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Title: Genomics: A new Revolution in Science:


1
  • Genomics A new Revolution in Science
  • An Introduction to promises and Ethical
    Considerations by Genome Alberta

2
  • Genomics A new Revolution in Science
  • This presentation is available
  • at
  • genomealberta.ca

3
Overview
  • Genetics, Mendel to Genomics
  • Genetic Information defined
  • Genomics and Biotechnology
  • Genome Alberta
  • Genome Alberta Projects

4
  • In the 1850s an Austrian monk Gregory Mendel
    started crossing pea varieties
  • He used pollen from some plants to carefully
    fertilize other plants
  • He was able to observe that characteristics are
    inherited in a predictable manner.
  • He determined that alleles of a single trait
    segregate (separate) independently.
  • He observed that the alleles for different traits
    assort independently.
  • This gave rise to a new discipline that we now
    call
  • GENETICS

5
What is Genomics
  • Genetic information is contained with DNA
    (deoxyribonucleic acid) and RNA (ribonucleic
    acids)
  • Each plant, animal or bacteria carries its entire
    genetic code inside almost every one of its cells
  • Genomics is the discipline that aims to decipher
    and understand the entire genetic information
    content of an organism
  • Genomics marked the beginning of a new age in
    biology and medicine

6
Genomics marked the beginning of a new age in
biology and medicine
Working Draft of the human genome sequencing
complete
Rediscovery of Mendel's laws helps establish the
science of genetics
Huntington disease gene mapped to chromosome 4
Sanger and Gilbert derive methods of sequencing
DNA
Genetic and physical mapping
1900
1977
1983
1994-98
2000
2005 (or earlier)
1953
1980
1998
1990
Watson and Crick identify DNA (the double helix)
as the Chemical basis of heredity
DNA markers used to map human disease genes to
chromosomal regions
DNA markers used to map human disease genes to
chromosomal regions
Gene map expected to be complete
Human Genome Projects (HPG) begins-an
international effort to map and sequence all the
genes in the human genome
Source Health Policy Research Bulletin, volume 1
issue2, September 2001
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25,000
metabolite
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Why is it important to know the sequence of
genes?
  • A single base change in a gene in a plant or the
    addition of a single gene from any other source
    to this plant can make a crop herbicide resistant
  • Understanding traits, in particular diseases,
    some inherited diseases results from the change
    of 1 base in a sequence
  • We can use a gene to make a specific product, for
    example insulin

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One change in DNA sequence (mutation) can have a
significant effect!
601 ACGGTGCCCG
CAAAGTGTGG CTAACCCTGA ACCGTGAGGG 601 ACGGTGCCCG
CAAAGTGTGG ATAACCCTGA ACCGTGAGGG
A
B
Herbicide
A
B
27
Simple model of Gene Modification
  • DNA cut with endonuclease
  • Sticky ends created

28
Simple model of Gene Modification
  • Modified section with similar sticky ends
    inserted
  • DNA ligase reattaches new components

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Biotech Crops
  • potential for impact on farm (and biotech
    company) income.
  • potential impact on the environment
  • Reduction of pesticide use
  • Allowed environment friendlier farming practices
    (e.g zero tilling)
  • May be no perceived benefit to the consumer
  • questions about long term safety
  • different and more controversial approach genetic
    engineering

31
Some Interesting Genome Facts
  • Human Genome contains about 3 billion basepairs
  • Corn Genome contains about 2.6 billion basepairs
  • Wheat Genome contains more than 16 billion
    basepairs
  • Not all genetic information encodes for
    functional molecules or life functions

32
Some More Interesting Genomics Facts
  • Humans only have 20 more genes than worms
  • Around 99 of our genes have counterparts in mice
  • Our genetic overlap with chimpanzees is about
    97.5
  • The genetic difference between one person and
    another is less than 0.1
  • But because only a few regions of DNA actively
    encode life functions, the real difference
    between one person and another is only 0.0003
    percent

33
Single Nucleotide Polymorphisms (SNPs)
  • Major discovery of human genome project was
    single nucleotide polymorphisms (SNPs) points in
    genome where 2 or more alternative alleles are
    found in gt1 of population
  • 93 genes have SNPs
  • 40 will alter an amino acid
  • SNPs may have important consequences for
    health/disease

34
SNPs- The International HapMap Project
  • Goal To develop a haplotype map of the human
    genome, the HapMap, which will describe the
    common patterns of human DNA sequence variation
  • Outcome Key resource for researchers to use to
    find genes affecting health, disease, and
    responses to drugs and environmental factors
  • Who Ten centers in Canada, China, Japan,
    Nigeria, the United Kingdom, and the United
    States
  • How much US 200M
  • When Start Oct 2002

