Project offers free mouse sequence
http://www.nature.com/cgi-taf/DynaPage.taf?file=/nature/journal/v407/n6805/full/407663b0_fs.html
Nature 407, 663 - 664 (2000) © Macmillan Publishers Ltd.
October 13, 2000
PAUL SMAGLIK AND ALISON ABBOTT
[PHILADELPHIA MUNICH] Researchers will get a free version of the mouse genome about two
years earlier than planned, thanks to a public-private
collaboration announced last week. A consortium
will pump $58 million into the project — enough to
sequence the organism three times over by April.
Celera Genomics, of Rockville, Maryland, will finish
its mouse project next month, but the information will
be available only to subscribers. In supporting the
public project, rather than paying to use Celera's
databases, the consortium's biggest pharmaceutical
sponsors, Merck and SmithKline Beecham, have
committed themselves to making what their
spokespersons call "precompetitive information"
freely available.
The companies have each given $6.5 million to the public effort. Other sponsors include
Affymetrix, the US National Institutes of Health and Britain's Wellcome Trust.
In announcing the consortium last week at a meeting of the American Society of Human
Genetics, Francis Collins, director of the National Human Genome Research Institute,
emphasized that the project is not competing with Celera, in contrast to the portrayal of their
sequencing efforts of the human genome. "This is not a race," he said.
The mouse sequence will make it easier to understand the human genome, as the two share
many genes — although not the repetitive stretches of 'junk' DNA that make up a significant
part of each.
The two mouse projects use different strategies. Celera is sequencing three different strains of
mouse once each, whereas the public effort is sequencing the common 'black six' strain three
times.
Celera's effort will allow subscribers to detect subtle differences between strains; the public
project will give a more complete view of one strain.
But Celera president Craig Venter sees duplication, not difference. The consortium's effort is a
"waste of public money", he says. "It would make more sense for scientists to pay for Celera
licences than to pay for the genome to be sequenced again."
Roger Schultz, assistant professor of human growth and development at the University of
Texas Southwestern Medical Center, sees merit in the public approach, which aims to
sequence both mouse and human genomes several times more than Celera intends.
"Personally, I'm more interested in the high-quality human product, although a good mouse
project can help you find highly conserved regions, and therefore genes," he says. The Texas
centre is one Celera's several academic subscribers.
Celera subscribers will get the first view of the mouse, as the company expects to finish
sequencing next month. If the public project finishes its first phase in March, as planned, the
data could be largely assembled by the end of next year. Plans announced by the Human
Genome Project last autumn called for a draft of the mouse by the end of 2003, to be fully
completed by the end of 2005.
The Whitehead Institute at the Massachusetts Institute of Technology, Washington University
in St Louis, and the British Sanger Centre near Cambridge will do the bulk of the public
project's shotgun sequencing. Washington University is halfway through building a map of the
mouse that will help in assembling a rough draft from the mouse shotgun data.
http://www.nhgri.nih.gov/NEWS/MouseGenes/mouse_release.html