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RFA on MOUSE PHENOTYPING for DEVELOPMENTAL AND
FERTILITY DEFECTS (HD-01-020)
The National Institute of Child Health and Human Development (NICHD)
has issued a Request for Applications (RFA) to phenotype mutant
mouse strains with developmental and fertility defects and to characterize
the mutations responsible for their defects. Projects should be
designed to characterize mouse strains with defects in development
and reproduction so as to isolate new alleles of known genes and
identify new genes that are involved in the processes of development
and fertility. The mouse strains to be characterized should be obtained
from existing mouse mutagenesis projects. Appropriate sources of
mutant strains include both small-scale mutagenesis projects and
large-scale mutagenesis facilities, such as the NIH-funded mouse
mutagenesis and phenotyping facilities at Baylor College of Medicine,
Northwestern University, Jackson Laboratory, and the University
of Tennessee. Characterizing these mouse strains, and their mutations,
is expected to help elucidate the basic cellular, molecular, and
genetic mechanisms that direct embryonic and post-embryonic development,
as well as yield insights into the mechanisms that control fertility.
These projects should identify and obtain mutant mouse strains with
disrupted development and fertility, phenotype the strains to provide
a detailed characterization of the defects, and characterize the
mutations and the genes responsible for the defects. The phenotypic
characterization may also include high-throughput screens to identify
a broad range of general features of these strains, where appropriate.
The detailed characterization should describe the specific cellular,
molecular, and genetic features of the defects, whereas high-throughput
screens, if included, should provide a general overview of the biological
features of the animals with these defects. Characterization of
the mutations and genes should include analyses to increase the
value of the mutants to the scientific community, such as genetic
mapping to localize the mutations within the genome.
These projects will be part of NIH's initiative to determine the
function of mammalian genes. Accordingly, their activities will
be coordinated with related facilities, including the NIH-funded
Mouse Mutagenesis and Phenotyping: Developmental Defects Facility
at Baylor College of Medicine (http://www.mouse-genome.bcm.tmc.edu/ENU/MutagenesisProj.asp).
Additionally, the mutant strains, phenotypic and genetic information,
protocols, assays, assessment criteria, and other materials and
information generated by projects funded under this RFA will be
made available to the wider biomedical community. Further information
about NIH initiatives on mouse genomics and genetics resources is
available at http://www.nih.gov/science/mouse.
The RFA will use the cooperative agreement grant mechanism (U01),
and will provide up to $3 million (total cost) for the first year
of funding. NICHD intends to fund about four grants. Applications
for both small and large projects are encouraged. Letters of Intent
are due by February 11, 2002. The applications are due on March
13, 2002, and the earliest possible funding date is September 30,
2002. The full text of the RFA is available at: http://grants.nih.gov/grants/guide/rfa-files/RFA-HD-01-020.html.
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