The research program outlined in this proposal is designed to elucidate the genetic basis for Wilms' tumor locus in band p13 of chromosome 11 was originally documented by cytogenetic analysis. Recently, we have isolated and begun the characterization of the gene (WT1) corresponding to this Wilms' tumor locus. The experimental program outlined in this proposal is designed to address the following major questions regarding the WT1 gene: What are the biochemical properties of the WT1 gene product? What are the normal functions of the WT1 gene product? How does inactivation of these functions lead to the occurrence of Wilms' tumor? What other gene products interact with WT1 in regulating cell proliferation? To answer these questions, we intend to proceed with the following approaches: 1. Analysis of the frequency and nature of mutation in the WT1 gene in Wilms' tumors;2. Development of antibody against the WT1 gene products and immunocytochemistry using these antibodies;3. Analysis of the interaction of the WT1 polypeptide with specific DNA sequences;4. Identification of genes transcriptionally controlled by the WT1 gene products; 5. Identification, isolation and characterization of other genes which cooperate with the WT1 gene products 7. Identification of polypeptides which show high affinity for the WT1 gene products; 8. Development and analysis of mouse models for WAGR deletions and Wilms' tumor.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA042063-07
Application #
3795369
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
7
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Type
DUNS #
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Gao, Ang; Shrinivas, Krishna; Lepeudry, Paul et al. (2018) Evolution of weak cooperative interactions for biological specificity. Proc Natl Acad Sci U S A 115:E11053-E11060
Dubbury, Sara J; Boutz, Paul L; Sharp, Phillip A (2018) CDK12 regulates DNA repair genes by suppressing intronic polyadenylation. Nature 564:141-145
Parisi, Tiziana; Balsamo, Michele; Gertler, Frank et al. (2018) The Rb tumor suppressor regulates epithelial cell migration and polarity. Mol Carcinog 57:1640-1650
Sabari, Benjamin R; Dall'Agnese, Alessandra; Boija, Ann et al. (2018) Coactivator condensation at super-enhancers links phase separation and gene control. Science 361:
Chiu, Anthony C; Suzuki, Hiroshi I; Wu, Xuebing et al. (2018) Transcriptional Pause Sites Delineate Stable Nucleosome-Associated Premature Polyadenylation Suppressed by U1 snRNP. Mol Cell 69:648-663.e7
JnBaptiste, Courtney K; Gurtan, Allan M; Thai, Kevin K et al. (2017) Corrigendum: Dicer loss and recovery induce an oncogenic switch driven by transcriptional activation of the oncofetal Imp1-3 family. Genes Dev 31:1066
Hnisz, Denes; Shrinivas, Krishna; Young, Richard A et al. (2017) A Phase Separation Model for Transcriptional Control. Cell 169:13-23
JnBaptiste, Courtney K; Gurtan, Allan M; Thai, Kevin K et al. (2017) Dicer loss and recovery induce an oncogenic switch driven by transcriptional activation of the oncofetal Imp1-3 family. Genes Dev 31:674-687
Suzuki, Hiroshi I; Young, Richard A; Sharp, Phillip A (2017) Super-Enhancer-Mediated RNA Processing Revealed by Integrative MicroRNA Network Analysis. Cell 168:1000-1014.e15
Mori, Munemasa; Hazan, Renin; Danielian, Paul S et al. (2017) Cytoplasmic E2f4 forms organizing centres for initiation of centriole amplification during multiciliogenesis. Nat Commun 8:15857

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