The present proposal focuses on the function of a novel gene cp27 in the morphogenesis and molecular signaling that occurs during tooth development. CP27 has been recently cloned from an embryonic stage 11 mouse library and completely sequenced in the applicant's laboratory (Diekwisch et al. 1999). CP27 demonstrates highly restricted expression patterns in two distinct localizations during tooth development: (i) at the epithelial- mesenchymal interface of dental lamina stage tooth germs and (ii) in the stellate reticulum of cap stage tooth organs. The Principal Investigator's preliminary data suggest that CP27 is an extracellular matrix protein of the developing tooth organ and a critical molecular factor in normal tooth morphogenesis. The present proposal is designed (i) to determine the function of CP27 in the morphogenesis and signaling during initial tooth development, and (ii) to establish the role of CP27 in the stellate reticulum in relationship to extracellular matrix synthesis. The long-term goals of this project are to understand the regulatory role of CP27 during tooth morphogenesis through analysis of the tissue specific mechanisms of gene expression.
Four specific aims are proposed to address the hypothesis that CP27 is an extracellular matrix molecule in the developing tooth organ that is critical both to the initiation of tooth morphogenesis and to the morphogenetic control of tooth crown formation.
Specific Aim 1 proposes to determine the temporospatial expression and localization of CP27 in the developing tooth organ.
Specific Aim 2 proposes studies to characterize the mechanism of CP27 regulating cellular proliferation and growth at the onset of tooth development.
Specific Aim 3 will determine the effect of CP27 on apoptosis, anoikis, and cell fate in tooth development.
Specific aim 4 proposes studies to evaluate the role of CP27 controlling cell shape and tissue architecture of the developing tooth organ. The proposed studies will determine the function of CP27 in the epithelia1-mesenchymal interactions that occur during tooth development. Understanding the function of CP27 may provide the basis for the development of novel clinical aids for craniofacial diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
1R01DE013095-01A2
Application #
6285747
Study Section
Oral Biology and Medicine Subcommittee 1 (OBM)
Program Officer
Small, Rochelle K
Project Start
2001-02-01
Project End
2001-09-30
Budget Start
2001-02-01
Budget End
2001-09-30
Support Year
1
Fiscal Year
2001
Total Cost
$61,609
Indirect Cost
Name
Texas A&M University
Department
Other Basic Sciences
Type
Schools of Dentistry
DUNS #
City
College Station
State
TX
Country
United States
Zip Code
77845
Ito, Yoshihiro; Zhang, Youbin; Dangaria, Smit et al. (2011) NF-Y and USF1 transcription factor binding to CCAAT-box and E-box elements activates the CP27 promoter. Gene 473:92-9
Luan, Xianghong; Ito, Yoshihiro; Zhang, Youbin et al. (2010) Characterization of the mouse CP27 promoter and NF-Y mediated gene regulation. Gene 460:8-19
Diekwisch, Thomas G H; Luan, Xianghong; McIntosh, James E (2002) CP27 localization in the dental lamina basement membrane and in the stellate reticulum of developing teeth. J Histochem Cytochem 50:583-6
Diekwisch, Thomas G H; Luan, Xianghong (2002) CP27 function is necessary for cell survival and differentiation during tooth morphogenesis in organ culture. Gene 287:141-7
Luan, X; Diekwisch, T G H (2002) CP27 affects viability, proliferation, attachment and gene expression in embryonic fibroblasts. Cell Prolif 35:207-19