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  Cytoskeletal organisation and cell signaling responses to stress


   School of Biological Sciences

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  Prof K E Sawin  No more applications being accepted  Competition Funded PhD Project (Students Worldwide)

About the Project

Interested individuals must follow Steps 1, 2 and 3 at this link on how to apply
http://www.ed.ac.uk/biology/prospective-students/postgraduate/pgr/how-to-apply


In order to maintain their stereotypic organisation, cells must be able to respond to internal cues and also coordinate responses to external stresses to achieve homeostasis at the level of the entire cell. Our laboratory studies eukaryotic cellular organisation, with a particular focus on the microtubule and actin cytoskeleton systems and cell polarity regulation. We use the unicellular fission yeast Schizosaccharomyces pombe as a model organism, because of its decreased complexity relative to mammalian cells, as well as its amenability to combined genetics, microscopy, and biochemistry approaches.

Recently we have discovered an unexpected close link between stress-activated protein kinase signaling and cell polarity (Mutavchiev et al., in press). Because of the intimate associations between cell polarity regulators and the cytoskeleton, we are interested in investigating how activation of stress pathways affects regulation of the cytoskeleton. The PhD project will follow an interdisciplinary approach to this question, to identify molecular controls on the cytoskeleton via stress signaling.

Methods used in the PhD project would include: classical and molecular genetics (including genome engineering); live-cell microscopy using fluorescent-tagged proteins (this is one of our strengths—there are several different state-of-the art microscopes in our facility); and biochemistry and mass spectrometry/proteomic methods. PhD projects involving yeast genetics and cell biology are a great way to begin a scientific research career, because a wealth of methods are learned and applied in the context of hypothesis-driven research, and hypotheses are constantly challenged by new results requiring rigorous logical evaluation.

We are a vibrant and international group of PhD students and postdocs. For further information about the laboratory, visit http://sawin.bio.ed.ac.uk/ , http://www.wcb.ed.ac.uk/research/sawin

Funding Notes

Please follow the instructions on how to apply http://www.ed.ac.uk/biology/prospective-students/postgraduate/pgr/how-to-apply

If you would like us to consider you for one of our scholarships you must apply by 12 noon on Monday 5th January 2018 at the latest.

References

Mutavchiev, D.R., Leda, M., and Sawin, K.E. (2016). Remodeling of the Fission Yeast Cdc42 Cell-Polarity Module via the Sty1 p38 Stress-Activated Protein Kinase Pathway. Curr Biol 26, 2921-2928. http://doi.org/10.1016/j.cub.2016.08.048

Borek, W. E., Groocock, L. M., Samejima, I., Zou, J., de Lima Alves, F., Rappsilber, J., & Sawin, K. E. (2015). Mto2 multisite phosphorylation inactivates non-spindle microtubule nucleation complexes during mitosis. Nature Communications 6, 7929. http://doi.org/10.1038/ncomms8929

Lynch, E. M., Groocock, L. M., Borek, W. E., & Sawin, K. E. (2014). Activation of the γ-Tubulin Complex by the Mto1/2 Complex. Current Biology 24, 896–903. http://doi.org/10.1016/j.cub.2014.03.006

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