35
International Consortium Completes Map

                                 
International Consortium Completes Map Of Human
Genetic Variation New Tool Speeding the Discovery
of Genes for Common Diseases
                                        SALT LAKE
CITY, Wed., Oct. 26, 2005 - The International
HapMap Consortium today published a comprehensive
catalog of human genetic variation, a landmark
achievement that is already accelerating the
search for genes involved in common diseases,
such as asthma, diabetes, cancer and heart
disease.
36
SNPs
  • These small differences can make a big
    difference, it determines whether you are short
    or tall, hair and skin color and..
  • These differences are sufficient to make some
    healthy and others very sick
  • It can determine whether you get cancer or not.
    Women who carry a genetic variation known as
    BRCA-1 are seven times more likely to get breast
    cancer
  • If you are missing three nucleotides (CTT) at a
    specific spot in your genome you have Cystic
    Fibrosis

37
Traditional vs Personalized Medicine
  • Traditional medicine
  • Educated guess on which treatment might be most
    beneficial
  • Personalized Medicine
  • the use molecular analysis to manage a patients
    disease by helping physicians and patients choose
    the disease management approaches likely to work
    best in the context of a patients genetic and
    environmental profile.

38
Traditional vs Personalized Medicine
  • Need for Personalized medicine
  • Every Year over 106,000 people in the US die from
    adverse reaction to correctly prescribed doses of
    drugs
  • Another 2.2million suffer serious but not deadly
    side effects

39
Goals for Personalized Medicine
  • Identify genetic differences between people that
    affect drug response
  • Develop genetic tests that predict an
    individuals response to a drug
  • Tailor medical treatments to the individual
  • Increase effectiveness
  • Minimize adverse side effects

40
  • Wednesday, Oct 19, 2005Pivotal Herceptin Data
    in the New England Journal of Medicine Showed
    Significant Improvement in Disease-Free Survival
    in Early-Stage HER2-Positive Breast
    Cancer-- Interim Analysis of Two Phase III
    Trials Showed That Adding Herceptin to
    Chemotherapy Reduced the Risk of Breast Cancer
    Recurrence by 52 Percent --

41
Calgary Herald. Monday, Feb 12, 2007
42
Identification of Genetic Susceptibility to
Disease
  • Identify genetic differences between people that
    predict susceptibility to disease
  • Develop genetic tests that predict whether an
    individual will develop a particular disease
  • Offer treatment to prevent or delay onset of
    disease

43
Future Research Fixing disease at the DNA level
  • Identify genetic abnormality that causes disease
  • Introduce new genetic material that corrects or
    bypasses the abnormality
  • Gene Therapy
  • Isolate piece of DNA containing gene with normal
    function
  • Introduce into gene transfer tool
  • Transfer gene into individual with disease

44
Accumulation of Sequence Information
45
Sequencing Cost Have been Dramatically Reduced
  1. 10,000
  2. 100
  3. 1
  4. 1 cts
  5. 0.1 cts
  6. 0.001 cts
  7. 0.00001 cts

46
Some More Interesting Facts
  • Human Genome
  • Took 12 years to complete at a cost of US3
    Billion
  • Mouse Genome
  • Took 3 years to complete at a cost of US 300
    million
  • Bovine Genome
  • Took about 1 year at an estimated cost of US
    30 million

47
Availability of Personal Genetic Information
Poses Challenges
  • Privacy
  • Confidentiality
  • Discrimination
  • Psychological Impact

48
Something to Think About
  • Who should have access to stored genetic
    information? Who owns and controls it?
  • How can families resolve conflict when some
    members want to be tested for a genetic disorder
    and others do not?
  • Should employers be able to require job
    applicants to take genetic tests as a condition
    for employment?
  • How would you feel if you tested positive for a
    genetic disorder. How would you feel if you
    tested negative?

49
Privacy and Confidentiality of Genetic Test
Results
  • Clinical test results are normally included in a
    persons medical records, this could have serious
    complications
  • For example, when applying for medical, life, or
    disability insurance, people may be asked to
    reveal their medical history.

50
Genome Alberta
  • Independent not-for-profit corporation
  • One of the six regional Genome Centers supported
    by Genome Canada
  • Genome Canada receives its funds from Industry
    Canada
  • Support research in plant, animal and human
    genomics, bioinformatics, instrumentation
    development and bioethics
  • Much more information is available at
    www.genomalberta.ca
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