Supplemental Material for Ohkuni et al., 2020

<b>Table S1. </b><i>S. cerevisiae</i> strains used in this study.<b>Table S2.</b> Plasmids used in this study.<b>Table S3.</b> Primers used in this study.<b>Figure S1. </b>The stability of HA-Cse4 K215/216R/A is not increased when compared to HA-Cse4 in a <i>psh1</i>∆ strain. <b>Figure S2. </b>Levels of chromatin associated Cse4 K215/216R/A are reduced when compared to wild-type Cse4.<b>Figure S3. </b>Protein levels of Cse4 and Cse4 K215/216R under the copper-inducible promoter.<b>Figure S4. </b><i>GAL-cse4 K65R</i> exhibits SDL in <i>slx5</i>∆ and <i>hir2</i>∆ strains and those are suppressed by <i>cse4 K215/216R</i>.