Understanding the mechanism of DNA replication and chromatin inheritance in human cells is a fundamental problem in biology and has direct relevance to cancer research. Alterations to the normal pattern of inheritance can lead to human disease, including cancer. Our studies focus on three specific areas of research that cover different aspects of how a cell inherits chromosomes during cell division. The first area involves the PCNA clamp loader protein, Replication Factor C (RFC) and RFC-related proteins. Biochemical studies are designed to determine the functions of the RFC-like proteins and determine how interact with PCNA-like checkpoint proteins. PCNA is also required for DNA replication dependent chromatin inheritance and inheritance of epigenetically determined states of gene expression. We will investigate the role of PCNA and an associated protein called Chromatin Assembly Factor-1 (CAF-1) in these processes. The identification of other proteins that cooperate with PCNA and CAF-1 will contribute to an understanding of how allele-specific inactivation of gene expression occurs, a process that often leads to loss of tumor suppressor gene function during progression toward cancer. Finally, we will continue studies on the role of human ORC in establishing the sites in chromosomes for nitiation of DNA replication. ORC cooperates with other initiation proteins to form a pre-replication complex in cells and this complex renders chromosomes competent for initiation of DNA replication. We intend to identify ORC binding proteins and characterize their role in chromosome inheritance. These studies on chromosome inheritance are directly relevant to the overall goals of the Program Project.
On, Kin Fan; Jaremko, Matt; Stillman, Bruce et al. (2018) A structural view of the initiators for chromosome replication. Curr Opin Struct Biol 53:131-139 |
Knott, Simon R V; Wagenblast, Elvin; Khan, Showkhin et al. (2018) Asparagine bioavailability governs metastasis in a model of breast cancer. Nature 554:378-381 |
Shamay, Yosi; Shah, Janki; I??k, Mehtap et al. (2018) Quantitative self-assembly prediction yields targeted nanomedicines. Nat Mater 17:361-368 |
Tramentozzi, Elisa; Ferraro, Paola; Hossain, Manzar et al. (2018) The dNTP triphosphohydrolase activity of SAMHD1 persists during S-phase when the enzyme is phosphorylated at T592. Cell Cycle 17:1102-1114 |
Arun, Gayatri; Diermeier, Sarah D; Spector, David L (2018) Therapeutic Targeting of Long Non-Coding RNAs in Cancer. Trends Mol Med 24:257-277 |
Tarumoto, Yusuke; Lu, Bin; Somerville, Tim D D et al. (2018) LKB1, Salt-Inducible Kinases, and MEF2C Are Linked Dependencies in Acute Myeloid Leukemia. Mol Cell 69:1017-1027.e6 |
Xu, Yali; Milazzo, Joseph P; Somerville, Tim D D et al. (2018) A TFIID-SAGA Perturbation that Targets MYB and Suppresses Acute Myeloid Leukemia. Cancer Cell 33:13-28.e8 |
Huang, Yu-Han; Klingbeil, Olaf; He, Xue-Yan et al. (2018) POU2F3 is a master regulator of a tuft cell-like variant of small cell lung cancer. Genes Dev 32:915-928 |
Livshits, Geulah; Alonso-Curbelo, Direna; Morris 4th, John P et al. (2018) Arid1a restrains Kras-dependent changes in acinar cell identity. Elife 7: |
Tiriac, Hervé; Belleau, Pascal; Engle, Dannielle D et al. (2018) Organoid Profiling Identifies Common Responders to Chemotherapy in Pancreatic Cancer. Cancer Discov 8:1112-1129 |
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