FIGURE 1:
alp16Δ is synthetic lethal with the mzt1-T27W mutant, and Alp16GCP6 localizes to mitotic SPBs in the absence of Gfh1GCP4 and Mod21GCP5. (A) alp16Δ is synthetic lethal with the mzt1-T27W mutant. Diploid cells obtained from crosses between mzt1-T27W-hphR and gfh1Δ-kanR, mod21Δ-kanR, or alp16Δ-kanR were sporulated, and individual spores (a–d) in each ascus (1–5) were dissected on YES plates. Nonviable spores from the cross between mzt1-T27W and alp16Δ germinated, divided several times, and arrested with elongated morphologies. Drug resistance of viable spores (orange circle) and predicted resistance of nonviable spores (white circle): k, kanR (resistance to G418); h, hphR (resistance to hygromycin B). (B) Localization of Alp16GCP6, Gfh1GCP4, and Mod21GCP5 to mitotic SPBs. Localization of GFP-Alp16GCP6, GFP-Gfh1GCP4, and GFP-Mod21GCP5 to mitotic SPBs was examined in wild-type (WT), gfh1Δ, mod21Δ, and alp16Δ cells containing mCh-Atb2 and Sid4-mRFP. Scale bar, 10 μm.