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The propagation of our genomes during cell proliferation depends on the movement of sister DNA molecules produced by DNA replication to opposite sides of the cell before it divides. This feat is achieved by microtubules in eukaryotic cells but it has long remained a mystery how cells ensure that sister DNAs attach to microtubules with opposite orientations, known as amphitelic attachment. It is currently thought that sister chromatid cohesion has a crucial role. By resisting the forces exerted by microtubules, sister chromatid cohesion gives rise to tension that is thought essential for stabilizing kinetochore-microtubule attachments. Efficient amphitelic attachment is therefore achieved by an error correction mechanism that selectively eliminates connections that do not give rise to tension. Cohesion between sister chromatids is mediated by a multisubunit complex called cohesin which forms a gigantic ring structure. It has been proposed that sister DNAs are held together owing to their becoming entrapped within a single cohesin ring. Cohesion between sister chromatids is destroyed at the metaphase to anaphase transition by proteolytic cleavage of cohesin's Scc1 subunit by a thiol protease called separase, which severs the ring and thereby releases sister DNAs.

Original publication

DOI

10.1098/rstb.2003.1417

Type

Journal article

Journal

Philos Trans R Soc Lond B Biol Sci

Publication Date

29/01/2004

Volume

359

Pages

99 - 108

Keywords

Cell Cycle Proteins, Chromatids, Chromosomal Proteins, Non-Histone, Chromosome Segregation, DNA, DNA Replication, Endopeptidases, Fungal Proteins, Microtubules, Models, Genetic, Nuclear Proteins, Separase