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. 2006 Dec;174(4):1745–1754. doi: 10.1534/genetics.106.058933

Figure 3.—

Figure 3.—

SPO11-HA suppresses sgs1795. (A) Configuration of markers in strains used for analysis of crossing over in various mutant backgrounds. (B) COs were measured in four intervals in wild type (BR4316), sgs1795 (BR4474), spo11-HA (BR4357), and sgs1795 spo11-HA (BR4475). Intervals are designated by the color utilized in A. Asterisks denote intervals in which map distances are significantly different from those in sgs1 (P < 0.05). (C) Spread nucleus from sgs1795 cell at pachytene stained for Zip3-GFP (green) and Zip1 (red) in pachytene. Yellow indicates regions of overlap. Bar, 1 μm. (D) Spread nucleus from sgs1795 spo11-HA stained as in C. Bar, 1 μm. (E) Zip3-GFP foci were quantified in pachytene-staged chromosome spreads. Asterisks denote strains in which the number of Zip3 foci is significantly different from that of sgs1795 (P < 0.05 using the t-test). (F) Spore viability. Differences between strains were assessed using the big G-test with spore viability patterns (i.e., four-, three-, two-, one-, and zero-spore viable, not shown). Asterisks denote strains in which spore viability is significantly different from that of sgs1795.