The stratified mammalian epidermis develops from somatic ectoderm by the progressive addition and differentiation of superficial epidermal layers (1). After the initial morphogenesis, the epidermis is maintained by homeostatic mechanisms whereby keratinocytes move from the proliferating basal cell layer towards the surface as they undergo a series of differentiation steps, ultimately undergoing cell death. One role of keratinocyte differentiation is the formation of an effective permeability barrier, which depends on the regulated expression of a large battery of genes encoding components of the cornified and granular layers (2). Under funding by the parent grant, we are using molecular biology to investigate the role of a single transcription factor, the Grainyhead-like transcription factor Get1/Grhl3 (3-5), in epidermal differentiation. In contrast, in this revision application, we propose a systems biology approach to computationally generate transcriptional regulatory network for the process of epidermal differentiation. Thus, this application leads to a new direction and differs from the parent grant in two important ways: First, it expands the scope of the study to transcriptional regulatory networks in epidermal development in general, and second, it incorporates the methods of systems biology;thus the application is consistent with one of the key emphasis areas of this RFA (Developmental Biology - Systems biology). The specific goals are to: 1) Generate global gene expression data over the time course of epidermal keratinocyte differentiation;and 2) Use the time course gene expression data from 1, other genome-wide expression data, DNA motif information, functional annotation, and literature mining to infer transcriptional networks in epidermal differentiation. The goal of this project is also to build a new interdisciplinary team between the Andersen laboratory, whose primary expertise is in molecular/developmental biology, and Alex Ihler, a new assistant professor whose primary expertise is in graphical models, Bayesian inference methods, machine learning, and data mining. The contributions of the Ihler group -- the mathematical modeling required to define the networks -- will allow approaches and advances in our understanding of epidermal differentiation that would not be attainable without this collaboration.

Public Health Relevance

Defective epidermal differentiation and disrupted barrier formation are salient features of several skin diseases, including childhood eczema and psoriasis. With the definition of networks important for these processes, we expect to discover new diagnostic approaches and treatment targets.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
3R01AR044882-13S1
Application #
7776854
Study Section
Special Emphasis Panel (ZAR1-CHW-D (M1))
Program Officer
Baker, Carl
Project Start
1998-08-01
Project End
2010-07-31
Budget Start
2009-09-18
Budget End
2010-07-31
Support Year
13
Fiscal Year
2009
Total Cost
$146,526
Indirect Cost
Name
University of California Irvine
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
046705849
City
Irvine
State
CA
Country
United States
Zip Code
92697
Plikus, Maksim V; Andersen, Bogi (2018) Skin as a window to body-clock time. Proc Natl Acad Sci U S A 115:12095-12097
Klein, Rachel Herndon; Hu, William; Kashgari, Ghaidaa et al. (2017) Characterization of enhancers and the role of the transcription factor KLF7 in regulating corneal epithelial differentiation. J Biol Chem 292:18937-18950
Klein, Rachel Herndon; Stephens, Denise N; Ho, Hsiang et al. (2016) Cofactors of LIM Domains Associate with Estrogen Receptor ? to Regulate the Expression of Noncoding RNA H19 and Corneal Epithelial Progenitor Cell Function. J Biol Chem 291:13271-85
Spitler, Ryan; Ho, Hsiang; Norpetlian, Frederique et al. (2015) Combination of low level light therapy and nitrosyl-cobinamide accelerates wound healing. J Biomed Opt 20:051022
Gordon, William M; Zeller, Michael D; Klein, Rachel H et al. (2014) A GRHL3-regulated repair pathway suppresses immune-mediated epidermal hyperplasia. J Clin Invest 124:5205-18
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Salmans, Michael L; Yu, Zhengquan; Watanabe, Kazuhide et al. (2014) The co-factor of LIM domains (CLIM/LDB/NLI) maintains basal mammary epithelial stem cells and promotes breast tumorigenesis. PLoS Genet 10:e1004520
Peyrard-Janvid, Myriam; Leslie, Elizabeth J; Kousa, Youssef A et al. (2014) Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development. Am J Hum Genet 94:23-32
Watanabe, Kazuhide; Villarreal-Ponce, Alvaro; Sun, Peng et al. (2014) Mammary morphogenesis and regeneration require the inhibition of EMT at terminal end buds by Ovol2 transcriptional repressor. Dev Cell 29:59-74
Bhandari, A; Gordon, W; Dizon, D et al. (2013) The Grainyhead transcription factor Grhl3/Get1 suppresses miR-21 expression and tumorigenesis in skin: modulation of the miR-21 target MSH2 by RNA-binding protein DND1. Oncogene 32:1497-507

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