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Who owns your genes?

by Jeffrey P. Kahn, Ph.D., M.P.H.
Director, Center for Bioethics
University of Minnesota

March 21, 2000
Web posted at: 9:25 a.m. EST (1425 GMT)

In this story:

Three billion base pairs, but what do they mean?

Patenting the meaning of genes

Teaching an old system new tricks


Last week, President Bill Clinton and Prime Minister Tony Blair announced that their governments would work together to make the fruits of the Human Genome Project publicly available. Much reporting of the announcement suggested that it signaled a challenge to patent claims by researchers, universities and biotech companies. The reaction was shared by investors, as stock prices for these companies fell sharply. But what does the announcement change, if anything, and what are the fundamental issues with the ownership of genetic information?

Center for Bioethics

What's your opinion?

Three billion base pairs, but what do they mean?

The Human Genome Project is producing the first complete list of the genetic code for humans. That list is a string of about 3 billion base pairs of DNA -- the chemical that makes up our genes.

But the list being produced is just the beginning of our understanding of the human genome, with the most important steps yet to come. What do the strings of base pairs code for, what does their product do in the human body and how do changes in the correct code affect human health?

Researchers and biotech companies are working to answer these questions, and their work requires access to the complete genetic code. So the code itself is a tool in research rather than its endpoint, and the Clinton-Blair announcement underscored the need to preserve free access to this basic information.

In fact the announcement doesn't do much to change the state of affairs. There are parallel efforts to sequence the entire human genome, one public and the other private. The public effort, funded largely by NIH as part of an international consortium, puts huge amounts of new genome information on the web on a daily basis. The private sector competition (an American company called Celera) produces genome information at about the same pace, but sells access to its database, licensing users who pay a fee.

Genome information is already effectively a public good, since anyone can access the public database on the web. What Celera offers users is a more sophisticated tool by which to manipulate and search. But it should be the same genomic information available to the public-genomic information that is not protected by any patent.

Patenting the meaning of genes

But using this basic information about the genome, scientists have begun to unravel what our genes mean -- predicting increased risk of disease or coding for characteristics such as personality. And the companies and institutions that pay these scientists have begun to successfully protect their efforts with patents.

The system of patents exists to protect the interests of both inventors and society. Inventors have the incentive of a limited monopoly on their innovations, allowing them to sell or license their products or techniques for profit. Society benefits by the advancements of innovation and the full disclosure of whatever has been patented.

But our system doesn't allow a patent for the discovery of a law of nature. Gravity couldn't be patented by Sir Isaac Newton -- even if he was the first to describe it. Mapping the raw sequence of a gene is viewed much the same way, unless a scientist can show the function of a particular sequence, such as in causing a disease such as cystic fibrosis. Such a gene would have obvious uses such as developing tests or treatment for the disease.

Even with this limitation on patent claims, the U.S. Patent Office has granted protection for a number of incomplete gene sequences, and apparently has many more applications pending. The Clinton-Blair announcement does nothing to address this issue.

Teaching an old system new tricks

Our 200-year-old patent system never was intended to address the question of patent protection for genes, and the slowly changing system coupled with rapidly changing science makes for strained public policy. This issue is becoming increasingly important, not only in this country but worldwide as genetic sciences increasingly become a global effort with a global market.

The challenge will be to protect the rights of the innovators while preserving the public nature of the information they use. A patent system creates rather than recognizes such rights, and we make bad policy when we forget the difference.

For the message board: Last week, President Bill Clinton and Prime Minister Tony Blair announced that their governments would work together to make the fruits of the Human Genome Project publicly available. Basic genome information is already public, but scientists, universities, and biotech companies are patenting information about how genetic information affects our health. Should anyone own genes and genetic information, or should it be a public resource? What are the implications of ownership versus free access to genetic information?

Post your opinion here.

Visit the
"Ethics Matters" Archive
where you'll find other columns from Jeffrey Kahn
on a wide range of bioethics topics.

"Ethics Matters" is a biweekly feature from the
Center for Bioethics and CNN Interactive.

Your Health: Implications of the Human Genome Project
March 17, 2000
U.S., Britain urge free access to human genome data
March 14, 2000
British firm applies for patent on gene profile system
March 8, 2000

National Human Genome Research Institute (NHGRI)
The Human Genome Project
UK Human Genome Mapping Project Resource Centre
Human Genome Project Information
The Human Genome Organisation (HUGO)

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