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123biotech 07

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100% found this document useful (1 vote)
111 views32 pages

123biotech 07

biotech

Uploaded by

Hema Rawindran
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPT, PDF, TXT or read online on Scribd
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PowerPoint Lectures for

Introduction to Biotechnology, Second Edition


William J.Thieman and Michael A.Palladino

Chapter 7
Animal Biotechnology

Lectures by Lara Dowland

Copyright © 2009 Pearson Education, Inc.


Chapter Contents

• 7.1 Introduction to Animal Biotechnology


• 7.2 Animals in Research
• 7.3 Clones
• 7.4 Transgenic Animals
• 7.5 Producing Human Antibodies in
Animals

Copyright © 2009 Pearson Education, Inc.


7.1 Introduction to Animal Biotechnology

• Genetically engineered animals can be used to


– Develop new medical treatments
– Improve our food supply
– Enhance our understanding of all animals, including
humans
• Presents tough scientific and ethical challenges

Copyright © 2009 Pearson Education, Inc.


7.2 Animals in Research

• Animal Models
– Many genetic and physiological similarities exist between
animals and humans
– Research using animals has been the key to most
medical breakthroughs in the past century
• Polio vaccine
• Cataract surgery techniques
• Dialysis
– Biotechnology has developed 111 USDA-approved
veterinary biologics and vaccines

Copyright © 2009 Pearson Education, Inc.


7.2 Animals in Research

• FDA regulations state that new drugs, medical


procedures, and cosmetic products must pass
safety tests
– Involves phase testing
• Conduct a significant number of trials on cell cultures, in
live animals, and on human research participants

Copyright © 2009 Pearson Education, Inc.


7.2 Animals in Research

• Animals most often used are


– Purebred mice and rats
• Other species used include
– Zebrafish, fruit flies, nematodes
• Dogs, monkeys, chimpanzees, cats make up less
than 1% of total number of research animals

Copyright © 2009 Pearson Education, Inc.


7.2 Animals in Research

• Alternatives to Animal Models


– Cell culture and computer-generated models
• Cell Culture
– Preliminary screen to check the toxicity of substances
– Can answer fundamental questions about biology
– Cannot provide information about potential impacts on
entire living organism

Copyright © 2009 Pearson Education, Inc.


7.2 Animals in Research

• Computer Models
– Simulate specific molecular and chemical structures and
their interactions
– Limited by programming and knowledge of how the
physiological system works

Copyright © 2009 Pearson Education, Inc.


7.2 Animals in Research

• Regulation of Animal Research


– Federal Animal Welfare Act set standards regarding the
housing, feeding, cleanliness, and medical care of
research animals
– Institutional Review Boards are present at each
institution; researcher must prove the need to use
animals, select the most appropriate species, and devise
a plan for using as few animals as possible

Copyright © 2009 Pearson Education, Inc.


7.2 Animals in Research

• Regulation of Animal Research


– To receive funding from the NIH, the FDA, or the CDC,
researchers must follow standards of care set out in The
Guide for the Care and Use of Laboratory Animals

Copyright © 2009 Pearson Education, Inc.


7.2 Animals in Research

• Veterinary Medicine as Clinical Trials


– Veterinarians also participate in research
– Information gleaned from one species may be applied to
another
• BRCA1 gene in humans is similar to BRCA1 gene in dogs
• Cancer treatments cross between species

Copyright © 2009 Pearson Education, Inc.


7.2 Animals in Research

• Bioengineering Mosquitoes to Prevent Malaria


– Prevents parasite from transversing the midgut
– Prevents parasite from entering salivary gland

Copyright © 2009 Pearson Education, Inc.


7.3 Clones

• Embryo Twinning – splitting embryos in half


– First step toward cloning
– Procedure is relatively easy, but has limited applications
• Results in identical twins, but exact nature of those twins is
the result of a mix of genetic material from two parents
• Dolly was created from an adult cell
– Exact duplicate of an adult with known characteristics

Copyright © 2009 Pearson Education, Inc.


7.3 Clones

• Creating a Clone from an Adult


– DNA from donor cell must be inserted into an egg
– Egg is prepared by enucleation
• Pipette suctions out the nucleus
– DNA from donor cell put into egg cell
– Embryo is transferred to a surrogate mother for gestation
– Sheep, pigs, goats, cattle, and a gaur have been cloned

Copyright © 2009 Pearson Education, Inc.


7.3 Clones

Copyright © 2009 Pearson Education, Inc.


