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Cell Cycle Group home page

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Sun sets on the CSC [+]
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Sun sets on the CSC
Welcome to the Cell Cycle Group web site. The laboratory, led by Luis Aragón, was established in 2002 and is part of the Epigenetics, Development and Cancer Section of the MRC Clinical Sciences Centre and Imperial College London. The Group is a talented and friendly team comprising postdoctoral fellows, PhD students and a research assistant who use budding yeast as a model system to investigate fundamental questions in biology. In these pages you will find information about the Group and its research, as well as research opportunities in the laboratory. We encourage you to contact us if you have any questions about the Group or this site.

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Yeast cells [+]
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Wild type yeast cells in metaphase. Cells express the nucleolar marker Net1 fused to the green fluorescent protein (GFP). Cells were arrested in metaphase using the microtubule inhibitor nocodazole. The nuclei are shown in red and the ribosomal DNA in green. Note how the rDNA located in the middle of the large chromosome XII protrudes from the main nuclear body forming a loop.
 
The objective of the Cell Cycle Group is to understand the molecular mechanisms orchestrating the equal and faithful segregation of chromosomes during cellular division. Cells have an extraordinary ability to replicate; this property makes them the most complex entities known and is the essence of life itself. The thrill of studying the cell cycle is touching fundamental processes of life while dealing with very sophisticated mechanisms. Cells inherit their genetic information in the form of chromosomes during mitosis from a mother cell. Following DNA replication in S-phase, cells are linked together (sister-chromatid cohesion), compacted (chromosome condensation), untangled and then moved to opposite poles of the cell (segregation). All these events are coordinated and executed with astonishing precision to prevent aneuploidy, a condition of inappropriate chromosome number that is associated with the development of malignant cancer and birth defects.

The work of the group is focused on the analysis of protein complexes that mediate chromosome structure and segregation, namely cohesin, condensin and a novel complex, the 'SMC5/SMC6'. We are also interested in regulatory networks that operate during cellular divisions. We use yeast as a model organism in our efforts to unravel the controls that govern chromosome segregation and cell cycle progression.