•Efficiency is not related to the copies of transgenes
injected
Microinjection

• The technique can be applied to other species

• No theoretical limit for the size of the construct

• Overall efficiency is still low, particularly for farm
animals

• Tandem repeat of gene constructs (head-tail)

• High frequency of mosaic

• Initial investment is high
Virus mediated gene transfer
• Earliest method for successful gene transfer in
mammals

• Virus has transfection property

• Killed virus is replication defective

• The virus gene is replaced with transgene gene

• The transgene is delivered to the host cell by
transfection (gene therapy)

• Can be used to transfect a wide range of cells, e.g.,
ES cells
Virus mediated gene transfer
•Direct transfection of embryos has resulted
nongermline transgenics

• ES cells transfection has resulted in germline
transgenics

• Has succeeded in chickens and fish

• Transfecting oocytes resulted in 100% transgenics

• Only small transgene construct is usable (8 kb or
less)
• More research is needed on the safety of the
method
Embryonic stem cells

•Used mostly when trying to target a transgene to
a specific site in the genome.

• Derived from ICM of blastocyst stage embryo

• Divide in vitro indefinitely without differentiation

• Contribute to development of the fetus in any
tissues, organs (germline)

• Has the potential to give rise to all tissues
ES cells

• May be transfected with transgene or with
genes removed (knockout) or inserted prior to
microinjection

• Has revolutionized genetics, development,
immunology and cancer research in mice
Steps for ES Cell Manipulation.
Approaches to using ES cells to create transgenic
                   animals.
 1. The transgene can be microinjected into the
    ES cells
 2. can be introduced by a virus,
 3. Chemical (e.g calcium phosphate or rubidium
    chloride
 4. by using homologous recombination.
Nuclear transfer

• Creation of Dolly

• Somatic cells be transfected, or genetically altered
prior to NT

• 100% efficiency of any progeny

• Low efficiency

• Abnormal development
Screening for Transgenic Positives


• Identification of transgene integration - DNA

• Detect transgene transcription - mRNA

• Detect transgene expression - protein
TRANSGENIC ANIMAL CLASSIFICATION
Five major categories:
   1. disease models
   2. transpharmers
   3. xenoplanters
   4. food sources
   5. scientific models

1.Disease models:

  animals that have been modified to exhibit the
  symptoms and progression of a particular disease,
  so that treatments for that disease can be tested
  on them (e.g oncomouse, AIDS mouse etc)
2.Transpharmers:

  animals modified to express a particular
  protein or suite of proteins in their milk to avoid
  animal sacrifice when obtaining the drug.

  The proteins can be purified to produce
  medicines and hormones to treat humans, or
  can possibly be administered as medicinal milk
  itself.
Mice- commonly used to test the transpharming
transgene first.

The transgenic procedure is promising, but very
expensive, and still has a low success rate especially
for larger farm animals.

   A mouse engineered in 1987 to express the clot
   dissolver drug tissue plasminogen activator (tPA)

   In 1990, human alphaantitrypsin, an inhibitor used to
   treat emphysema, was produced in the mouse’s milk.

   1997 at the New Technology Institute- human alpha-
   lactalbumin in mouse’s milk
Larger animals like sheep, goats, and cows are the targets
for large-scale transpharming.

   E.g 6 transgenic lambs for Roslin Institute - created in
   1997 to produce a human clotting factor in their milk.

    The first transpharmer goats were produced in 1991 at
   the Tufts University School of Veterinary Medicine to
   produce tissue plasminogen activator, a clotdissolving
   drug.

    transpharmer goats were produced in 1999 using
   SCNT       contained high levels of human antithrombin
   III.
The first transgenic cow (Gen Pharm Intern, California),
dubbed “Herman”, and his first transgenic offspring were
bred at Gen Pharm’s lab (Netherlands)

Two calves were produced by microinjection of DNA into
embryos that were then implanted in surrogate mothers and
born alive.

One of these cows was female                the transgene
rearranged itself so that a portion of the lactoferrin cDNA was
deleted.