7.3 Clones

• The Limits to Cloning


– Donor cell must come from a living organism
– Clones are not exactly identical
• Shaped by experiences and environments
– Present success rate is quite low
• Dolly was result of 277 efforts
• Cc was only success out of 87 implanted clone embryos
– Clones may be old before their time
• Shortened telomeres

Copyright © 2009 Pearson Education, Inc.


7.3 Clones

• The Future of Cloning


– Still a young science and subject to much
experimentation
– Not a practical solution to transplant organ shortages
• Profound ethical questions
• Would take years for clone to be mature enough to donate
organs

Copyright © 2009 Pearson Education, Inc.


7.3 Clones

• The Future of Cloning


– Clones can be used in medical research where their identical
genetics makes it easier to sort out results of treatments
– Clones may provide a unique window on the cellular and
molecular secrets of development, aging, and diseases
– Clones could sustain breeding population of endangered
species
– Cloning can be used to directly improve agricultural production

Copyright © 2009 Pearson Education, Inc.


7.4 Transgenic Animals

• Introducing New Genetic Material into Animals


– Retrovirus-mediated transgenics
• Infecting mouse embryos with retroviruses before the
embryos are implanted
• Size of transgene (transferred genetic material) is limited
– Pronuclear microinjection
• Introduces the transgene DNA at the earliest possible
stage of development of the zygote
• DNA is injected directly into nucleus of egg or sperm

Copyright © 2009 Pearson Education, Inc.


7.4 Transgenic Animals

Copyright © 2009 Pearson Education, Inc.


7.4 Transgenic Animals

• Introducing New Genetic Material into Animals


– Embryonic stem cell method
• Embryonic stem cells are mixed with DNA and will absorb
the DNA
– Sperm-mediated transfer
• Uses “linker proteins” to attach DNA to sperm cells
– Gene guns can also be used on animal cells

Copyright © 2009 Pearson Education, Inc.


7.4 Transgenic Animals

• Can use gene transfer to improve the productivity


of livestock
– Introduce genes for faster growth rates or leaner growth
patterns = quicker to market and healthier meat
– Chickens
– Dairy industry
– EnviroPig

Copyright © 2009 Pearson Education, Inc.


7.4 Transgenic Animals

• Transgenic Animals as Bioreactors


– Whole animals can serve as bioreactors to produce
proteins
– Gene for a desired protein is introduced via transgenics
to the target cell
– By using cloning techniques, cell is raised to become an
adult animal
– Produce milk or eggs that are rich in the desired protein

Copyright © 2009 Pearson Education, Inc.


7.4 Transgenic Animals

Copyright © 2009 Pearson Education, Inc.


7.4 Transgenic Animals

• Knockouts: A Special Case of Transgenics


– Mice that have been genetically engineered so that a
specific gene is disrupted
– DNA is modified and added to the embryonic stem cells,
where it recombines with the existing gene on a
chromosome
• Called homologous recombination
– Modified ES cells are introduced into normal embryo and
embryo is implanted into a mother

Copyright © 2009 Pearson Education, Inc.


7.4 Transgenic Animals

• Knockouts: A Special Case of Transgenics


– The mouse pup is a chimera – some cells are normal
and some are knockouts
– Two generations of breeding are required to produce
complete knockouts
• Knock-in animals – have a human gene inserted to
replace their own counterpart

Copyright © 2009 Pearson Education, Inc.


7.4 Transgenic Animals

Copyright © 2009 Pearson Education, Inc.


7.4 Transgenic Animals

• One limitation in the therapeutic use of antibodies


is the production of a specific antibody in large
quantities

Copyright © 2009 Pearson Education, Inc.


7.5 Producing Human Antibodies in
Animals
• Production of Monoclonal Antibodies (Mabs)
– Mouse or rat inoculated with the antigen (Ag) to which an
antibody is desired
– Spleen harvested after an immune response is produced
– Spleen cells are fused with a specialized myeloma cell
line that no longer produces an antibody of its own
• Myeloma is an antibody-secreting tumor

Copyright © 2009 Pearson Education, Inc.


7.5 Producing Human Antibodies in
Animals
• Production of Monoclonal Antibodies (Mabs)
– The resulting hybridoma (fused cells) grows continuously
and rapidly like the tumor and produces the antibody
specified by the spleen cells
• Mabs used to treat
– Cancer
– Heart disease
– Transplant rejection

Copyright © 2009 Pearson Education, Inc.


7.5 Producing Human Antibodies in
Animals

Copyright © 2009 Pearson Education, Inc.


7.5 Producing Human Antibodies in
Animals
• Mouse hybridomas cause the HAMA response
– Human antimouse antibody response
• Working to solve this problem by creating
antibodies in different organisms

Copyright © 2009 Pearson Education, Inc.

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