Cohesins Functionally Associate with CTCF on Mammalian Chromosome Arms

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• Dr Suzana Hadjur, MRC Clinical Science Center, Imperial College, London, UK (Host: M. Madan Babu)
• Wednesday 04 June 2008, 14:00-15:00
• Structural Studies Coffee room, MRC Laboratory of Molecular Biology.

If you have a question about this talk, please contact Duncan Simpson.

Cohesins mediate sister chromatid cohesion, which is essential for chromosome segregation and postreplicative DNA repair. In addition, cohesins appear to regulate gene expression and enhancer-promoter interactions. These noncanonical functions remained unexplained because knowledge of cohesin-binding sites and functional interactors in metazoans was lacking. We show that the distribution of cohesins on mammalian chromosome arms is not driven by transcriptional activity. Instead, mammalian cohesins occupy a subset of DNase I hypersensitive sites, many of which contain sequence motifs resembling the consensus for CTCF , a DNA -binding protein with enhancer blocking function and boundary element activity. We find cohesins at most CTCF sites and show that CTCF is required for cohesin localization to these sites. Recruitment by CTCF suggests a rationale for noncanonical cohesin functions and, because CTCF binding is sensitive to DNA methylation, allows cohesin positioning to integrate DNA sequnce and epigenetic state.

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