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It took a leap of faith for Tian Xu to move from
Shanghai to Harlem in 1983, but he says the biggest
risk he has taken during his career was switching a
decade ago from fruit flies to mice as model organisms
to study gene functions.
Xu had made his name at
Yale and later as a postdoc at HHMI Vice President
Gerald M. (Gerry) Rubin's lab at the University of
California, Berkeley, for his Drosophila research—
conducting large-scale analyses of mutant flies to
decipher the roles of key genes and the biochemical
pathways related to cancer cell growth and metastasis.
But when Xu applied for an HHMI investigator
position in 1996, he made a bold proposal: he would
discover a way to create mutant mouse strains as easily
as developing mutant flies. That would represent a
big step forward in genetic screening of mice, about
99 percent of whose genes have direct equivalents in
the human genome.
“It was risky because I had a lot
to learn about mouse genetics,” Xu recalls, describing
the years of complex and often frustrating research that
it took for him to come up with the deceptively simple
breakthrough: using a moth transposon (“jumping
gene”) called piggyBac. Inserted into the mouse
genome, the tiny segment of DNA causes random
mutations when the animal breeds, disabling one gene per mouse and creating an efficient way to create
knockout mutants.
“Geneticists had been searching
for decades to find a system like this for mammals—an
efficient tool for transgenesis and mutagenesis,” says Xu,
who displays a framed cover of the August 2005 issue of
the journal Cell that featured his piggyBac report. “Now
we have the tool and we need to produce the mutant
mice strains for scientists to use in their research.”
With the new technique, scientists can produce
the mutant mouse strains about 100 times faster and
cheaper than they could with previous methods. And
Xu says the Institute of Developmental Biology and
Molecular Medicine at Fudan University in Shanghai,
which he coestablished at the urging of Chinese
officials, is able to produce such strains at a lower cost
than a similar facility in the United States.
At the Fudan institute, which already houses 25,000 mouse
cages, Xu and his researchers so far have produced
about 5,000 strains of knockout mice. The goal is to
produce 100,000 mutant strains by the end of 2010,
among which scientists hope to eventually identify
knockout equivalents for nearly all of the 25,000 or so
genes in the mouse genome.
“I wanted to accomplish
things with a real impact on society,” says Xu. “To do
that, you need to take some risks along the way.”—R.K.
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