Schizosaccharomyces pombe RanGAP Homolog, SpRna1, Is Required for Centromeric Silencing and Chromosome Segregation
Mol. Biol. Cell Kusano et al.
15: 4960
Supplemental Figures
This article contains the following supporting material:
Supplemental Figure 1.pdf -
Swi6-GFP localization in Sprna1ts mutants.
Cultures of indicated cells were incubated at 26°C and then half of cultures were incubated at 37°C for 4 hours. Images of wild-type, Sprna1-86ts and Sprna1-87ts were shown as representatives. The localization of Swi6 was detected with GFP-fused Swi6 (gift from Dr. Y. Watanabe, Univ. of Tokyo) that was integrated into the genome. DNA was stained with DAPI (blue). Left columns showed the localization of GFP and right columns showed a merged image with DAPI (blue) at the indicated temperature. Scale bar, 5 μm.
Supplemental Figure 2.pdf -
Gene silencing activity of Sprna1ts mutants expressing clr4+. Sprna1ts [imr1R::ura4+] strains expressing clr4+ were spotted. The h+975 and h+ura4-D18 were used as the control strains of either Ura4+ or Ura4- cells, respectively. The dotted marks of these strains, indicated that they have no plasmids. Each strain was grown to 1.0 x 107 cells/ml in YE5S. Serial dilution (1:5) of the indicated cultures were spotted onto non-selective (N/S), selective (Ura-), or counterselective (5FOA) plates and incubated at 30°C for five days. The highest density spots contained 1 x 104 cells.