The Wilms' tumor 1 protein is a developmental transcription factor that can either activate or repress genes involved in growth, apoptosis and differentiation. How these disparate activities of WT1 are regulated is not clear, but have important implications in determining its role in multiple cancers. Our long-term goal is to understand the mechanisms by which WT1 regulates transcription in development and disease. BASP1 is a critical regulator of WT1 that switches its function from a transcriptional activator to a repressor, and acts by binding to WT1 at the control regions of target genes. We have made the novel finding that the N-terminal myristoylation of BASP1 and the capacity of BASP1 to interact with phosphatidyinositol 4,5-bisphosphate (PIP2) is critical for its transcriptional cosuppressor function. Moreover, our recent data demonstrate that BASP1 is part of a large multiprotein complex that contains the transcriptional repressor prohibitin and histone deacetylase activity. The goal of the current proposal is to provide critical new insights into the mechanisms involved in the regulation of transcription by WT1-BASP1 and the novel role of PIP2.
The specific aims are to; 1. Elucidate the mechanisms by which BASP1-PIP2 interactions control the transcription function of WT1. The role of PIP2 in transcriptional regulation by WT1-BASP1 through chromatin remodeling and RNA polymerase II activity will be investigated using ChIP, transcription analysis, and colocalization approaches. These studies will provide new insights into a novel mechanism of transcriptional repression by gene-specific regulators. 2. Isolate the components of the BASP1 complex and study their function in WT1 regulation. We have recently identified the transcriptional repressor prohibitin and histone deacetylase I as components of the BASP1 complex, which will be analyzed further to determine their mechanism of action. The other components of the complex will be identified and their role in BASP1-mediated transcriptional repression elucidated. 3. Determine the role of the BASP1 complex and PIP2 in the control of differentiation by WT1. A cell line model of podocyte differentiation that is dependent on the activities of WT1 and BASP1 will be employed to identify the critical components of the BASP1 complex, and uncover the role of PIP2 in WT1-dependent gene expression that drives the differentiation process.

Public Health Relevance

The Wilms' tumor 1 protein WT1 acts as a tumor suppressor in childhood kidney cancer, but as an oncogene in adult malignancies. This proposal will study how the WT1 cofactor BASP1 regulates the activities of WT1. The results will provide insights into how WT1 is controlled and aid in the design of new treatments for WT1-dependent tumors.

National Institute of Health (NIH)
National Institute of General Medical Sciences (NIGMS)
Research Project (R01)
Project #
Application #
Study Section
Molecular Genetics C Study Section (MGC)
Program Officer
Sledjeski, Darren D
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
State University of New York at Buffalo
Schools of Arts and Sciences
United States
Zip Code
Perovic, Vladimir; Sumonja, Neven; Gemovic, Branislava et al. (2017) TRI_tool: a web-tool for prediction of protein-protein interactions in human transcriptional regulation. Bioinformatics 33:289-291
Marsh, Lindsey A; Carrera, Samantha; Shandilya, Jayasha et al. (2017) BASP1 interacts with oestrogen receptor ? and modifies the tamoxifen response. Cell Death Dis 8:e2771
Shandilya, Jayasha; Gao, Yankun; Nayak, Tapan K et al. (2016) AP1 transcription factors are required to maintain the peripheral taste system. Cell Death Dis 7:e2433
Shandilya, Jayasha; Medler, Kathryn F; Roberts, Stefan G E (2016) Regulation of AURORA B function by mitotic checkpoint protein MAD2. Cell Cycle 15:2196-2201
Medler, Kathryn F (2015) Honing in on the ATP Release Channel in Taste Cells. Chem Senses 40:449-51
Shandilya, Jayasha; Roberts, Stefan G E (2015) A role of WT1 in cell division and genomic stability. Cell Cycle 14:1358-64
Toska, Eneda; Roberts, Stefan G E (2014) Mechanisms of transcriptional regulation by WT1 (Wilms' tumour 1). Biochem J 461:15-32
Toska, E; Shandilya, J; Goodfellow, S J et al. (2014) Prohibitin is required for transcriptional repression by the WT1-BASP1 complex. Oncogene 33:5100-8
Busch, Maike; Schwindt, Heinrich; Brandt, Artur et al. (2014) Classification of a frameshift/extended and a stop mutation in WT1 as gain-of-function mutations that activate cell cycle genes and promote Wilms tumour cell proliferation. Hum Mol Genet 23:3958-74
Gao, Yankun; Toska, Eneda; Denmon, Dane et al. (2014) WT1 regulates the development of the posterior taste field. Development 141:2271-8

Showing the most recent 10 out of 14 publications