Early
genetics discovery wins Cohen the Albany Prize
Largest medical award after Nobel shared with
colleague
By AMY ADAMS
Research laying the groundwork for modern genetic engineering has earned
Stanley Cohen, MD, the Kwoh-Ting Li Professor at the School of Medicine,
the 2004 Albany Medical Center Prize in Medicine, the largest medical
award after the Nobel Prize.
The annual $500,000 prize is the result of a $50-million gift by New York
City philanthropist Morris "Marty" Silverman to encourage and
recognize extraordinary and sustained contributions to improving health
care and promoting biomedical research with translational benefits applied
to improved patient care. Cohen shares the prize with Herbert Boyer, PhD,
co-author on his breakthrough 1973 paper, a founder of Genentech and professor
emeritus at UC-San Francisco.

Stanley Cohen
Cohen and Boyer are the fourth recipients of the prize. They appeared
at an award ceremony and press conference in Albany, N.Y., on April 23.
The pair's discovery allowed researchers to transfer pieces
of DNA between organisms, a process also called DNA cloning, opening the
door to the modern field of genetic engineering. Among the many lifesaving
discoveries developed using DNA cloning are insulin to regulate blood
sugar in diabetics, a clot-dissolving agent for stroke and heart attack
victims, a human growth hormone for underdeveloped children and interferon
for cancer patients.
"The world owes an infinite debt of gratitude to Drs. Cohen and Boyer
for their seminal research, which serves as the basis for today's biomedical
sciences and biotechnology industries," said James J. Barba, chairman
of the board, president and chief executive officer of Albany Medical
Center, who also chairs the national selection committee for the prize.
"Prior to their groundbreaking work, the scientific community was
uncertain whether genes could be isolated and transplanted into a foreign
host where they could survive and replicate. Their collaborative discovery
has spawned a multitude of treatments and diagnostic therapies for some
of mankind's most pernicious diseases."
Cohen and Boyer began their collaboration at a meeting in Hawaii in 1972.
Cohen had been working with circular pieces of DNA called plasmids, which
sometimes contain genes that make bacteria resistant to antibiotics. He
had learned how to transfer these plasmids -- and their antibiotic-resistant
genes -- between bacteria, but wanted to modify the plasmids to learn
more about how those genes functioned.
At the Hawaii conference Boyer described a new method of cutting DNA such
that the broken ends were genetically sticky and could easily reattach.
This method, involving a DNA-cutting enzyme called EcoRI, snipped
the DNA at very precise locations. Cohen and Boyer thought that by cutting
plasmids and other DNA with EcoRI, the pieces might stick together
in novel configurations.
"Although the concept seemed straightforward, no one knew at the
time whether novel plasmids constructed in this way would be capable of
being propagated in living cells," Cohen said.
In studies back at their respective Stanford and UCSF labs, Cohen, Boyer
and their colleagues Annie Chang and Robert Helling used this method to
snip a gene for antibiotic resistance out of one plasmid and place it
in a different plasmid. They put the reconfigured plasmid into E.
coli and those bacteria became resistant to the antibiotic. Bacteria
passed this plasmid to their offspring, conferring antibiotic resistance
to future generations.
This novel way of swapping DNA between E. coli was the basis
for the 1973 paper in the Proceedings of the National Academy of Sciences
and a Stanford/UCSF patent, which has now been licensed to more than 400
companies.
After achieving success in propagating new combinations of genes between
E. coli strains, the researchers tested whether genes could be swapped
between different organisms. Cohen and Chang transferred a gene from the
bacteria Staphyloccus aureus into E. coli. Although
the two bacteria are biologically quite different, E. coli replicated
the S. aureus gene and produced the functional protein. Later
experiments by Cohen, Boyer and their colleagues showed that even animal
genes inserted into a plasmid could make normal proteins in E. coli.
From these experiments the modern field of genetic engineering was born.
Gene cloning is now used in biology labs around the world to make crops
hardier, create new drugs and better understand disabling diseases.

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