EXCEED THE SPACE PROVIDED. Transforming growth factor beta (TGFbeta) related ligands regulate many aspects of cell differentiation and function, and components of the signaling pathway act as tumor suppressors involved in human cancers. In the nematode C. elegans, a TGFbeta-related signaling pathway, the dbl-1 pathway, controls body size and male tail morphogenesis. Studies of this pathway have previously been fruitful in identifying conserved signaling components, including the Smad signal transducers SMA-2, SMA-3, and SMA-4. Smad proteins are cytoplasmic components that are directly regulated by activated TGFbeta receptors to translocate into the nucleus and generate transcriptional responses. Given the diversity and cell type specificity of TGFbeta responses, this simple Smad signaling mechanism must require modulation by other signaling components. To identify additional components of the dbl-1 pathway and in particular those that confer specific pathway responses, a forward genetic screen for additional mutations affecting body size was performed. This screen identified several new genes, including sma-20. Preliminary analysis of sma-20 mutant phenotypes suggests that it plays spatially and temporally specific roles in dbl-1 signaling. To characterize the roles of sma-20 in body size regulation, male tail development, and TGFbeta-related signal transduction, we propose to use genetic, molecular, and phenotypic analyses of sma-20. Our goals are to (1) determine the complete loss of function (null) phenotype of sma-20;(2) map and positionally clone sma-20;and (3) analyze sma-20 cellular and temporal focus of action. These experiments will provide educational and scientific training opportunities for a graduate student and one or more undergraduate students at Queens College, CUNY. Since TGFbeta superfamily ligands, their receptors, the Smads, and Schnurri are all conserved through distant animal phyla, studying new components in a genetically tractable model organism should provide insight into their functions in other organisms as well. PERFORMANCE SITE ========================================Section End===========================================

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
3R15GM073678-01S1
Application #
7887223
Study Section
Development - 1 Study Section (DEV)
Project Start
2009-08-03
Project End
2011-03-31
Budget Start
2009-08-03
Budget End
2011-03-31
Support Year
1
Fiscal Year
2009
Total Cost
$97,094
Indirect Cost
Name
Queens College
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
619346146
City
Flushing
State
NY
Country
United States
Zip Code
11367
Yin, Jianghua; Madaan, Uday; Park, Amy et al. (2015) Multiple cis elements and GATA factors regulate a cuticle collagen gene in Caenorhabditis elegans. Genesis 53:278-84
Gumienny, Tina L; Savage-Dunn, Cathy (2013) TGF-? signaling in C. elegans. WormBook :1-34
Liang, Jun; Xiong, Sheng; Savage-Dunn, Cathy (2013) Using RNA-mediated interference feeding strategy to screen for genes involved in body size regulation in the nematode C. elegans. J Vis Exp :
Savage-Dunn, Cathy; Yu, Ling; Gill, Kwesi et al. (2011) Non-stringent tissue-source requirements for BMP ligand expression in regulation of body size in Caenorhabditis elegans. Genet Res (Camb) 93:427-32
Fernando, Thilini; Flibotte, Stephane; Xiong, Sheng et al. (2011) C. elegans ADAMTS ADT-2 regulates body size by modulating TGF? signaling and cuticle collagen organization. Dev Biol 352:92-103