Title: The Human Genome
1The Human Genome
- the human genome consists of 3 billion bp and
30,000-35,000 genes (haploid state) - it would fill about 150,000 phone book pages with
As, Ts, Gs, and Cs - a disorder can be caused by variation in one or
more base pairs (among the 3 billion) - the challenge is partly one of scale (needle in a
haystack)
2The Human Genome
- Human genome 3 billion bp
- Average chromosome 150 million bp
- Average gene 50 thousand bp
- Average coding sequence 3 thousand bp
- Unit of the genetic code 3 bp
- Genetic variation variable
3The Human Genome Project
- the largest biomedical research project ever
- an international project that is ahead of
schedule and under budget - from its beginning has set aside funds for its
ethical, legal, and social implications
(ELSI)--the largest single amount of money ever
devoted to bioethics
4The Human Genome Project
- About 90 of the human genome has been sequenced
(the alphabet, so to speak - see web site).
- the sequence is a vital tool, but by itself will
have little impact - the real impact will come when we figure out
how the words/sentences are formed, and what they
mean
5The Human Genome Project and Related Technologies
- impact on the practice of genomic medicine
- impact on health (and health promotion/disease
prevention) - impact on society
6Genomic Medicine
- about the interface between genomic and
environmental (multifactorial) risk and
protective factors - about conditions (e.g., heart disease, cancer,
Alzheimer disease, mood disorders, etc.) caused
or prevented, in part, by one or more variations
in DNA - variations is a better word than mutations
7Genomic Medicine
- These conditions
- are also of great importance to individuals and
families who are affected by them - are quite common (affect virtually everyone)
- cause genomics play a considerable role in health
care and in society, in general
8Genomic Medicine
- Thus far, most success in identifying genomic
contributions to common disorders has been for
low frequency, high penetrance alleles for
example - HNPCC (colon cancer)
- BRCA1 and 2 (breast and ovarian cancer)
- MODY 1,2,3 (diabetes)
- Alpha-synuclein (Parkinson Disease)
9Genomic Medicine
- But, on a population basis, most genomic
contributions to common disorders are from high
frequency, low penetrance alleles for example - APC I1307K and colon cancer
- ApoE and Alzheimer disease
- Factor V Leiden and thrombosis
- CCR5 and HIV resistance
10Genetic Variation and Disease
- Mendelian disorders are relatively rare--the DNA
variation is necessary and sufficient to cause
considerable phenotypic effects. - Complex disorders are caused by common DNA
variations--any one of which may not be necessary
or sufficient to produce a phenotypic effect,
i.e., each variation has a small phenotypic
effect.
11The Practice of Genomic Medicine
- Conditions
- Health Care and Health Care Providers
- Public Health Genetics
12The Practice of Genomic Medicine
- Many chronic conditions are common enough such
that genomic health care will be provided for the
most part by primary care professionals from many
health disciplines, with involvement of genomic
health care specialists when appropriate/necessary
.
13The Practice of Genomic Medicine
- The practice of genomic medicine will change
health care by - providing a better understanding of non-genetic
(environmental) factors in health and disease - providing a better understanding of the natural
history of most rare and common conditions - emphasizing health maintenance rather than
disease treatment - allowing for genetic therapies (engineering)
14The Practice of Genomic Medicine
- These conditions are common enough such that
- genomics has and will continue be a primary focus
for public health - might genomics be to public health in the 21st
century what infectious diseases were to public
health in the previous centuries
15The Practice of Genomic Medicine
- The practice of genomic medicine will
- change the face of medicine and health care by
providing knowledge of individual genomic
predispositions - enable population-based screening, and more
individualized testing for rare and common
disorders with a genomic component - enable the practice of pharmacogenomics and other
types of more individualized therapies
16The Practice of Genomic Medicine
- Pharmacogenomics will allow for
- a wide variety of new medicines
- more individualized use of new medications based
on genetic variations/effects and side effects
17Medical Genetics Time Line
- 2000 and beyond
- functional genomics and pathogenomics
- genomic-based risk prediction
- individualized therapy for genomic
disorders/gene therapy - pharmacogenetics
- public health genetics
18Genetic Medicine and Research
- In terms of research
- the common, chronic conditions have and will
continue to be of considerable interest because
of their large impact on health and health care - in the next few decades, genomics will answer
many basic biomedical questions, and provide
better screening and testing methods, and
interventions (many of them pre-symptomatic)
19Genomics and Other Phenotypic (Non-Disorder)
Characteristics
- The study of genomics will probably include
characteristics that most do not see as
diseases, and many do not consider to be innate
(intelligence, growth and development, sexual
orientation, alcoholism, violent behavior,
happiness-sadness, confidence-anxiety,
altruism-greed)
20Genomics and Society
- Genomics will change our lives by
- allowing individuals and families (and maybe
others) to know about their health and disease
predispositions, and other characteristics and
attributes - allowing for policy development/decisions at the
local, state, national and international levels - showing that we are all MUTANTS!
- showing how similar we are in some ways and
different in others
21Genomics and Society
- Genomics may change our lives through
- social stratification (employment, marital
status, emigration status, etc.) - genetic/genomic engineering
- cloning
- euphenics (modifications in phenotype) rather
than eugenics - discrimination against individuals and groups
22Genomics and Society
- Genomics may change our lives through
- genetic determinism (will we have a false
impression of our future?) - nature versus nurture, nature and nurture, nature
over nurture, etc. - issues related to access to care
- confidentiality/privacy of information
- the right to know or not know, and not to act
- informed consent
- patenting and licensing
23What Can Health Care Professionals Do To Prepare
For Genomic Medicine?
- We need to learn to think genomically to
- realize how and when genomic factors play a role
in patient care - be able to explain genomic concepts as they
pertain to patient care - effectively use genomic screening (including
family history-taking) and testing - deal with genomic risk and predisposition
24What Can Health Care Professionals Do To Prepare
For Genomic Medicine?
- We need to learn to think genomically to
- realize the personal/family and societal impacts
of genomic information - protect genomic privacy
- use genomics to individualize patient care
- use genomics to promote health and prevent disease
25What Can Society Do To Prepare For Genomic
Medicine?
- We need to understand
- basic genomic concepts as they pertain to health,
health promotion and disease prevention - the uses of genomics in health care
- how to deal with genomics in health care
including the right to say no - the societal impacts of genomics and genomic
medicine--especially the ethical, social, legal,
political and financial issues
26Acknowledgment
- I would like to thank Alan Guttmacher, M.D.,
- Special Assistant to the Director, National
- Human Genome Research Institute, National
- Institutes of Health, Department of Health and
- Human Services, for his help in preparing this
- presentation.