That poses an obvious problem during S phase: While DNA replication machineries («replisomes») zip along the chromosomes trying to faithfully duplicate the entire genome in a matter of just a couple of hours, they encounter — on average — multiple
cohesin rings that are already wrapped around DNA.
The last stage in the life of
a cohesin ring is its removal from centromeres, a tightly regulated process, which involves proteolytic cleavage of cohesin's Scc1 / Rad21 subunit (see Figure 2).
Not exact matches
Cohesin encircles the DNA strand as a
ring does around a piece of string, and the protein complexes that replicate DNA can pass through the
ring without displacing it.
Since the two new DNA strands are caught in the
ring, only one
cohesin is needed to mark the two, thereby helping the transcription factors to find their original binding region on both DNA strands.
There is good evidence that initial
cohesin loading is already topological (meaning, the
ring closes around the single chromatid).
And while we're still far away from completely understanding this complex complex, we already know enough to say that
cohesin really is «one
ring to rule them all».
And while this feat should already be enough to warrant devoting a whole blog post to
cohesin, you will shortly realize that this complex also performs a myriad of other functions during the cell cycle, which really makes it «one
ring to rule them all».