Hilary Coller
Phone: 3108253483
Office: 5145 Terasaki Life Sciences
Lab: 5128 Terasaki Life Sciences

Education

B.A., Harvard University, Biochemistry And Molecular Biology 1989
M.S., Massachusetts Institute of Technology, Technology And Policy 1991
M.S., Massachusetts Institute of Technology, Toxicology 1993
Ph.D., Massachusetts Institute of Technology, Toxicology 2014

Research Interests

Because uncontrolled cell division is so dangerous for an organism, cells must know not only when to divide, but?crucially?when not to. Cell division arrest prevents tumors and maintains the proper form of tissues. Many cells must also retain the ability to start dividing again when conditions are right, e.g., when the organism must grow, or a damaged tissue must be repaired. A cell in such a temporary, non-dividing state is said to be ?quiescent.? Quiescence is a common state for many somatic cells, including fibroblasts, lymphocytes, hematopoietic stem cells, and even dormant tumor cells. Failure to appropriately regulate the transition between quiescence and proliferation underlies several common and lethal disorders, including cancer and chronic wounds. My research is focused on understanding the molecular basis of quiescence using in vitro models, mouse models and human patients.

Selected Publications

Nouvong, A., Ambrus A.M., Zhang, E.R., Hultman, L. and Coller, H.A., "Reactive oxygen species and bacterial biofilms in diabetic wound healing", Physiological Genomics (2016). [link]

Rabinowitz, J. and Coller, H.A., "Partners in the Warburg effect", eLife (2016). [link]

Mitra, M., Johnson, E.L., and Coller, H. A., "Alternative polyadenylation can regulate post-translational membrane localization", Trends in Cell and Molecular Biology 10: 37-47 (2015). [link]

Corney, D., and Coller, H.A., "On form and function: Does chromatin packing regulate the cell cycle?", Physiol Genomics 46 (6): 191-194 (2014).

Coller, H.A., "Is cancer a metabolic disease?", American Journal of Pathology 184 (1): 4-17 (2014).

Evertts, A.G., Wang, X., Manning, A.L., Dyson, N.J., Garcia, B.A., and Coller, H.A., "H4K20 methylation functions in quiescence and chromatin compaction", Molecular Biology of the Cell 24 (19): 3025-3037 (2014).

Jiang P, Singh M, Coller HA., "Computational assessment of the cooperativity between RNA binding proteins and MicroRNAs in Transcript Decay", PLoS Comput Biol 9 (5): (2013). [link]

Coller, H., "Introducing the systems biology of cell state", Physiological Genomics 45 (11): 407-408 (2013).

Evertts, A., Zee, B.M., DiMaggio, P.A., Gonzales-Cope, M., Coller, H.A. and Garcia, B.A., "Quantitative dynamics of the link between cellular metabolism and histone acetylation", Journal of Biological Chemistry 288 (17): (2013).

Klionsky et al., "Guidelines for the use and interpretation of assays for monitoring autophagy", Autophagy 8 (4): 445-544 (2013).

Sang, L. and Coller, H.A., "Fear of commitment: Hes1 protects quiescent fibroblasts from irreversible cellular fates", Cell Cycle 8 (14): 2161-2167 (2013).

Coller, H.A. and Kruglyak, L., "It's the sequence, stupid!", Science 322 (5900): 380-381 (2013).

Evertts AG, Coller HA., "Back to the origin: reconsidering replication, transcription, epigenetics, and cell cycle control", Genes Cancer 3 (11-12): 678-696 (2012). [link]

Suh, E.J., Remillard, M.Y., Legesse-Miller, A., Johnson, E.L. Lemons, J.M.S., Chapman, T.R., Forman, J.J., Kojima, M., Silberman, E.S., and Coller, H.A., "A microRNA network regulates proliferative timing and extracellular matrix synthesis during cellular quiescence in fibroblasts", Genome Biology 13 (12): (2012).

Legesse-Miller, A., Raitman, I., Haley, E.M., Liao, A., Sun, L., Wang, D.J., Suh, E.J., Johnson, E.L., Lund, B., and Coller, H.A., "Quiescent fibroblasts are protected from proteasome inhibition-mediated toxicity", Molecular Biology of the Cell 23 (18): 3566-3581 (2012).