Public, Private Sectors Join In Mouse Consortium

ing Results will Spur Discovery of Human Genesare less than 50% identical. When comparing the
and Their Functionssame DNA regions from human and mouse,
In October, a collaboration was announced totherefore, functional elements stand out clearly
speed up sequencing of the mouse genome andbecause of greater similarity.
produce a draft map by spring 2001. The MouseData from this project will be invaluable to us in
Sequencing Consortium (MSC) consists of six NIHannotating the final draft of the human genome,
institutes, the Wellcome Trust philanthropy, andobserved researcher John McPherson (Washington
three private companies. It provides anotherUniversity). It is exciting that we are moving
example of public and private sectors joiningrapidly toward completion of both projects, he
forces to support large-scale genomics researchsaid.
and generate freely available data crucial for basicRapid Data Release
biomedical research.The consortium project focuses on the black six
MSC members and their contributions are(C57Black/6) mouse strain, which is different
SmithKline Beecham ($6.5 million), the Merckfrom the three strains being sequenced by Celera
Genome Research Institute ($6.5 million),Genomics. Celera's data are available by paid
Affymetrix, Inc. ($3.5 million), Wellcome Trustsubscription.
($7.75 million), and NIH ($34 million). Total fundingThe MSC data-release policy calls for raw data
of $58 million will support sequencing for 6 months(individual DNA sequence traces, about 500 bases
at three centers: Whitehead Institute (Cambridge),long) taken directly from automated instruments
Washington University (St. Louis), and the Sangerto be deposited in two public databases. These
Centre in the United Kingdom.are operated by the National Center for
Why the Mouse?Biotechnology Information and the European
With the working draft sequence of the humanBioinformatics Institute. Individual sequences will be
genome in hand, scientists in industry andassembled into larger units as soon as a working
academia now seek to interpret its meaning. Thedraft is obtained.
mouse genomic sequence is a powerfulSequencing Strategy
comparative tool because genes in the twoMSC sequencing melds the best features of two
organisms are very similar. Understanding genestrategies used to produce a working draft of the
function in the mouse will accelerate knowledgehuman genome: the map-based shotgun method
about comparable human genes and will aid inused by the public Human Genome Project
understanding human disease and in developingconsortium and the whole-genome shotgun
new treatments.system used by Celera. The overall depth of
On average, protein-coding regions in the mousecoverage for the mouse genome will be 2.5x to
and human genomes are 85% identical. These3x, a level of detail useful to researchers; a
regions are evolutionarily conserved because theyfinished, highly accurate sequence is expected at
are required for biological functions shared by botha later date.
organisms. In contrast, noncoding genomic regions