News Release

Whitehead Receives $35 Million Grant From National Human Genome Research Institute (NHGRI)

Peer-Reviewed Publication

Whitehead Institute for Biomedical Research

International Consortium Announces Successful Completion of Pilot Project; Accelerated Timetable for Large-scale Effort to Sequence the Human Genome

Cambridge, Massachusetts--The Whitehead Institute for Biomedical Medical Research will receive approximately $35 million from the National Human Genome Research Institute (NHGRI), National Institutes of Health, to participate in the first year of the definitive, full-scale effort to sequence the human genome.

An international consortium today announced successful completion of the pilot phase of sequencing the human genome and the start of the large-scale effort to read all 3 billion DNA letters (referred to as DNA bases) that make up the instruction book for a human being. Based on experience gained from the pilot project, the international consortium now predicts they will produce at least 90 percent of the human genome sequence in a "working draft" form by the spring of 2000, considerably earlier than expected.

The five major sequence producers in the international consortium will be three U.S. laboratories funded by NHGRI (the Whitehead Institute, Washington University School of Medicine in St. Louis, Missouri, and the Baylor College of Medicine in Houston, Texas); the Joint Genome Institute of the U.S. Department of Energy (DOE); and the Sanger Centre, supported in the United Kingdom by the Wellcome Trust. The NHGRI awards total $81.6 million; the Wellcome Trust has announced that they are adjusting the funding of the Sanger Centre to make available approximately US $77 million for human DNA sequencing over the next 12 months.

Dr. Eric S. Lander, director of the Whitehead/MIT Center for Genome Research, says, "In the pilot phase we and others designed and tested new technologies and strategies for scaling up DNA sequencing;the results were tremendously positive. We showed that we could generate highly accurate, continuous DNA sequence in a cost-effective manner. Now we're ready to move ahead."

During the pilot phase, eight scientific teams supported by NHGRI, DOE, and international collaborators completed the sequence of over 480 million bases, of which 260 million (or close to 10 percent of the human genome) are in high-quality finished form. The finished sequence produced by the pilot projects met or exceeded the international accuracy standard of no more than one error in 10,000 bases. In fact, the most recent assessment showed that leading sequencers are ten times more accurate than that, producing fewer than 10 errors for every million bases sequenced. Pilot project participants also drove down the cost of sequencing, from approximately $2 per base when the pilot project started to an average of 20 to 30 cents per base today. The consortium members expect to reduce the cost even further as the project progresses.

The consortium's goal is to produce a working draft covering at least 90 percent of human genome sequence within one year. In plans drawn up last fall, Genome Project leaders projected completing the working draft by December 2001. The new consortium goal advances this timetable by more than a year and a half. The working draft will then serve as the scaffold for the painstaking but critical work of finishing, which involves closing gaps and correcting errors, leading to completion of the final high-quality, continuous human DNA sequence by 2003 at the latest.

"This joint initiative marks a major expansion of the collaborative spirit of the international sequencing effort, with the goal of completing the sequence of the 3 billion bases of human DNA as soon as possible," said Dr. Francis S. Collins, director of the NHGRI. The international consortium has evolved into a tightly knit collaboration with weekly meetings, shared materials, and shared protocols. The NHGRI funded laboratories will be responsible for producing approximately 60 percent of working draft sequence. DOE's Joint Genome Institute and the Sanger Centre will be responsible for producing approximately 10 percent and 33 percent, respectively.

Dr. Lander says, "The consortium is committed to releasing all DNA sequence into DNA data bases within 24 hours and will not patent any of the sequence generated. Thus, the information will be available immediately to academic researchers answering critical questions about human disease through basic biomedical research, and to corporate scientists engaged in drug development to fight human disease."

Dr. Michael Morgan, chief executive of the Wellcome Trust Genome Campus, concurs: "Through this major publicly funded effort we can ensure that sequence data remains in the public domain for access by all researchers for the development of future healthcare treatments. This is crucial for the real medical benefits to be realized efficiently."

The sequencing effort is also designed so it can take advantage of any sequencing work done in the private sector. This may allow completion of the final sequence far sooner than 2003. "The Human Genome Project looks forward enthusiastically to cooperating with all parties that can contribute to more rapid public availability of the human genome sequence," said Dr. Collins.

Dr. Collins added that the three new awards to the Whitehead Institute, Washington University, and Baylor College of Medicine were based on a peer review process that evaluated the largest of the pilot projects, those that had completed 15 million bases of high-quality, finished sequence by December 1998. NHGRI will review additional applications in March and plans to award additional funds for large-scale human DNA sequence production in May.

"We are very proud to be part of this international effort," says Dr. Gerald R. Fink, director of the Whitehead Institute. "The complete human genome sequence will be the foundation for all biomedical research in the 21st century. Just a decade from now, our students will be unable to conceive of a time when researchers lacked this critical tool for advancing knowledge of human health and disease."

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