MOUSE DNA TO AID BIOMEDICAL RESEARCH

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U.S. Department of Health and Human Services 
NATIONAL INSTITUTES OF HEALTH 
NIH News 
National Institute of Environmental Health Sciences (NIEHS)
<http://www.niehs.nih.gov/>

FOR IMMEDIATE RELEASE: Wednesday, October 25, 2006

CONTACT: Robin Mackar, 919-541-0073, <rmackar@xxxxxxxxxxxxx>

MOUSE DNA TO AID BIOMEDICAL RESEARCH

Researchers announced today that they have successfully resequenced the
DNA of 15 mouse strains most commonly used in biomedical research.  More
than 8.3 million single nucleotide polymorphisms (SNPs) were discovered
among the genomes of the 15 mouse strains and the data are now publicly
available.  These new data will help researchers better understand
complex genetic traits, such as why some individuals are more
susceptible to certain diseases, and will serve as a valuable resource
in determining how environmental agents influence the development of
disease.  

Single Nucleotide Polymorphisms, or SNPs (known as "snips"), are single
genetic changes, or variations, that can occur within a DNA sequence.
Because mice and humans share many of the same fundamental biological
and behavioral processes, including gene functions, these data will help
researchers understand human genetic susceptibility to almost 200
diseases such as Parkinson's, cancer, diabetes, heart and lung diseases,
reproductive diseases, and asthma and other childhood diseases, which
are affected by exposure to environmental substances. 

"Making this wealth of data freely available to the research community
is a significant milestone," said David A. Schwartz. M.D., director of
the National Institute of Environmental Health Sciences (NIEHS), part of
the National Institutes of Health, which funded the research.  "Each
mouse strain is genetically unique. Now that we know the DNA variations
for these mouse strains, we can compare the genetic makeup of one strain
that acquires a certain disease to another strain that does not get the
same disease.  In this way researchers gain insight into the same
processes that may cause one human to get a disease while another human
in the same environment remains disease-free."

The "Resequencing and SNP Discovery Project" began less than two years
ago through a contract between the National Toxicology Program at NIEHS
and Perlegen Sciences, Inc. of Mountain View CA.  Perlegen scientists
conducted the project using as a standard reference the 2003 DNA
sequencing of the C57BL/6J mouse strain -- the very first mouse strain
to undergo DNA sequencing.  The mouse models included in the
resequencing project are:  129S1/SvImJ, A/J, AKR/J, BALB/cByJ, BTBR T+
tf/J, C3H/HeJ, CAST/EiJ, DBA/2J, FVB/NJ, MOLF/EiJ, KK/HlJ, NOD/LtJ,
NZW/LacJ, PWD/PhJ, and WSB/EiJ. The 15 mouse strains were carefully
chosen because of their routine use as research models and their genetic
diversity.  The project used the same high-density oligonucleotide array
technology that was used to discover common DNA variation in the human
genome.

"Perlegen Sciences was excited to perform this scientific work, because
it promised to provide an extremely valuable resource. We believe the
data will generate a lot of knowledge about complex genetic traits,"
said Kelly Frazer, Vice President of Genomics at Perlegen Sciences, Inc.

"This project was highly anticipated by scientists. Now, we can go to
our  computer, click on the mouse strain we want to use, see the
sequence variations for that strain and compare it to the others," said
David Threadgill, Ph.D., an expert in mouse models of disease at the
University of North Carolina, Chapel Hill. "If we use multiple strains,
we can then look at the data after the animals are exposed to an
environmental substance and compare the genetic differences between the
strains that acquired a disease and those that did not. This will help
us begin to identify causes of differential susceptibility to disease."

"These mouse data will aid in our understanding of 'counterpart' genes
in humans, the corresponding molecular and biological pathways the lead
to disease susceptibility, and the environmental agents that trigger the
development of disease in susceptible people," said David Christiani,
M.D., Professor of Medicine at Harvard Medical School and Professor of
Occupational Medicine and Epidemiology at Harvard School of Public
Health. "The data will also be a great resource for pharmaceutical
companies that are developing new treatments for disease."

The data are available on the National Center for Biotechnology
Information website at <http://www.ncbi.nlm.nih.gov/SNP/>.  The NIEHS
Resequencing and SNP Discovery Project is overseen by the Institute's
Center for Rodent Genetics, which helps to facilitate interactions among
scientists working on mouse models of human disease and provides them
with the resources and information necessary to conduct their research.
For more information on the Center for Rodent Genetics, visit
<http://www.niehs.nih.gov/crg/home.htm>.  

The National Institute of Environmental Health Sciences (NIEHS), a
component of the National Institutes of Health, supports research to
understand the effects of the environment on human health.  For more
information on environmental health topics, please visit our website at
<http://www.niehs.nih.gov/>.

The National Institutes of Health (NIH) -- "The Nation's Medical
Research Agency" -- includes 27 Institutes and Centers and is a
component of the U.S. Department of Health and Human Services. It is the
primary federal agency for conducting and supporting basic, clinical and
translational medical research, and it investigates the causes,
treatments, and cures for both common and rare diseases. For more
information about NIH and its programs, visit <http://www.nih.gov>.
  
##

This NIH News Release is available online at:
http://www.nih.gov/news/pr/oct2006/niehs-25.htm.

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