Bmi-1 and the other Polycomb Group (PcG) genes are important epigenetic regulators of cell survival. In spite of this realization the possibility that they may play a role maintaining epidermal keratinocyte survival has not been considered. This is likely because this area is now at the forefront of discovery since the importance of these proteins was only recently appreciated. Our preliminary studies show that Bmi-1 is present in epidermis and that elevated Bmi-1 promotes keratinocyte proliferation and survival. We also show that Bmi-1 is elevated in diseases such as psoriasis and cancer, suggesting a role in the genesis of these disorders. We have created an animal model that develops a thickened hyperproliferative epidermis in response to Bmi-1 - a finding that suggests a functional role in epidermal physiology.
Specific Aim 1 is designed to assess the impact of Bmi-1 in epidermal keratinocyte proliferation and survival and to study the chromatin modification events associated with Bmi-1 dependent suppression of involucrin gene expression.
Specific Aim 2 is designed to characterize the anti-apoptosis effect of Bmi-1.
Specific Aim 3 will identify Bmi-1 domain(s) that are responsible for the physiological changes in apoptosis, cell proliferation and gene expression.
Specific Aim 4 utilizes transgenic mice which express Bmi-1 in epidermis to assess the in vivo role of this epigenetic regulator. We believe that these studies are innovative and "high impact" because they will change the classical dogma regarding the role of Bmi-1 and other PcG genes in tissues. NARRATIVE: The Bmi-1 Polycomb Group (PcG) gene is an important epigenetic regulator that enhances stem cell survival. However, a role in epidermis has not been studied. We show that Bmi-1 is expressed in epidermis, promotes cell cycle progression, inhibits apoptosis, has non-stem cell functions, drives hyperproliferation in mouse epidermis, and is likely to be involved in the genesis of hyperproliferative skin disease. These studies argue that Bmi-1 has a physiologically important role in epidermis. These studies are innovative and "high impact" because they will change the classical dogma regarding the role of PcG genes in tissues.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
5R01AR053851-05
Application #
8228180
Study Section
Arthritis, Connective Tissue and Skin Study Section (ACTS)
Program Officer
Baker, Carl
Project Start
2008-05-01
Project End
2013-02-28
Budget Start
2012-03-01
Budget End
2013-02-28
Support Year
5
Fiscal Year
2012
Total Cost
$389,760
Indirect Cost
$129,920
Name
University of Maryland Baltimore
Department
Biochemistry
Type
Schools of Medicine
DUNS #
188435911
City
Baltimore
State
MD
Country
United States
Zip Code
21201
Eckert, Richard L; Kaartinen, Mari T; Nurminskaya, Maria et al. (2014) Transglutaminase regulation of cell function. Physiol Rev 94:383-417
Saha, Kamalika; Adhikary, Gautam; Kanade, Santosh R et al. (2014) p38? regulates p53 to control p21Cip1 expression in human epidermal keratinocytes. J Biol Chem 289:11443-53
Eckert, Richard L; Adhikary, Gautam; Balasubramanian, Sivaprakasam et al. (2013) Biochemistry of epidermal stem cells. Biochim Biophys Acta 1830:2427-34
Chew, Yap Ching; Adhikary, Gautam; Xu, Wen et al. (2013) Protein kinase C ýý increases Kruppel-like factor 4 protein, which drives involucrin gene transcription in differentiating keratinocytes. J Biol Chem 288:17759-68
Balasubramanian, Sivaprakasam; Chew, Yap Ching; Eckert, Richard L (2011) Sulforaphane suppresses polycomb group protein level via a proteasome-dependent mechanism in skin cancer cells. Mol Pharmacol 80:870-8
Choudhury, Subhasree Roy; Balasubramanian, Sivaprakasam; Chew, Yap Ching et al. (2011) (-)-Epigallocatechin-3-gallate and DZNep reduce polycomb protein level via a proteasome-dependent mechanism in skin cancer cells. Carcinogenesis 32:1525-32
Eckert, Richard L; Adhikary, Gautam; Rorke, Ellen A et al. (2011) Polycomb group proteins are key regulators of keratinocyte function. J Invest Dermatol 131:295-301