ck of Haspin kinases ought not to enhance the Ipl1 inner-centromere localization defect seen in top2 mutants. Corroborating the biochemical analysis, we observed that top2-4 alk1 alk2 and top2CTD alk1 alk2 mutants were no more defective in Ipl1 localization than the single top2 mutants, 658 JCB Volume 213 HC-030031 chemical information NumBer 6 2016 If the role of Topo II in Ipl1 inner-centromere recruitment is to promote H3 T3 phosphorylation by Haspin, then a phosphomimetic H3 T3 residue would be predicted to bypass the requirement for Topo II in this mechanism. To test this, we first asked if expression of wild-type H3 can restore Ipl1 innercentromere localization in the h3-T3A mutant to provide a baseline measurement of rescue efficiency. The temporal parameters for this experiment were important to establish because expression of wild-type H3 would allow only a gradual displacement of mutant h3-T3A histone from the genome and from inner centromeres. In time course experiments, after induction of wild-type H3 expression from the GAL10 promoter, a peak of rescued Ipl1 inner-centromere localization at metaphase was observed after 2 h. Given that this is approximately the length of one cell cycle, PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/19835934 during which not more than half 
of the mutant H3 is expected to be replaced as a consequence of DNA replication, the rescue of Ipl1 localization to 40% of cells is striking. At 4 h after induction, we observed that the cells had large vacuoles, consistent with previous studies that overexpression of H3 is detrimental to growth. These data therefore establish the window of time that is optimal for assessing rescue of Ipl1 inner-centromere localization in metaphase. We next asked if expression of a phosphomimetic h3-T3E histone is able to alleviate the Haspin kinase and Topo II requirements for Ipl1 inner-centromere recruitment in mitosis. As predicted, if Haspin kinases are required for H3 T3 phosphorylation in S. cerevisiae, Ipl1 inner-centromere localization in mitosis was partly restored by h3-T3E histone in alk1 alk2 mutant cells. Importantly, when expressed in the top2CTD mutant, bypass of the requirement for the CTD was also observed, with Ipl1 localizing correctly in 47% of cells 2 h after induction of the h3-T3E mutant. These data provide evidence directly linking the yeast Topo II CTD to Haspin-mediated H3 T3 phosphorylation, required for Ipl1 recruitment to inner centromeres in metaphase. We conclude that the centromere function of the Topo II CTD is to recruit Ipl1 via the HaspinH3 T3-Phos pathway. Discussion The SPR of Topo II has been studied extensively using biochemical and structural approaches because it is the target of several important classes of antitumor drugs. However, binding of Topo II to DNA occurs even in the absence of the catalytic activity of the enzyme, and it has remained unknown whether Topo II plays additional roles in cells that are not associated with the DNA topology changes induced by the SPR. In particular, an important region of the enzyme is the CTD, which is dispensable for the SPR but is nevertheless required for faithful chromosome segregation from yeast to human cells Representative images and quantification of Ipl1-GFP localization to inner centromeres in prometaphase/metaphase alk1 alk2, h3-T3A, top2-4 alk1 alk2, and top2CTD alk1 alk2. Spc110-mCherry indicates spindle poles. Bars, 1 m. n is the total number of cells scored from three experimental repeats. H3 phosphorylated at threonine 3 was quantified relative to loading contr
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