The other calf was male, later called “Herman.” He and his
offspring contained the correctly arranged gene for human
lactoferrin.
3. Xenoplanters:
   animals that have been engineered to not
   express the foreign antigens that normally
   prevent the transplantation of their organs into
   humans.

4. Food sources:
    animals that grow bigger or faster to produce
   more food in a shorter amount of time with fewer
   resources. E.g superpig, superfish
5. Scientific models:
      animals producing more or less of a
      particular protein than usual,

    Study that protein’s purpose in biological
    mechanisms or development          applied to
    humans. E.g ANDi first transgenic monkey
TRANSGENIC ETHICS
1. Animal Rights Versus Animal Welfare

2. Right to meddle in the genomes of living beings
   Transgenesis- a logical step beyond selective
   breeding,
      open doors past what we previously have
      known to cure diseases!!??
      possibly end world hunger entirely!!!??

Transgenic Art - Creating monsters!!! E.g “Alba,” the
rabbit that glows under UV light!!!!???
Eduardo “transgenic art.” refers to animals and plants with a
planned genome intended to express an artistic idea
symbolized by the proteins they code for.
4. Animal Death Versus Human Lives Saved
    low success rate in creating transgenic animals.

5. Transgenic Animals and the Environment
    decrease of genetic variability within that species

   Transgenic animals are not “more fit” than their “normal”
   cousins.

