The transforming growth factor-beta (TGF-beta) signaling pathway is involved in many cellular processes ranging from proliferation, differentiation, development, and programmed cell death. Disruption of this pathway can result in a variety of diseases and is often an early step in the progression of cancers. The TGF-beta signaling pathway is highly conserved and is required in worms, flies, frogs, mice, and men. Since these growth factors work similarly in all of these organisms, what we learn about their function in simpler organisms should be relevant in other species, including humans. In this research project, I propose to explore the role of lon-2, a gene in C. elegans (a nematode worm), in the TGF-beta signaling pathway and its mechanism of action. My studies in this model organism should contribute to a better understanding of the signaling pathway in general and may provide for human therapies for TGF-beta-related diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM066445-02
Application #
6640490
Study Section
Special Emphasis Panel (ZRG1-F05 (20))
Program Officer
Tompkins, Laurie
Project Start
2002-08-01
Project End
2004-09-30
Budget Start
2003-08-01
Budget End
2004-09-30
Support Year
2
Fiscal Year
2003
Total Cost
$46,420
Indirect Cost
Name
Rutgers University
Department
Type
Organized Research Units
DUNS #
001912864
City
New Brunswick
State
NJ
Country
United States
Zip Code
08901
Gumienny, Tina L; Macneil, Lesley; Zimmerman, Cole M et al. (2010) Caenorhabditis elegans SMA-10/LRIG is a conserved transmembrane protein that enhances bone morphogenetic protein signaling. PLoS Genet 6:e1000963
Gumienny, Tina L; MacNeil, Lesley T; Wang, Huang et al. (2007) Glypican LON-2 is a conserved negative regulator of BMP-like signaling in Caenorhabditis elegans. Curr Biol 17:159-64