? The long-term objective of this application for competing continuation of the grant (1R01 RR15402) is to make a complete description of the spatial and temporal expression of a vertebrate genome. ? ? The zebrafish (Danio rerio) is the model organism used to achieve this goal. This vertebrate species displays many technical advantages allowing high throughput analyses of gene expression patterns by whole mount in situ hybridization on developing embryos. The work funded by the current application has already allowed the screening of 13,000 cDNAs corresponding to 8,000 different genes. This application proposes to increase the size of the screen to analyse, in 3 years, the expression of 15,000 genes. All these data will be described and made available to public into the zebrafish community database at the University of Oregon (http://zfin.org). A precise description of gene expression patterns will be provided on this web site in the gene expression section. This description will include keywords, text and a set of annotated pictures of embryos at different developmental stages (from gastrulation stage to hatching). Genes identified in this study will also be freely available upon request at the zebrafish International Resource center. ? ? The resources generated in this project will provide a large collection of cell and/or tissue specific markers usable for the analysis of embryonic development and for the establishment of a """"""""molecular anatomy"""""""". It will provide starting points for functional analyses (by gain or loss of function experiments and reverse genetic). Finally, many of the genes identified in this screen are orthologues of human genes of unknown function. The establishment of the spatial and temporal expression of these genes in fish will provide a first set of data that will help to analyze their function during mammalian embryonic development. This will provide insights to better understand both normal and pathological human development. ? ?

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Research Project (R01)
Project #
2R01RR015402-04
Application #
6720426
Study Section
Genome Study Section (GNM)
Program Officer
Chang, Michael
Project Start
2001-02-05
Project End
2007-06-30
Budget Start
2004-07-01
Budget End
2005-06-30
Support Year
4
Fiscal Year
2004
Total Cost
$402,117
Indirect Cost
Name
Lab de Genetique Moleculaire Des Eucaryo
Department
Type
DUNS #
City
Strasbourg
State
Country
France
Zip Code
Krug 2nd, Randall G; Clark, Karl J (2015) Elucidating cannabinoid biology in zebrafish (Danio rerio). Gene 570:168-79
Yao, Zizhen; Farr 3rd, Gist H; Tapscott, Stephen J et al. (2013) Pbx and Prdm1a transcription factors differentially regulate subsets of the fast skeletal muscle program in zebrafish. Biol Open 2:546-55
Fernando, Carol A; Conrad, Patricia A; Bartels, Cynthia F et al. (2010) Temporal and spatial expression of CCN genes in zebrafish. Dev Dyn 239:1755-67
Maves, Lisa; Tyler, Ashlee; Moens, Cecilia B et al. (2009) Pbx acts with Hand2 in early myocardial differentiation. Dev Biol 333:409-18
Walters, Kevin B; Dodd, M Ernest; Mathias, Jonathan R et al. (2009) Muscle degeneration and leukocyte infiltration caused by mutation of zebrafish Fad24. Dev Dyn 238:86-99
Galloway, Jenna L; Wingert, Rebecca A; Thisse, Christine et al. (2008) Combinatorial regulation of novel erythroid gene expression in zebrafish. Exp Hematol 36:424-32
Thisse, Christine; Thisse, Bernard (2008) High-resolution in situ hybridization to whole-mount zebrafish embryos. Nat Protoc 3:59-69
Wingert, Rebecca A; Selleck, Rori; Yu, Jing et al. (2007) The cdx genes and retinoic acid control the positioning and segmentation of the zebrafish pronephros. PLoS Genet 3:1922-38
Maves, Lisa; Waskiewicz, Andrew Jan; Paul, Biswajit et al. (2007) Pbx homeodomain proteins direct Myod activity to promote fast-muscle differentiation. Development 134:3371-82
Mathias, Jonathan R; Dodd, M Ernest; Walters, Kevin B et al. (2007) Live imaging of chronic inflammation caused by mutation of zebrafish Hai1. J Cell Sci 120:3372-83

Showing the most recent 10 out of 29 publications