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Cohesion between sister chromatids depends on a multiprotein complex called cohesin that has been proposed to hold sister DNAs together by trapping them inside a large tripartite ring. Sister chromatid cohesion has hitherto only been detected by using cytological methods in living cells. We show here that cohesion between the sister DNAs of circular minichromosomes established in vivo can be detected in vitro by velocity gradient sedimentation and agarose-gel electrophoresis. This ex vivo cohesion does not depend on intercatenation of sister DNAs but is destroyed by cleavage of cohesin's Scc1 subunit or minichromosome linearization. These data represent the best evidence so far that the cohesin ring physically holds sister DNAs together and are consistent with the notion that it does so by using a topological principle involving the trapping DNAs inside its ring.

Original publication




Journal article


Mol Cell

Publication Date





300 - 310


Acetyltransferases, Adhesiveness, Cell Cycle, Cell Cycle Proteins, Chromatids, Chromosomal Proteins, Non-Histone, DNA, Circular, DNA, Fungal, Models, Biological, Nuclear Proteins, Phosphoproteins, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Sister Chromatid Exchange