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Gerald R. Fink, PhD
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Member, Whitehead Institute
Professor of Genetics, MIT
617.258.5215 phone
gfink@wi.mit.edu
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Whitehead Member Gerry Fink developed baker's yeast as a model for studying the fundamental biology of all organisms. Fink's creative use of classical genetics, biochemistry, and molecular biology has yielded numerous discoveries in biology. His lab has pioneered a better understanding of gene regulation, mutation, and recombination.
[
fink research 220 kbps QuickTime]
Selected Achievements
• Pioneered field of yeast molecular biology
• Developed a method for genetically engineering
salt and drought tolerant plants
• National Academy of Sciences/U.S. Steel
Foundation Award in Molecular Biology
• Awarded 2001 George W. Beadle Medal by the
Genetics Society of America
• Received first honorary doctorate awarded
by Cold Spring Harbor Laboratory
• Elected to American Philosophical Society,
the oldest U.S. society devoted to the advancement
of scientific and scholarly inquiry
• Awarded 2010 Gruber Genetics Prize |
Topping the list of Fink's seminal contributions to
the field was his development of a technique for "transforming"
yeast that allowed researchers to introduce a foreign
piece of DNA into yeast cells and study the inheritance
and expression of that DNA. This technique laid the
groundwork for the commercial use of yeast as biological
factories for manufacturing vaccines and other drugs
and set the stage for similar manipulations in more
complex organisms.
Fink's discovery of filamentation in yeast uncovered
a mechanism by which disease-causing fungi switch from
a benign to infectious form and invade human tissues.
The analysis of this switch provided the scientific
basis for the search for new antibiotics. More recently,
Fink used whole genome profiling to identify metabolic
pathways responsible for fungal virulence that do not
occur in humans and, thus, provide targets for drugs
that are specific to pathogenic fungi. He has also identified
a genetic mechanism by which pathogenic fungi can quickly
alter their outer coatings, or appearance, and thus
potentially evade the immune system.
Fink was instrumental in introducing Arabidopsis thaliana
as a model organism for studying plant development.
He identified a mechanism of hormone signaling and outlined
the key steps in the plant's response to gravity. Most
recently, he uncovered mutants that enable plants to
be grown in water as salty as seawater.
In 2003, Fink chaired the National Academy of Sciences
Committee on Research Standards and Practices to Prevent
the Destructive Use Application of Biotechnology. This
work provided the nation with critical guidance on how
to deal with the threat of bioterrorism without jeopardizing
scientific progress.
Fink is a Founding Member of the Whitehead Institute
and American Cancer Society Professor of Genetics at
MIT. He was director of the Whitehead from 1990 to 2001.
Fink received his PhD degree in genetics from Yale University
and served for 15 years on the faculty of Cornell University.
A past president of the Genetics Society of America,
he is a member of the National Academy of Sciences,
a fellow of the American Academy of Arts and Sciences,
and a member of the Institute of Medicine.
Selected Publications
Verstrepen, K.J., Jansen, A, Lewitter, F., Fink, G.R.
(2005) Intragenic tandem repeats generate functional
variability. Nature Genetics, 37, 986-990.
Fink, G.R. (2005). A transforming principle.
Cell. 120: 153-154.
Chen, H., Fujita, M., Feng, Q., Clardy, J., Fink, G.R.
(2004). Tyrosol is a quorum-sensing model in Candida
albicans. Proc Natl Acad Sci, USA 101: 5048-5052.
Verstrepen, K.J., Reynolds, T.B., Fink, G.R. (2004).
Origins of variation in the fungal cell surface.
Nat. Rev Microbiology 2: 533-540.
Liu, S., Milne, T.G., Kuremsky, J., Fink, G.R., Leppla,
Stephen H. (2004). Identification of the proteins
required for biosynthesis of diphthamide, the target
of bacterial ADP-ribosylating toxins on elongation factor-2.
Mol. Cell Bio. 24: 9487-9497.
Lorenz, M.C., Bender, J.A., Fink, G.R. (2004). The
transcriptional response of Candida albicans upon internalization
by macrophages. Eukaryotic Cell 3: 1076-1087.
[research summary]
[publications (pubmed database)] |
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