Tanya Lewis,
LiveScience Staff Writer
Date: 14 April
2013 Time: 02:00 PM ET
This month
marks the 10-year anniversary of the Human Genome Project, a 13-year
international effort to determine the sequence of the 3 billion
"letters" in a human being's DNA.
The $3 billion
project, led by the U.S. Department of Energy and the National Institutes ofHealth,
began in 1990 and was completed on April 14, 2003. In the decade since then,
scientists have achieved many important milestones in using genomic discoveries
to advance medical knowledge.
Sequencing
technology has vastly improved in recent years. Sequencing the first human genome cost
about $1 billion and took 13 years to complete; today it costs about $3,000 to
$5000 and takes just one to two days.
Probing genome
function
But just
knowing the sequence would be meaningless without a way to interpret it. So
researchers found ways to study the genome’s function, by sequencing the
genomes of 135 other organisms and surveying the global variation among human
genomes.
Researchers
compared the genome
sequences of other animals, such as chimpanzees and
platypuses, as well as other eurkaryotic organisms (those whose cells have a
nucleus), such as yeast and flat worms. From this comparison, scientists could
identify stretches of DNA that have remained largely unchanged over the course
of evolution. Five to 8 percent of the human genome has been unchanged for
thousands of years.
One of the
more surprising findings is how little of the human genome (only 1.5 percent)
actually encodes proteins, the molecular building blocks that perform most of
the critical functions inside cells.
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