The long-term goal of this study is to understand the molecular mechanism of mammalian Hedgehog (Hh) signal transduction. Aberrant Hh signaling has been associated with various human cancers and birth defects. Recent evidence indicates that several aspects of Hh signaling are not conserved between invertebrates and vertebrates. Not only have the roles of some of the main players changed in vertebrates, but also their genetic interactions and the mode of signal transduction have been modified. Further, primary cilia appear to play a major role in mammalian and not Drosophila Hh signaling. These findings highlight the importance of elucidating the functions of mammalian Hh pathway components directly in order to further understand vertebrate Hh signal transduction. This proposal focuses on one critical player in mammalian Hh signal transduction, Suppressor of Fused (Sufu), and will define the mechanism of Sufu in regulating the functions of Gli transcription factors, the sole mediators of Hh signaling during mammalian development. We propose the following specific aims: 1) Define the role of Sufu in controlling ciliary localization of Gli2. 2) Elucidate the molecular mechanism of Sufu-mediated Gli3 protein stabilization. 3) Delineate the requirement of primary cilia in Sufu- or SPOP-mediated Gli protein function. 4) Test the hypothesis that Sufu interacts with Kif7, a kinesin family member, in modulating mammalian Hh signaling. A combination of cell-based assays, genetic studies using knockout mice and protein biochemistry will be employed to address these central issues. These studies will provide new mechanistic insights into how the mammalian Hh signal is transduced in responsive cells 7.

Public Health Relevance

Aberrant Hedgehog (Hh) signaling is associated with cancers and birth defects. Elucidating how the Hh signal is transduced is critical to understanding the underlying mechanisms of Hh-related diseases as well as identifying potential targets for diagnosis and rational therapies. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM085097-01
Application #
7506250
Study Section
Intercellular Interactions (ICI)
Program Officer
Anderson, Richard A
Project Start
2008-08-01
Project End
2012-07-31
Budget Start
2008-08-01
Budget End
2009-07-31
Support Year
1
Fiscal Year
2008
Total Cost
$309,000
Indirect Cost
Name
University of California San Francisco
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Lin, Chuwen; Chen, Miao-Hsueh; Yao, Erica et al. (2014) Differential regulation of Gli proteins by Sufu in the lung affects PDGF signaling and myofibroblast development. Dev Biol 392:324-33
Lin, Chuwen; Yao, Erica; Wang, Kevin et al. (2014) Regulation of Sufu activity by p66? and Mycbp provides new insight into vertebrate Hedgehog signaling. Genes Dev 28:2547-63
Nozawa, Yoko Inès; Lin, Chuwen; Chuang, Pao-Tien (2013) Hedgehog signaling from the primary cilium to the nucleus: an emerging picture of ciliary localization, trafficking and transduction. Curr Opin Genet Dev 23:429-37