The central theme of this program grant is regulation of gene expression by oncogenes. We will address this theme by (a) isolation of new oncogenes, (b) study of the regulation of known oncogenes, (c) study of the mechanism by which oncogenes can affect transcription of other genes, (d) definition and purification of factors which regulate promoters, and (e) identification of factors which recognize enhancer elements in a cell type specific fashion. The exciting new aspect of this theme is that part of the problem of cancer can now be phrased in the context of the action and control of known genes. At the moment, the set of oncogenes that have been identified number about 25-30. These genes are probably involved in essential cellular processes and are altered in transformed cells in terms of either level of activity or type of activity. The next frontier in research on oncogenesis is to determine how these oncogene proteins function biochemically and affect alterations in cell behavior. This is a challenging problem as little is known about the cellular processes, particularly nuclear processes, that regulate cell growth. Success in this endeavor will require the close interaction and collaboration of scientists interested in: the action of oncogenes, the intracellular signals generated by peptide hormones, the regulation of gene expression and the biochemistry of nuclear processes such as transcription. Understanding the activities of oncogenes at this molecular level will reveal how they collaborate in transformation and the relationships of transformation to processes such as differentiation

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA042063-04
Application #
3093911
Study Section
Cancer Special Program Advisory Committee (CAK)
Project Start
1986-05-01
Project End
1991-04-30
Budget Start
1989-05-01
Budget End
1990-04-30
Support Year
4
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Type
Organized Research Units
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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