The Conserved Spc7 Protein Is Required for Spindle Integrity and Links Kinetochore Complexes in Fission Yeast
Mol. Biol. Cell Kerres et al.
18: 2441
Supplemental Material
This article contains the following supporting material:
Supplemental Figure 1
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(A) Diagrammatic representation of the genetic interactions between spc7+ and nuf2+ and mis12+. (B) Serial dilution patch tests (104 to 101 cells) of spc7-23, mis12-537 and a spc7-23 mis12-537 double mutant grown on YE5S for 4 (25°C) or 3 (28°C) days. (C) and (D) Serial dilution patch tests (104 to 101 cells) of nuf2-1 and mis12-537 strains overexpressing spc7+ or spc7-23 cells expressing extra mis12+. Transformants were grown under selective conditions at the indicated temperatures for 5 to 7 days. v indicates vector control; spc7+ denotes the presence of wild-type spc7+ driven by the nmt41 promoter under derepressed conditions.
Supplemental Figure 2
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Chromosome segregation and spindle phenotypes observed in spc7-30 and spc7-30nmt81-GFP-atb2 strains incubated at 34°C. Spindle phenotypes from left to right: wild-type anaphase spindle, anaphase spindles with a thinly staining midzone, disintegrating/broken anaphase spindles, bent spindles and unequally stained spindles. N/strain= 100.