Scientists map human genome
Less than three years after they finished a working draft of the three billion letters of human DNA, scientists said their map was finished to 99.9 per cent accuracy - two years ahead of schedule. Experts said the sequencing would lead to new drugs, better forecasts of people's health and new ways to treat or prevent many of the most devastating human illnesses.Updated: Apr 15, 2003 19:18 IST
The book of genetic instructions for the human body is complete to an accuracy of 99.99 per cent, a scientific achievement once deemed impossible but now considered the foundation for a new era of medical advances, an international research team said.
With the entire sequence in hand and available to scientists worldwide, experts predicted it would lead to new drugs, better forecasts of people's health and new ways to treat or prevent many of the most devastating human illnesses.
A joint statement on Monday from the leaders of the six nations, including President George W Bush, said the genetic map "provides us with the fundamental platform for understanding ourselves from which revolutionary progress will be made in biomedical sciences and in the health and welfare of humankind."
The other five countries involved are France, Britain, Germany, Japan and China.
The group, along with a competing private effort, completed a rough draft of the genome in 2000, but that draft included thousands of gaps in the long sequence of DNA base pairs. Now all but 400 of those gaps have been closed.
"After three billion years of evolution ... we have before us the instructions set that carries each of us from a one-celled egg through adulthood to the grave," said Dr. Robert Waterston of the International Human Genome Sequencing Consortium. "It is written in an arcane language and encompasses a complexity that we just beginning to understand."
The genome is composed of about three billion pairs of DNA chemicals within 24 chromosomes. The genes that control the body's development, growth, functions and aging are made of specific sequences of these chemical pairs. A small change in these sequences can be enough to cause disease.
By identifying the correct and healthy sequence of base pairs, researchers hope to be able to find the disease-causing genetic flaws that could yield to treatment.
Scientists are still uncertain how many genes there are in the genome, but most believe it is about 30,000. This number is expected to be refined with more research.
Hundreds of scientists in the consortium, representing 18 organizations in six countries, started the sequencing work in 1990. American agencies and universities, led by the National Human Genome Research Institute and the Department of Energy, completed the project at a cost of about $2.7 billion, some $300 million less and two years earlier than the original estimate. The U.S. did about half of the DNA sequencing, and some of the money budgeted for the human project was spent on sequencing other organisms, such as the mouse, and on associated technologies.
Celeria Genomics, a private company, raced the international effort to produce a parallel rough draft of the genome. Completion of the competing efforts was announced at a joint news conference at the White House in June 2000. But Dr Francis Collins, director of the NHGR, said that Celeria did not go on to refine the rough draft, leaving the consortium with the only essentially complete sequence. Celeria leader Craig Venter now works for the Department of Energy.
Announcement of the completed sequence comes just days before the 50th anniversary of the discovery of the double helix structure of DNA by James Watson, an American, and Francis Crick, a British biophysicist. They shared the Nobel Prize for the work. Watson, who was the first director of the American sequencing effort, said at Monday's news conference that his decision to devote 3 per cent of the genome research effort to studying the ethical consequences of the gene sequencing may have been "the wisest decision that I made."
He said there were concerns that if the research identified people with a genetic predisposition for disease it could lead to discrimination in employment and in other elements of life. Forty states have now passed laws forbidding genetic discrimination and federal laws have been proposed.
Dr Francis Collins, head of the National Human Genome Research Institute, said the complete sequence of the genome is just the beginning of the genetic revolution. Researchers now will use the sequences to try to speed identification of genes that cause cancer, diabetes, heart disease and other disorders and then to develop drugs that either prevent or treat the disorders. Some disorders might be treated by manipulating or replacing flawed genes, he said.
First Published: Apr 15, 2003 19:18 IST