The FGF family of signaling molecules plays a central role in the regulation of many aspects of vertebrate embryogenesis, and is also important in the control of physiological and pathological processes in the adult. There is substantial evidence from previous genetic studies that one member of the FGF family, FGF8, is essential at multiple stages of embryogenesis. This proposal is focused on three key developmental processes that are dependent on FGF8 signaling: left-right axis- determination, limb development, and kidney development. The experiments proposed are aimed at using a genetic approach to elucidate the function of FgJ8 and other FGF family members in these processes. They take advantage of recent advances in methods for analyzing gene function in mice, including conditional loss- and gain-of-function in specific tissues, and reporter alleles for gene expression and protein distribution.
Each Specific Aim i ncludes the development of new lines of transgenic mice that will not only make it possible to answer specific questions and test hypotheses about these particular processes, but will also be extremely useful as tools for studies of many other aspects of vertebrate development in laboratories throughout the scientific community. The results of these studies should provide a deeper understanding of the mechanisms involved in establishing the basic body plan and the formation of limbs and kidneys. The information obtained will be relevant to understanding the mechanism of human development and the etiology of human birth defects, chronic diseases, and various forms of adult disease that originate during gestation.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD034380-07
Application #
6636927
Study Section
Mammalian Genetics Study Section (MGN)
Program Officer
Javois, Lorette Claire
Project Start
1996-12-18
Project End
2006-05-31
Budget Start
2003-06-01
Budget End
2004-05-31
Support Year
7
Fiscal Year
2003
Total Cost
$384,347
Indirect Cost
Name
University of California San Francisco
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Mariani, Francesca V; Ahn, Christina P; Martin, Gail R (2008) Genetic evidence that FGFs have an instructive role in limb proximal-distal patterning. Nature 453:401-5
Lu, Pengfei; Minowada, George; Martin, Gail R (2006) Increasing Fgf4 expression in the mouse limb bud causes polysyndactyly and rescues the skeletal defects that result from loss of Fgf8 function. Development 133:33-42
Grieshammer, Uta; Cebrian, Cristina; Ilagan, Roger et al. (2005) FGF8 is required for cell survival at distinct stages of nephrogenesis and for regulation of gene expression in nascent nephrons. Development 132:3847-57
Lewandoski, M; Sun, X; Martin, G R (2000) Fgf8 signalling from the AER is essential for normal limb development. Nat Genet 26:460-3
Sun, X; Lewandoski, M; Meyers, E N et al. (2000) Conditional inactivation of Fgf4 reveals complexity of signalling during limb bud development. Nat Genet 25:83-6
Sun, X; Meyers, E N; Lewandoski, M et al. (1999) Targeted disruption of Fgf8 causes failure of cell migration in the gastrulating mouse embryo. Genes Dev 13:1834-46
Meyers, E N; Martin, G R (1999) Differences in left-right axis pathways in mouse and chick: functions of FGF8 and SHH. Science 285:403-6
Martinez, S; Crossley, P H; Cobos, I et al. (1999) FGF8 induces formation of an ectopic isthmic organizer and isthmocerebellar development via a repressive effect on Otx2 expression. Development 126:1189-200
Trumpp, A; Depew, M J; Rubenstein, J L et al. (1999) Cre-mediated gene inactivation demonstrates that FGF8 is required for cell survival and patterning of the first branchial arch. Genes Dev 13:3136-48
Neubuser, A; Peters, H; Balling, R et al. (1997) Antagonistic interactions between FGF and BMP signaling pathways: a mechanism for positioning the sites of tooth formation. Cell 90:247-55