Clarke D J, Segal M, Jensen S, Reed S I
Department of Molecular Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.
Nat Cell Biol. 2001 Jul;3(7):619-27. doi: 10.1038/35083009.
Genetic evidence suggests that the securin Pds1p is the target of a late-S-phase checkpoint control. Here we show that Pds1p becomes essential once two-thirds of the genome has been replicated and that the coupling of the completion of genome replication with mitosis relies on the regulation of Pds1p levels. Mec1p is needed to maintain Pds1p levels under S-phase checkpoint conditions. In contrast, Rad53p and Chk1p, needed for the stabilization of Pds1p in the context of the G2 DNA-damage checkpoint pathway, are dispensable. Thus, the Pds1p-dependent late-S-phase checkpoint pathway couples replication with mitosis but is mechanistically distinct from the G2 DNA-damage checkpoint. Finally, we show that the inhibition of spindle elongation in early S phase, controlled by the Mec1p/Rad53p branch, is not regulated via Pds1p/Esp1p. This can mechanistically explain the need for branched S-phase checkpoint controls.
遗传学证据表明,分裂后期促进因子Pds1p是S期后期关卡调控的靶点。我们在此表明,一旦基因组的三分之二完成复制,Pds1p就变得至关重要,并且基因组复制的完成与有丝分裂的耦合依赖于Pds1p水平的调控。在S期关卡条件下,需要Mec1p来维持Pds1p的水平。相比之下,在G2期DNA损伤关卡途径中稳定Pds1p所需的Rad53p和Chk1p则是可有可无的。因此,依赖Pds1p的S期后期关卡途径将复制与有丝分裂耦合在一起,但在机制上与G2期DNA损伤关卡不同。最后,我们表明,由Mec1p/Rad53p分支控制的S期早期纺锤体伸长的抑制并不通过Pds1p/Esp1p进行调控。这在机制上可以解释对分支S期关卡调控的需求。