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
3Overview
- 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
5What 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
6Genomics 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
7(No Transcript)
8(No Transcript)
9(No Transcript)
1025,000
metabolite
11(No Transcript)
12(No Transcript)
13(No Transcript)
14(No Transcript)
15(No Transcript)
16(No Transcript)
17(No Transcript)
18(No Transcript)
19(No Transcript)
20(No Transcript)
21(No Transcript)
22(No Transcript)
23(No Transcript)
24Why 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
25(No Transcript)
26One 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
27Simple model of Gene Modification
- DNA cut with endonuclease
- Sticky ends created
28Simple model of Gene Modification
- Modified section with similar sticky ends
inserted - DNA ligase reattaches new components
29(No Transcript)
30Biotech 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
31Some 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
32Some 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
33Single 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
34SNPs- 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
35International 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.
36SNPs
- 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
37Traditional 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.
38Traditional 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
39Goals 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 --
41Calgary Herald. Monday, Feb 12, 2007
42Identification 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
43Future 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
44Accumulation of Sequence Information
45Sequencing Cost Have been Dramatically Reduced
- 10,000
- 100
- 1
- 1 cts
- 0.1 cts
- 0.001 cts
- 0.00001 cts
46Some 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
47Availability of Personal Genetic Information
Poses Challenges
- Privacy
- Confidentiality
- Discrimination
- Psychological Impact
48Something 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?
49Privacy 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.
50Genome 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