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Human Cloning May Be Impossible
Excerpt by
Lauran Neergaard, AP Medical Writer
WASHINGTON - Cloning humans,
or any other primates, may be impossible with today's techniques
because of a fundamental molecular obstacle, say scientists trying
to understand why attempts to clone monkeys have failed.
From the very first step, cloned
primate cells don't divide properly, causing a helter-skelter
mix of chromosomes too abnormal for pregnancy to even begin, University
of Pittsburgh researchers reported Thursday in the journal Science.
"Most people in the cloning field
will be surprised by this," said lead researcher Gerald Schatten.
"This work demonstrates there's a pothole in the process. We now
know the depth and breadth of the pothole, and we're designing
strategies to get around" it.
Dozens of animal clones
including cows, pigs, mice, goats and a cat have been born
since Dolly the sheep became the first new being created from
an adult cell in 1997. But it's still a very uncertain field:
Many are stillborn and some survive only with severe defects.
A cult group claimed in December
to have cloned a person, something never verified. A doctor who
separately is pursuing human cloning has reported in an Internet
journal preliminary data on an early-stage cloned human embryo,
but with no chromosome information.
Cloning experts worry that attempting
human cloning is dangerous not just because of all the barnyard
clones with birth defects, but because attempts to clone monkeys
far closer genetically to people using the Dolly
technique so far have failed.
To clone, scientists harvest an
unfertilized egg from a female donor, removing the genetic material
and replacing it with new DNA from an adult cell of the animal
to be cloned. An electric shock coaxes it into dividing. If all
goes well, the egg grows into an embryo that can be implanted
into a surrogate mother.
It took 277 attempts before Dolly
was born. Schatten's group tried even longer to clone a rhesus
monkey 724 eggs that yielded only 33 embryos and not a
single pregnancy.
For cells to properly divide, chromosomes
must duplicate themselves and precisely line up along a zipper-like
structure called a spindle. Once the chromosomes are in place,
the spindle helps the cell pull apart into two. During human reproduction,
if the chromosomes don't split properly, defects such as Down
syndrome result, or the pregnancy fails.
Schatten wondered if chromosome
abnormalities were behind failed monkey clonings. Indeed, inside
cloned monkey cells, the Pittsburgh researchers discovered deformed
spindles and chaotic chromosome numbers.
Why? Eggs harbor proteins that
act as molecular motors that are key to spindle formation. In
primates, those proteins are so tightly bound to the egg's DNA
that cloning's first step of DNA removal pulls them out, too,
dooming hope of later pregnancy, Schatten said.
In other mammals, enough spindle-forming
proteins float in the egg's remaining fluid for reproduction to
occur, he said.
The discovery is very important,
said Dr. Duane Kraemer, a successful cloner of non-primates at
Texas A&M University.
"The fact that they don't get pregnancies
at all is suggestive that there is something different going on
there than with other species," he said. "It points to a potential
problem that may have to be solved before the next advance can
be made."
It's not just bad news for reproductive
cloning. It also means the related field of therapeutic cloning
using embryonic stem cells to grow customized tissues for
medical treatment may prove harder, too, Schatten said.
However, if 95 percent of cells growing in a lab dish have abnormal
chromosomes, the remaining good 5 percent could still be used,
he added.
His lab is exploring a way to overcome
the problem, by combining cloning with old-fashioned egg fertilization.
The sperm-and-egg joining jump-starts spindle formation. Schatten
then pulls out that sperm and egg DNA, leaving just the clone
DNA in the now-growing monkey cells.
"The value of this for deriving
embryonic stem cells is going to be very attractive," Schatten
said.
Reference
Source 102
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