|
1901 2012
Prize category:
|
The Nobel Prize in Physiology or Medicine 1993
Richard J. Roberts, Phillip A. Sharp
The Nobel Prize in Physiology or Medicine 1993
Nobel Prize Award Ceremony
Richard J. Roberts
Phillip A. Sharp
Phillip A. Sharp
Born: 6 June 1944, Falmouth, KY, USA
Affiliation at the time of the award: Massachusetts Institute of Technology (MIT), Center for Cancer Research, Cambridge, MA, USA
Prize motivation: "for their discoveries of split genes"

Autobiography
A sense of place was and remains an
important part of my life. I was born in a rural community in the
northern hill country of Kentucky. My earliest memories are those
of a child playing around the house on our family farm, located
in a bend of the Licking River near McKinneysburg. My mother,
Kathrin Colvin Sharp, had grown up in that same house and her
family had been part of this community for many generations. My
father, Joseph Walter Sharp, grew up nearby within walking
distance of the nearest town and county-seat, Falmouth. Both
parents came from large families and I was surrounded by
grandparents, aunts, uncles, siblings and cousins.
My formal education was entirely in the public schools of
Pendleton County: McKinneysburg Elementary, Butler Elementary and
High School and Pendleton County High School. Even though my
studies never interfered with sports or fun, I managed to gain an
appreciation of math and science.
All through my childhood, my parents strongly encouraged me to
attend college. With that in mind, they taught me to save my
money for college tuition, and, even more important, they allowed
me to earn it by raising cattle for the market and growing
tobacco. The rural background of my childhood made me feel more
comfortable attending a small institution in a familiar
environment. Therefore, I entered a small liberal arts school,
Union College, in the foothills of eastern Kentucky. Union is in
Barbourville, the county-seat of Knox County, and in those days
it was one of the gateways for the youth from the mountains in
the eastern part of the state to emerge into a larger world.
While at Union, I majored in chemistry and mathematics and
decided that I wanted to continue to study and learn about
science, particularly chemistry. I also met and married a lovely
girl from New Jersey, Ann Holcombe (Sharp).
A young professor at Union, Dr. Dan Foote, became a good friend
and encouraged me to apply to the Department of Chemistry at the
University of Illinois. This old and distinguished department
must have recognized some hidden promise as I was offered a
fellowship and soon began graduate studies under Victor
Bloomfield in physical chemistry. Victor was an excellent mentor
as he encouraged both my scientific as well as cultural growth.
He provided funds for my participation in national scientific
meetings and broadened my perspective on society and culture by
being a long-haired liberal, well-read and artistic friend.
Fortunately, I was deferred from the Vietnam draft for a number
of years and was able to finish graduate school. My thesis dealt
primarily with the description of DNA as a polymer using
statistical and physical theories. My attempts at experimental
science at this stage were juvenile. In spite of my youth on the
farm, I was never very skilled in manual tasks; in fact, I soon
lost interest in any complex "hands on" manipulations.
The 1966 volume of the Cold Spring Harbor Symposium on The
Genetic Code stimulated my interest in molecular biology and
genetics. A subsequent letter to Norman Davidson at the California Institute of
Technology resulted in an offer of a postdoctoral position in
1969 and my immersion into a vibrant research program in
molecular biology. Ron Davis, a graduate student in Norman's lab
at the time, had previously developed the heteroduplex method for
visualizing deletions in phage genomes with the electron
microscope. Jerome Vinograd in an adjacent laboratory had
discovered the superhelical structure of animal virus genomes. In
this environment, I began the transition to experimental
molecular biology by using the heteroduplex method and electron
microscopy to study the structure of plasmids of the sex factors
and drug resistant factors of bacteria. I was particularly
interested in how sex factor plasmids acquired genomic sequences
from the bacterial chromosome. We found that both sex and drug
resistance factors contained transposable elements. This
experience taught me many things, including the power of novel
methodology and how a simple experiment can transform the
understanding of an important problem.
