lecture 20 Flashcards

genetic manipulation of mammalian animals and cells transgenics

1
Q

What is transgenesis?

A

the process of transferring genes to animals

transgenics refers to a gain of function

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2
Q

What is a transgenic animal?

A

an animal that carries a transgene

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3
Q

What is a transgene?

A

the foreign gene

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4
Q

What do you start with if you are trying to make a whole animal with a mutation? Why is that significant?

A

fertilised egg

  • supposedly male pro-nucleus is slightly larger than female pro-nucleus
  • haploid nucleus of the male has been transferred by fertilization into the centre of the egg
  • female egg of all mammals is frozen at metaphase II of meiosis
  • half extruded in a polar body
  • two halves of the nucleus join, create a spindle and then undergo cell division to create two cells
  • if you inject DNA/RNA into one of the haploid genomes when they mount up on the spindle to undergo their first cell division every cell after that will have the DNA
  • if you miss that time point, e.g. into one cell of a two cell embryo, only half will have the insert
  • therefore critical to be injected into a haploid genome
  • before spindling
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5
Q

What is the transgenic technique?

A
  • mate mice
  • flush out fertilised eggs from oviduct
  • have about 12 hours in mice
  • inject transgene construct into one pronucleus
  • culture blastocysts
  • implant into pseudopregnant host female
  • prepare genomic DNA from tails of offspring
  • analyse for presence of transgene e.g. by PCR analysis
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6
Q

What are properties of the transgene?

A
  • inject picolitres of the gene construct - not much, but each has many copies of the gene
  • insert into only one site in the genome
  • the transgene randomly integrates into the host cell genome
  • transgene can become stably integrated into the germ line
  • once you’ve created the animal you can create a line of animals
  • can freeze down sperm of the animals
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7
Q

What is random integration of the transgene?

A
  • the transgene can integrate anywhere in the genome
  • if it integrates into the promoter region of another gene it will interrupt the function of the gene: increase, decrease or no effect of transgene expression may lead to cell proliferation, apoptosis etc
  • if it integrates into gene it may generate a defective protein, may lead to cell proliferation, apoptosis etc
  • all of this can lead to insertional mutagenesis: generation of mutations in DNA by insertion of one or more bases
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8
Q

How do we get tissue specific gene expression?

A

transgene construct: e.g. rat insulin promoter + growth factor

sometimes these promoters are leaky because you aren’t taking the full promoter

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9
Q

What is pharming for farmaceuticals?

A
  • pronuclear injection current method e.g. pigs, rabbits, goats, cows, rats, mice, sheep
  • transgene directed to mammary gland, blood cells, bladder cells. Milk, blood, urine (or egg white in chicks)
  • large daily output, post-translational processing, low capital cost, easy access to transgene protein
  • mammary gland promoters: beta-lactoglobulin, beta-casein, alpha s 1-casein, whey acidic protein
  • generate transgenic construct: beta-lactoglobulin + transgene
  • inject into fertilised egges
  • generate line of sheep expressing transgene protein into milk
  • collect and fractionate milk
  • purify transgene protein

examples of human proteins secreted into milk of transgenic animals =

  • antithrombin III in goat for thrombosis (GTC biotherapeutics USA)
  • tPA in goat for thrombosis (PPL therapeutics UK)
  • A-antitrypsin in sheep for emphysema (“ “)
  • Factor IX in sheep for haemophilia (“ “ )
  • polyclonal antibodies in cattle for vaccines (hematech USA)

animals as bioreactors

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10
Q

How can we use an animal model of human disease?

A

interleukin-6 (IL-6)

  • important cytokine for blood development and immune system function
  • IL-6 levels are high in inflammation, infection, or trauma induced disorders of the central nervous system

to understand function of IL-6:

  • generate a transgenic animal that over-expresses IL-6 in the brain (animal model)
  • transgene injected into pronucleus (brain-specific promoter and IL-6 cDNA)
  • result:
    • animals have nerver damage – severity correlates to level of IL-6
    • this model demonstrates that IL-6 has a role in the pathology of degeneration in the brain
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11
Q

How can we use transgenics to improve livestock?

A

Selective breeding has been done for centuries
transgenics fast tracks this process

e.g. transgenics that over-express growth hormone vs selectively breeding naturally big pigs

results:
- increase in rate of growth
- decreased amount of feed required per unit weight gain
- reduced levels of body fat lipids, cholesterol, lower saturated and unsaturated fats
(pigs normally only have growth hormone for two months)
also:
- reduced reproductive performance
- arthritis
- gastric ulcers
- renal disease
- premature death

these technologies are good but they have dark and light sides

  • be informed
  • just printing the good side is not a fair assessment
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12
Q

What are disadvantages of using animals as bioreactors?

A
  1. unexpected or undesired effects of the transgene
    - leaky expression
  2. effect of the transgene on the health of the animal
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13
Q

How do transgenics compare to gene targeting?

A

transgenics vs gene-targeted

  • technique to transfer transgene: pronuclear injection vs electroporation
  • integration type: random vs site-specific/targeted
  • is foster mother required?: yes – grow to blastocyst stage, transfer to host uterus, one generation for effect of transgene vs yes – inject targeted cells into host blastocyst, transfer to host uterus. Breed +/- to generate -/-. Analyse phenotype of -/-
  • detect transgene: DNA analysis (both)
  • germline?: yes (both)
  • species: all vertebrates vs mice
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14
Q

How do the efficiencies of different techniques compare?

A
  • transgenic: 60-80%, relies on construct integrating randomly in the zygote
  • conventional gene-targeting: 1-6%, homologous recombination, ES cells
  • zinc finger nucleases: 1-20%, DNA mis-repair, zygote
  • CRISPR/Cas system: 1-20%, DNA misrepair, zygote
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