Excerpt from washingtonpost.com
In
March, a rumor surfaced in the scientific community that was
intriguing, and perhaps a bit chilling: According to those in the know,
researchers in China had successfully edited the genomes of human
embryos, altering their DNA in a way never accomplished in our own
species. MIT Technology Review reported on the murmurings
that someone had altered the germ line — the genetic information that
come together and form something new when eggs and sperm collide. Even
unconfirmed, those rumors led to a lot of debate about the potential
downsides of altering the germ line.
But it turns out the rumors are true.
On Wednesday, Nature News reported that the paper in question had been quietly published in a low-profile journal called Protein & Cell.
But no, you can’t expect to see any genetically altered humans running around in the coming months, for better or for worse. From MIT Technology Review:
The
team did not try to establish a pregnancy and say for ethical reasons
they did their tests only in embryos that were abnormal.
“These authors did a very good job pointing out the challenges,” says Dieter Egli,
a researcher at the New York Stem Cell Foundation in Manhattan. “They
say themselves this type of technology is not ready for any kind of
application.”
The work, led by Junjiu Huang of Sun
Yat-sen University in Guangzhou, focused on modifying the gene
responsible for β-thalassaemia, a blood disorder that can be fatal. They
used CRISPR, a cutting-edge gene editing tool that’s already made
serious waves in the genome editing of other species. By going after
genes at the earliest stage of human development — in a single-celled
embryo — theoretically one can make sure all the subsequent copies of
the gene are the superior version.
But we have a long way to go before that’s actually the case. From Nature News:
The
team injected 86 embryos and then waited 48 hours, enough time for the
CRISPR/Cas9 system and the molecules that replace the missing DNA to act
— and for the embryos to grow to about eight cells each. Of the 71
embryos that survived, 54 were genetically tested. This revealed that
just 28 were successfully spliced, and that only a fraction of those
contained the replacement genetic material. “If you want to do it in
normal embryos, you need to be close to 100%,” Huang says. “That’s why
we stopped. We still think it’s too immature.”
Indeed,
not all of the embryos that successfully received the new gene had it
throughout all of their cells. Many were mosaics, with some good copies
of the gene and some bad ones. Carl Zimmer points out
that this could end really badly: If a doctor tested the potential
embryos of a couple looking to edit out a deadly gene mutation, they
might take a cell sample that showed the embryo as having the healthy
gene. If it was a mosaic, the resulting baby might in fact have enough
copies of the bad gene to cause problems.
And in some of the embryos, the gene editing caused unintended mutations in other genes.
“I
believe this is the first report of CRISPR/Cas9 applied to human
pre-implantation embryos and as such the study is a landmark, as well as
a cautionary tale,” George Daley, a stem-cell biologist at Harvard
Medical School, told Nature.
“Their study should be a stern warning to any practitioner who thinks
the technology is ready for testing to eradicate disease genes.”
So
it’s an exciting first step, but nothing more. Science has a long way
to go before this is something we can do on embryos intended for
implantation, and some are already trying to discourage researchers from
taking the next steps toward that goal. Even the study authors
themselves are incredibly cautious about their findings, firmly
reporting that the technique is far from ready.
But you can be sure that such a caveat won’t stop a lot of hoopla about the pros and cons of “designer babies.”
Source Article from http://feedproxy.google.com/~r/AscensionEarth2012/~3/jwWKTIfypk0/the-rumors-were-true-scientists-edited.html
The rumors were true: Scientists edited the genomes of human embryos for the first time
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