Zebrafish mutagenesis screens hold promise for identifying genes underlying phenotypes relevant to development and to disease. Associating phenotype and genotype will require development of genotyping tools matched in throughput to the scale of these screens. This proposal addresses this gap in response to the program announcement """"""""Tools for Genetic Studies in Zebrafish."""""""" We propose to apply our extensive experience in high-throughput genotyping to create a shared genome-wide mapping resource for the zebrafish community. The Principal Investigator has developed state-of-the-art genotyping technologies and informatics tools that are currently operational and directly applicable in zebrafish mapping. We have completed approximately one million genotypes, developed >75 fluorescent simple tandem repeat (STR) marker panels (including a robust genome-wide set for human genetic mapping), discovered and genotyped comprehensive single nucleotide polymorphisms (SNP) maps across candidate genes in large-scale human studies, and are now performing a genome-wide mouse SNP scan. Here we propose development of shared zebrafish mapping resources: robust genome-wide marker sets for high-throughput genetic screens, and a public bioinformatics system to organize and design custom assays for subsequent fine mapping.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK065637-05
Application #
7236170
Study Section
Special Emphasis Panel (ZRG1-CDF-5 (50))
Program Officer
Rasooly, Rebekah S
Project Start
2003-08-01
Project End
2010-05-31
Budget Start
2007-06-01
Budget End
2010-05-31
Support Year
5
Fiscal Year
2007
Total Cost
$332,437
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
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Melville, David B; Montero-Balaguer, Mercedes; Levic, Daniel S et al. (2011) The feelgood mutation in zebrafish dysregulates COPII-dependent secretion of select extracellular matrix proteins in skeletal morphogenesis. Dis Model Mech 4:763-76
Bradley, Kevin M; Breyer, Joan P; Melville, David B et al. (2011) An SNP-Based Linkage Map for Zebrafish Reveals Sex Determination Loci. G3 (Bethesda) 1:3-9
Bradley, Kevin M; Elmore, J Bradford; Breyer, Joan P et al. (2007) A major zebrafish polymorphism resource for genetic mapping. Genome Biol 8:R55