 6. Transgenic Oversight
     Transgenic experimentation should be as
     humane as possible.

  7. Religions and Transgenic Ethics
Applications of transgenic farm animals

• Agricultural applications

• Bioreactors

• Organ/cell/tissue donors

• Basic research/disease model
Transgenic animals

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Transgenic animals

  • 1. Transgenic animals Hoza, A.S BLS 209 Lecture
  • 2. What is a transgenic animal? • An animal contains a foreign gene (genes) introduced purposely by human intervention •Transgenic animals are altered so that their DNA produce proteins that normally they would not produce
  • 3. History of transgenic animal production 1970's, first transgenic mice via viral infection, but not germline transmission 1980's, first transgenic mice via microinjection, the most popular technique 1985, first transgenic rabbits, sheep, pigs and cattle 80-90, commercial transgenic services, via transgenic facility 1990's, transgenic farm animal companies as bioreactors and organ donors
  • 4. Different ways to create transgenic animals Target gene – transgene Promoter/enhancer - when, where, how much Coding sequence - coding the specific protein ploy A detail - mRNA stability Transgene Structure
  • 5. Gene transfer methods 1. Microinjection of recombinant DNA into the male pronucleus of an in vitro fertilized egg. 2. Embryonic stem cell transfer (ES). Other methods: 1. Chemical or 2. Viral delivery into ES cells, or homologous recombination with ES cells.
  • 6. Microinjection • Inject DNA molecules (transgenes) directly into male pronucleus • Most popular technology, commercial available • Success rates range from 10-30% depending on skills and constructs •Efficiency is not related to the copies of transgenes injected
  • 7. Microinjection • The technique can be applied to other species • No theoretical limit for the size of the construct • Overall efficiency is still low, particularly for farm animals • Tandem repeat of gene constructs (head-tail) • High frequency of mosaic • Initial investment is high
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  • 10. Virus mediated gene transfer • Earliest method for successful gene transfer in mammals • Virus has transfection property • Killed virus is replication defective • The virus gene is replaced with transgene gene • The transgene is delivered to the host cell by transfection (gene therapy) • Can be used to transfect a wide range of cells, e.g., ES cells
  • 11. Virus mediated gene transfer •Direct transfection of embryos has resulted nongermline transgenics • ES cells transfection has resulted in germline transgenics • Has succeeded in chickens and fish • Transfecting oocytes resulted in 100% transgenics • Only small transgene construct is usable (8 kb or less) • More research is needed on the safety of the method
  • 12. Embryonic stem cells •Used mostly when trying to target a transgene to a specific site in the genome. • Derived from ICM of blastocyst stage embryo • Divide in vitro indefinitely without differentiation • Contribute to development of the fetus in any tissues, organs (germline) • Has the potential to give rise to all tissues
  • 13. ES cells • May be transfected with transgene or with genes removed (knockout) or inserted prior to microinjection • Has revolutionized genetics, development, immunology and cancer research in mice
  • 14. Steps for ES Cell Manipulation.
  • 15. Approaches to using ES cells to create transgenic animals. 1. The transgene can be microinjected into the ES cells 2. can be introduced by a virus, 3. Chemical (e.g calcium phosphate or rubidium chloride 4. by using homologous recombination.
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  • 17. Nuclear transfer • Creation of Dolly • Somatic cells be transfected, or genetically altered prior to NT • 100% efficiency of any progeny • Low efficiency • Abnormal development
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  • 19. Screening for Transgenic Positives • Identification of transgene integration - DNA • Detect transgene transcription - mRNA • Detect transgene expression - protein
  • 21. Five major categories: 1. disease models 2. transpharmers 3. xenoplanters 4. food sources 5. scientific models 1.Disease models: animals that have been modified to exhibit the symptoms and progression of a particular disease, so that treatments for that disease can be tested on them (e.g oncomouse, AIDS mouse etc)
  • 22. 2.Transpharmers: animals modified to express a particular protein or suite of proteins in their milk to avoid animal sacrifice when obtaining the drug. The proteins can be purified to produce medicines and hormones to treat humans, or can possibly be administered as medicinal milk itself.
  • 23. Mice- commonly used to test the transpharming transgene first. The transgenic procedure is promising, but very expensive, and still has a low success rate especially for larger farm animals. A mouse engineered in 1987 to express the clot dissolver drug tissue plasminogen activator (tPA) In 1990, human alphaantitrypsin, an inhibitor used to treat emphysema, was produced in the mouse’s milk. 1997 at the New Technology Institute- human alpha- lactalbumin in mouse’s milk
  • 24. Larger animals like sheep, goats, and cows are the targets for large-scale transpharming. E.g 6 transgenic lambs for Roslin Institute - created in 1997 to produce a human clotting factor in their milk.  The first transpharmer goats were produced in 1991 at the Tufts University School of Veterinary Medicine to produce tissue plasminogen activator, a clotdissolving drug.  transpharmer goats were produced in 1999 using SCNT contained high levels of human antithrombin III.
  • 25. The first transgenic cow (Gen Pharm Intern, California), dubbed “Herman”, and his first transgenic offspring were bred at Gen Pharm’s lab (Netherlands) Two calves were produced by microinjection of DNA into embryos that were then implanted in surrogate mothers and born alive. One of these cows was female the transgene rearranged itself so that a portion of the lactoferrin cDNA was deleted. The other calf was male, later called “Herman.” He and his offspring contained the correctly arranged gene for human lactoferrin.
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  • 28. 3. Xenoplanters: animals that have been engineered to not express the foreign antigens that normally prevent the transplantation of their organs into humans. 4. Food sources:  animals that grow bigger or faster to produce more food in a shorter amount of time with fewer resources. E.g superpig, superfish
  • 29. 5. Scientific models: animals producing more or less of a particular protein than usual, Study that protein’s purpose in biological mechanisms or development applied to humans. E.g ANDi first transgenic monkey
  • 30. TRANSGENIC ETHICS 1. Animal Rights Versus Animal Welfare 2. Right to meddle in the genomes of living beings Transgenesis- a logical step beyond selective breeding, open doors past what we previously have known to cure diseases!!?? possibly end world hunger entirely!!!?? Transgenic Art - Creating monsters!!! E.g “Alba,” the rabbit that glows under UV light!!!!???
  • 31. Eduardo “transgenic art.” refers to animals and plants with a planned genome intended to express an artistic idea symbolized by the proteins they code for.
  • 32. 4. Animal Death Versus Human Lives Saved low success rate in creating transgenic animals. 5. Transgenic Animals and the Environment decrease of genetic variability within that species Transgenic animals are not “more fit” than their “normal” cousins. 6. Transgenic Oversight Transgenic experimentation should be as humane as possible. 7. Religions and Transgenic Ethics
  • 33. Applications of transgenic farm animals • Agricultural applications • Bioreactors • Organ/cell/tissue donors • Basic research/disease model