Cancer Research UK

Our other websites:

London Research Institute

Martin Singleton : Macromolecular Structure and Function

Goals

Our lab is interested in understanding how chromosomes, once replicated, are separated into daughter cells during cell division. It is essential the this process works accurately over many generations, otherwise cells may gain or loose chromosomes, an event that can have severe consequences for the cell, and in turn lead to the onset or progression of diseases such as cancer. We primarily study these processes by determining the three-dimensional structure of proteins that bind chromosomes using techniques such as X-ray crystallography and electron microscopy. By designing experiments based on the resulting structures, we can gain insights into the way in which the proteins operate in the cell.

Selected Papers

Perriches T, Singleton MR. The structure of the yeast kinetochore Ndc10 DNA-binding domain reveals an unexpected evolutionary relationship to tyrosine recombinases. J Biol Chem. 2012;287(7):5173-5179 (Abstract)
Zhang G, Kelstrup CD, Hu XW, Hansen MJ, Singleton MR, Olsen JV, Nilsson J. The Ndc80 internal loop is required for recruitment of the Ska complex to establish end-on microtubule attachment to kinetochores. J Cell Sci. 2012 Mar 27. [Epub ahead of print] (Abstract)
Kingston IJ, Yung JS, Singleton MR. Biophysical Characterization of the Centromere-specific Nucleosome from Budding Yeast. J Biol Chem. 2011;286(5):4021-6 (Abstract)
Maskell DP, Hu XW, Singleton MR. Molecular architecture and assembly of the yeast kinetochore MIND complex. J Cell Biol. 2010;190(5):823-34 (Abstract)
Purvis A, Singleton MR. Insights into kinetochore-DNA interactions from the structure of Cep3∆. EMBO Reps. 2008;9:56-62 (Abstract)
Singleton MR, Dillingham MS, Gaudier M, Kowalczykowski SC, Wigley DB. Crystal structure of RecBCD enzyme reveals a machine for processing DNA breaks. Nature. 2004;432:187-193 (Abstract)