(Applicant's Description) We propose experiments in years 26 to 30 of a successful Program to explore the molecular basis on cell transformation. The six participating laboratories will carry out investigations into the role of viral gene products, interacting cellular proteins, and mutagenesis in cell transformation. The six participating laboratories will carry out investigations into the role of viral gene products, interacting cellular proteins, and mutagenesis in cell transformation. Dr. Miller will continue his studies on the mechanism of viral transactivators that disrupt herpesvirus latency. Dr. DiMaio will continue to analyze the effect of papillomavirus E2 proteins, as well as the viral E6 and E7 oncogenes, on the proliferation of human cervical cancer cells, with the goal of determining the molecular basis for the effects observed. Dr. Glazer will study the mutagenic effects of cytomegalovirus oncogenes that employ a """"""""hit-and-run"""""""" mechanism of cell transformation. In another project centered on mutagenesis, Dr. Sweasy will explore the consequences of cancer-associated mutations in DNA polymerase beta on protein function and cellular physiology. Dr. Maizels' project focuses on chromosomal telomeres and cellular proteins involved in telomere maintenance. Finally, Dr. Steitz will continue her studies establishing the biochemical activities of virally-encoded small RNAs and determining their effects on host cell function. In addition, a protein expression and purification core will provide essential services to the Program. This Program represents the significant commitment of the Yale University School of Medicine and the participating investigators to studies that may well have direct relevance to understanding the cause of human cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
2P01CA016038-26
Application #
2824491
Study Section
Subcommittee G - Education (NCI)
Program Officer
Read-Connole, Elizabeth Lee
Project Start
1979-05-01
Project End
2004-02-29
Budget Start
1999-05-07
Budget End
2000-02-29
Support Year
26
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Yale University
Department
Genetics
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
Zhang, Pengwei; Monteiro da Silva, Gabriel; Deatherage, Catherine et al. (2018) Cell-Penetrating Peptide Mediates Intracellular Membrane Passage of Human Papillomavirus L2 Protein to Trigger Retrograde Trafficking. Cell 174:1465-1476.e13
Inoue, Takamasa; Zhang, Pengwei; Zhang, Wei et al. (2018) ?-Secretase promotes membrane insertion of the human papillomavirus L2 capsid protein during virus infection. J Cell Biol 217:3545-3559
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Singh, Gatikrushna; Fritz, Sarah M; Ranji, Arnaz et al. (2017) Isolation of Cognate RNA-protein Complexes from Cells Using Oligonucleotide-directed Elution. J Vis Exp :
Martinez, Ivan; Hayes, Karen E; Barr, Jamie A et al. (2017) An Exportin-1-dependent microRNA biogenesis pathway during human cell quiescence. Proc Natl Acad Sci U S A 114:E4961-E4970
Lee, Nara; Yario, Therese A; Gao, Jessica S et al. (2016) EBV noncoding RNA EBER2 interacts with host RNA-binding proteins to regulate viral gene expression. Proc Natl Acad Sci U S A 113:3221-6
DiMaio, Daniel (2016) Thank You, Edward. Merci, Louis. PLoS Pathog 12:e1005320

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