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Interviews
Barney D. Gill
University of Washington School of Medicine
Department of Molecular Biotechnology
E-mail: bdgill@u.washington.edu
Exactly what is the nature of your research?
I
work along with a team of other researchers to find variations
in human genomic DNA. Collaborators of ours believe that
these variations may be important markers or indicators
of how susceptible one might be to having a genetic predisposition
to having heart disease (high blood pressure, hypertension,
etc.) SNP's, or single nucleotide polymorphisms, are the
"hot" area right now, and many researchers are
using these as markers. In the past, other types of markers
were used. Single nucleotide substitutions and unique
insertions/deletions are the most common form of DNA sequence
variation and disease causing mutation in the human genome.
I
am currently working on a project involving single-well
genotyping of diallelic sequence variation using a two
color ELISA oligonucleotide ligation assay. With this
assay, were are able to use 96 well plates to type 96
individuals at once, at one variation site. Through sequencing,
we were able to determine where these variations occurred
in the particular cardiovascular disease gene that we
were looking at. Then we construct an assay to look at
that particular variation. It is specific enough to where
if the polymorphism is a c/t for example, we can tell
by this plate what allele this individual has, or if they
have both! Using this colorimetric assay, if the well
turns red say, then they have one allele; if it turns
blue, they also have the other allele (heterozygote).
If only one color comes up, then they are homozygote at
that locus for the particular allele. This is a very convenient
assay for high-throughput genotyping. We do anywhere from
6-20 of these plates each day, so you can tell that this
generates a significant amount of data.
I
am currently looking into efficient automation of particular
parts of this assay, and ways to increase throughput and
decrease user handling error.
What do you find most exciting about your research?
I
think that finding new solutions to problems is the most
exciting part of this research; getting something to work
that hasn't in the past for whatever reason, figuring
out what the "problem" was. It is also nice
to see ideas about automation be implemented, and then
train fellow colleagues on its use.
What are you trying to accomplish?
By
having all of this data and information, our collaborators
(who are generally population geneticists) can hope to
find links between the likelihood of having cardiovascular
disease and the genetic variations.
Why is your research so important?
This
research has HUGE implications for the future cardiovascular
health of humans. Obviously there major issues to be worked
out, and the debate may never end, about genetic manipulation
and therapy. Knowledge is a good thing, and if you knew
that you were predispositioned to getting heart disease,
you could then adjust your lifestyle and diet accordingly
to do everything possible to ensure your longevity.
What have you discovered so far? Have you published your
findings?
We
have found lots of new single nucleotide polymorphisms
that were not known to exist before, and possibly laid
the groundwork to finding links to heart disease through
genetic variation. We also have a great team of programmers
here that have written new software (that tons of people
now use!) for analyzing DNA sequence data and ola data.
We
have many publications out, and they can be found at our
website http://droog.mbt.washington.edu.
What makes the University of Washington such a great genetics
research center?
Well,
I would have to say that there must have been a joint
"moving" of great minds to work together, and
that place happened to be Seattle. The ties that the UW
has to the Fred Hutchinson Cancer Research Center and
many biotechnology companies (most were started by UW
scientists, including Zymogenetics, Immunex, and ICOS
I believe) have made it world renowned. The Seattle area
is also becoming known as the hotbed for not only genetics,
but bioinformatics and programming as well. I have even
seen reports listing it "better" than the Silicon
Valley. Our department was started by a large funding
from Bill Gates (of Microsoft fame). He founded our department,
and his first step was to lure Lee Hood from the California
Institute of Technology to the UW. Lee Hood was already
world famous for developing the technology for the fluorescent
automated sequencer and other great innovations applicable
to the genetics field. He also had done some great genetics
research. Many great scientist followed him here, including
Debbie Nickerson, Ph.D., who I work for, and Barbara Trask,
Ph.D., who invented Fluorescent In Situ Hybridization
(FISH) I believe.
Have you done other types of research?
Prior
to this, I worked in the Botany department here at the
University of Washington. I worked on a brown, unicellular
algae called Heterosigma carterae. It is common in the
Pacific Northwest, and certain unknown environmental cues
cause it to "bloom." I am sure you are familiar
with a "red tide?" It is caused when a red algae
or dinoflagellates bloom near the coastline. They typically
consume considerable amounts of oxygen from the water,
choking off fish and other marine animals. Several blooms
in Puget Sound and up in British Columbia in the past
few years have cost fish farmers millions of dollars of
losses. I worked particularly on an enzyme that may trigger
the bloom, Phosphoribulokinase. I cultured the algae in
many different types of conditions, and looked at the
enzymes activity with a spectrophotometric assay.
What types of equipment do you use?
Automated
Sequencers, pipetting robots, synthesizers, HPLC for purifying
primers.
Why have you chosen this field?
Discovery
is very interesting, and there are many untouched areas
in this field presently. Another lure was the opportunity
to be in a "head of the field" (in terms of
technology) type of environment.
How did you get involved in researching? What steps did
you take to reach your position?
I
got involved in researching because I had questions in
my academic training that my professors could not answer.
I attended Kelso High School, and then received a B.Sc.
in Zoology from the University of Washington, with a heavy
emphasis on research.
What are your career goals?
Good
question. To be successful and happy.
What other types of genetic research is being conducted
at the university?
Anything
you can think of; name it. Forensics, genome studies,
population genetics, mapping, genetic analysis software
design, and on and on.
What advice do you give to high school students interested
in entering the field of genetic science?
Read
everyday, anything. Do well in high school. Take advanced
courses. Travel. Build yourself as a person, not just
a scientist. Take as much math and science as you possibly
can in high school. Study hard for the SAT. Have hobbies.
Find mentors.
Barney Gill
E-mail: bdgill@u.washington.edu

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