“Science never solves a problem without creating ten more.” — George Bernard Shaw
Evolution and Formation of Protein Complexes
Ph.D. – University of California, Los Angeles, 2015
B.S. – Creighton University, 2008
2500 California Plaza
Omaha, NE 68178-0103
Additional website: https://cavanaughlab.wordpress.com
- BIO 362 – Cell Structure and Function
In the Cavanaugh lab we use two related species of yeast, S. cerevisiae, and K. lactis, to study the organization, dynamics, and evolution of the spindle pole body (SPB). The SPB is a microtubule organizing center and serves to organize and regulate the formation of the mitotic spindle in yeast. Although the function of the SPB is vitally important for yeast reproduction, the structure and composition of this large, multi-protein structure varies widely across the yeast phyla. By studying the SPB in two species of budding yeast we hope to uncover mechanisms by which individual proteins are able to co-evolve as part of a large protein structure.
Cavanaugh, A. M. and S. L. Jaspersen. 2017. Big lessons from little yeast: Budding and fission yeast Centrosome Structure, Duplication, and Function. Annual Reviews Genetics. 51: 361-383.
Cavanaugh, A. M., J. Huang, J.-N. Chen. 2015. Two developmentally distinct populations of neural crest cells contribute to the zebrafish heart. Developmental Biology2): 103-112.
Patterson, R. A., A. M. Cavanaugh, V. Cantemir, P. R. Brauer, M. V. Reedy. 2013. MT2-MMP expression during early avian morphogenesis. The Anatomical Record. 296(1): 64-70.
Langenbacher, A. D., C. T. Nguyen, A. M. Cavanaugh, J. Huang, F. Lu, J.-N. Chen. 2011. The PAF1 complex differentially regulates cardiomyocyte specification. Developmental Biology. 353: 19-28.
O’Brien, G. S., S. Rieger, S. M. Martin, A. M. Cavanaugh, C. Portera-Cailliau, A. Sagasti. 2009. Two-photon axotomy and time-lapse confocal imaging in live zebrafish embryos. Journal of Visualized Experiments. 24: 1129.