Hen the speed of replication forks modifications,this impacts the programming of origin firing inside the subsequent cell cycle (Courbet et alin which replication factories might signal a change of the fork speed.embedded in the nuclear envelope,which remains intact throughout the cell cycle (closed mitosis; Heath,and kinetochores are tethered to SPBs by microtubules through most of the cell cycle. Nevertheless,it was revealed that,upon centromere DNA replication,kinetochores are transiently disassembled,causing centromere detachment from microtubules for min (Kitamura et al Subsequently kinetochores are reassembled and interact with microtubules once more. Because centromeres are replicated in early S phase in budding yeast (McCarroll and Fangman ; Raghuraman et alcentromere detachment and reattachment also happen in early S phase. The timing of these events is presumably crucial to make a time window sufficient (even within the absence of G phase; see below) for establishment of suitable kinetochoremicrotubule attachment,before chromosome segregation in subsequent anaphase. Telomeres in budding yeast have a tendency to localize at the nuclear periphery from the end of mitosis to G phase,and this localization depends on the Ku and Sirmediated anchoring mechanisms (Hediger et al. ; Taddei and Gasser. Prior to anaphase,even so,telomeres localize randomly within the nucleus (Laroche et al. ; Hediger et al It was demonstrated that the delocalization of telomeres from the nuclear periphery is triggered by their DNA replication,which suppresses the Kumediated anchoring mechanism in late S phase (Ebrahimi and Donaldson. The detachment of telomeres in the nuclear periphery likely enhances telomere mobility within the nucleus,which has an benefit in subsequent chromosome segregation. As a result,replication at centromeres and telomeres is closely linked to chromosome segregation in mitosis. This link is in all probability vital in budding yeast since it is thought that S phase and mitosis are overlapped,and G phase is absent in this organism (Kitamura et alConclusions and perspectives DNA replication at centromeres and telomeres In this section,we briefly discuss DNA replication at centromeres and telomeres as examples of spatial regulation of replication in particular chromosome contexts. In budding yeast,spindle pole bodies (SPBs; microtubuleorganizing centers in yeast) are DNA replication is actually a spatially regulated procedure at many levels; i.e from replisome architecture to subnuclear chromosome organization. The spatial regulation of DNA replication is closely linked to its temporal regulation. Both spatial and temporal regulations look to become significant for effective duplication of chromosomes,for correct responses to replicationSpatial organization of DNA replication Bates D,Kleckner N Chromosome and replisome dynamics PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/28497198 in E. coli: loss of sister cohesion triggers global chromosome movement and mediates chromosome segregation. J Cell Biol : Dingman CW Bidirectional chromosome replication: some topological considerations.MacAlpine et al Singlecell and singlemolecule assays have enabled analyses of DNA replication in higher spatial and temporal resolution and have opened a window into how DNA replication differs from cell to cell and from chromosome to chromosome (P7C3 price Michalet et al. ; Herrick et al. ; Kitamura et al Additional improvement of these methods along with other biochemical,genetic,and cell biological approaches will advance additional the study of chromosome duplication.Acknowledgments We thank Julian.