My long-term interest is to elucidate molecular mechanisms governing mammalian development and selfrenewal and differentiation of stem cells. Here, I employ skin as a model system to investigate functions of a family of small RNA molecules, microRNAs, in embryonic development. Such research will provide future basis for clinical use of skin stem cells in regenerative medicine and for developing methods for prevention and treatment of skin cancer. In the K99 phase of this project, I showed the differential expression pattern of miR-203 during embryonic skin development and demonstrated its critical role in repressing the prolifeartive potential of epidermal stem cells once these cells enter the terminal differentiation program. Furthermore, I identified p63, an essential gene for the maintenance of epidermal stem cells, as a key target of miR-203. These studies provide the first example of an individual microRNA that plays an important role in skin. In the ROO phase, I will pursue the initial studies and probe more deeply into this hitherto unexplored area of skin biology. Specifically, I will first utilize accurate isolation of specific skin lineages by fluorescen-actived cell sorting method and high-throughput microan-ay profiling of microRNA expression to identity differentially expressed microRNAs in specific epidermal and hair lineages. I will then use in situ hybridization method to monitor the expression patterns of these microRNAs during skin development. This study will reveal diffemtial expression of microRNAs in high resolution and provide candidates for future functional studies. To further explore the mechanism of miR-203's functions, I will establish an in vivo mouse model to identify the direct target of miR-203. This study will elucidate the molecular mechanisms of miR-203's functions and improve our understanding of microRNA target recognition. Collectively, these studies will also pave the way for me to establish my independent research program and prepare preliminar data for a R01 application.

Public Health Relevance

Skin, the outermost ban'ier of mammals, protects body from hazards in the environment and keeps fluids within the body. Understanding regulatory networks mediated by microRNAs during embryonic skin development and self-renewal and differentiation of skin stem cells during adulthopd will enhance our knowledge of nomnal skin development and of progression to various skin disorders including skin cancer.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Transition Award (R00)
Project #
5R00AR054704-05
Application #
8010638
Study Section
Special Emphasis Panel (NSS)
Program Officer
Baker, Carl
Project Start
2009-01-20
Project End
2011-12-31
Budget Start
2011-01-01
Budget End
2011-12-31
Support Year
5
Fiscal Year
2011
Total Cost
$248,764
Indirect Cost
Name
University of Colorado at Boulder
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
007431505
City
Boulder
State
CO
Country
United States
Zip Code
80309
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Jackson, Sarah J; Zhang, Zhaojie; Feng, Dejiang et al. (2013) Rapid and widespread suppression of self-renewal by microRNA-203 during epidermal differentiation. Development 140:1882-91
Wang, Dongmei; Zhang, Zhaojie; O'Loughlin, Evan et al. (2013) MicroRNA-205 controls neonatal expansion of skin stem cells by modulating the PI(3)K pathway. Nat Cell Biol 15:1153-63
Wang, Dongmei; Zhang, Zhaojie; O'Loughlin, Evan et al. (2012) Quantitative functions of Argonaute proteins in mammalian development. Genes Dev 26:693-704
Yi, Rui; Fuchs, Elaine (2012) A miR image of stem cells and their lineages. Curr Top Dev Biol 99:175-99
Yi, Rui; Fuchs, Elaine (2011) MicroRNAs and their roles in mammalian stem cells. J Cell Sci 124:1775-83
Yi, R; Fuchs, E (2010) MicroRNA-mediated control in the skin. Cell Death Differ 17:229-35