At the end of my stay at Caltech, I opted to extend my
postdoctoral period and begin to study the structure and pathway
of expression of genes in human cells. The expression of genes of
animal viruses with DNA genomes was the only experimentally
approachable system at that time, and this led me to a further
postdoctoral year at Cold Spring Harbor Laboratory under the mentorship
of Jim Watson. Here, I entered a
close-knit scientific commune of extremely talented people who
lived and worked together in an isolated environment for nine
months, and then were immersed in a continuous scientific meeting
for the remaining three summer months.
At the Lab Joe Sambrook, a staff member, I, and others used
hybridization techniques to map sequences in the simian virus 40
genome that were expressed as stable RNAs in both infected cells
and oncogenic cells transformed by this virus. These were
important results for understanding the biology of this
papovavirus and helped move the laboratory into a very rapidly
advancing field of research - the molecular and cell biology of
tumor viruses. Luckily, or perhaps by design at a higher level,
Ulf Pettersson, an expert in the growth of human adenovirus who
had done graduate studies with Lennart Philipson in Uppsala,
Sweden, was a fellow postdoctoral associate and my office mate at
Cold Spring Harbor. Adenoviruses are common causes of respiratory
and other types of infections in man; however, when infected into
newborn rodents, they can cause tumors. The high levels of both
replication and viral protein expression made the growth cycle of
this virus ideal for the study of gene structure and regulation.
Furthermore, the then recent discovery of restriction
endonucleases offered the prospect of fragmenting the viral
genome of 35,000 base pairs into tractable units. Ulf, I, and
others generated the first restriction endonuclease maps of this
virus, and Dr. S. Jane Flint and I began to analyze the regions
of the genome expressed as mRNAs in both productively infected
cells and in adenovirus transformed cells. This was an exciting
period in the molecular biology of adenovirus with the
discoveries (a) that only one specific fragment of the genome,
the E1 region, was responsible for oncogenic transformation; (b)
that restriction endonuclease length polymorphism could be
utilized to generate genetic maps; (c) the mapping of specific
genes on the viral genome; and (d) generation of a viral map of
sequences expressed as stable RNAs.
Salvador Luria, the Director of
the then recently established Center for Cancer
Research at the Massachusetts Institute of Technology, called in
1974 to inquire if I would be interested in a position at the
Center. After a brief visit to MIT I accepted. Fortunately, I was
assigned laboratory space on the 5th floor, which was shared with
David Baltimore, Nancy Hopkins,
Robert Weinberg and David Housman. Salva
was a visionary who protected his young faculty from
unnecessary interruptions, thus allowing their research
programs to flourish in an ideal scientific environment. He
was also a role model for how a scientist could shape and lead
a community. That summer, Jane Flint moved with me to MIT and
we continued our analysis of adenovirus transcription,
focusing on quantitating the levels of RNA from all parts of
the genome in the nuclear and cytoplasmic compartments of the
cell. We found that the nuclei of cells productively infected
by adenovirus contained abundant sets of viral RNAs which were
not transported to the cytoplasm. We speculated that these
long nuclear RNAs were processed to generate the cytoplasmic
mRNAs. This stimulated our interest in comparing the relative
structures of nuclear precursor RNA and cytoplasmic mRNA from
the adenovirus genome. We were joined in the latter part of
these studies by a postdoctoral fellow, Dr. Susan Berget. For
Sue, these studies were the beginning of a much more
interesting series of experiments which form the first part of
the lecture.
As mentioned above, Ann and I were married in 1964 while still
undergraduates at Union College. Our three daughters arrived on a
schedule which approximated a seven year itch: Christine Alynn
was born in 1968, while I was still in graduate school, Sarah
Katherin was born in 1974, just before we moved to New England,
and Helena Holcombe was born in 1981. Ann teaches a preschool
class in Newton, Massachusetts, the town we have made our home
since moving from Cold Spring Harbor. My family and are deeply
enamored with New England. We enjoy its rural towns, coastal
beauty, and the changes of seasons.
Through the years at MIT my environment has remained relatively
constant, though changes have occurred. David Baltimore and
Robert Weinberg left the Center in 1983 to found the Whitehead Institute,
which is associated with MIT. Salva retired from MIT in 1985 and
I assumed his position as Director of the Center for Cancer
Research. In 1991, I relinquished the Directorship to Richard
Hynes and became the Head of the Department of Biology. The
development of biotechnology has both enriched and complicated my
work. Walter
Gilbert of Harvard and I, along with a number of European
colleagues, founded the biotechnology company Biogen in 1978 in
Geneva, Switzerland. This organization and the friends who have
worked for it have remained an important part of my life
since.
My collaborators over the years have been: (listed in
alphabetical order) A. S. Baldwin, S. M. Berget, A. J. Berk, K.
Berkner, B. Blencowe, M. A. Brown, S. Buratowski, C. Carr, R. W.
Carthew, C. Cepko, D. Chang, D. Chasman, L. A. Chodosh, G. Chu,
R. G. Clerc, J. D. Crispino, D. J. Donoghue, A. Z. Fire, D. E.
Fisher, S. J. Flint, M. Garcia-Blanco, A. Gil, S. Gilbert, P. J.
Grabowski, H. Handa, U. Hansen, S. Hardy, S. Harper, T. Harrison,
M. Horowitz, P. S. Jat, R. Kaufman, J. Kim, R. Kingston, J.
Kjems, T. Kobayashi, M. M. Konarska, T. Kristie, A. I. Lamond, F.
Laski, J. LeBowitz, K. LeClair, F. Lee, I. Lemischka, A. M.
MacMillan, R. Marciniak, P. McCaw, R. Meyers, C. Moore, M. Moore,
M. Morton, M. Murata, R. Padgett, J. Parvin, J. L. Pomerantz, C.
Query, M. E. Samuels, J. Sedivy, S. Seiler, B. Shykind, H. Singh,
H. Skolnik-David, M. Timmers, A. Virtanen, J. Weinberger, and Q.
Zhou.
In 1980, Dr. Sharp received both the Eli
Lilly Award in molecular biology and the U.S. Steel Award from
the National Academy of Sciences. His awards are too numerous to
list but some include MIT's James R. Killian, Jr., Faculty
Achievement Award (1993), the John D. MacArthur Professorship
(1987-1992), the first Salvador E. Luria Professorship (1992-),
the New York Academy of Sciences Award in Biological and Medical
Sciences, the General Motors Research Foundation Alfred P. Sloan,
Jr., Prize for Cancer Research, the 1988 Louisa Gross Horwitz
Prize, the 1988 Albert Lasker Basic Medical Research Award, the
1986 Gairdner Foundation International Award, Canada, and the
1980 Dickson Prize from the University of Pittsburgh. In 1985, he
was the Harvey Society Lecturer and on May 4, 1991, he received
the honorary degree of Doctor of Humane Letters from Union
College, his Alma Mater. He is a member of the National Academy
of Sciences, the American Academy of Arts and Sciences, associate
member of the European Molecular Biology Organization and Fellow
of the American Academy for the Advancement of Science, the
American Philosophical Society, the Institute of Medicine of the
National Academy of Sciences, and a member of the editorial board
of the journal Cell. He is co-founder and Chairman of the
Scientific Board of Biogen, Inc., and member of its Board of
Directors.
Dr. Sharp has a distinguished record of public service, which
partially includes having served as a member of the President's
Advisory Council on Science and Technology, as co-chairman of the
Director of NIH's Strategic Plan, as a member of the Committee on
Science, Engineering, and Public Policy (COSEPUP), as a member of
the Search Committee of Director, National Center for Human
Genome Research, and more recently, as a member of the Search
Committee for the Director, Office of AIDS Research, NIH. His
career publications in peer reviewed and other journals are over
255.
From Les Prix Nobel. The Nobel Prizes 1993, Editor Tore Frängsmyr, [Nobel Foundation], Stockholm, 1994
This autobiography/biography was written at the time of the award and later published in the book series Les Prix Nobel/Nobel Lectures. The information is sometimes updated with an addendum submitted by the Laureate.
Copyright © The Nobel Foundation 1993
MLA style: "Phillip A. Sharp - Autobiography". Nobelprize.org. 21 May 2013 http://www.nobelprize.org/nobel_prizes/medicine/laureates/1993/sharp.html
