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. 2013 Jan 17;9(1):e1003197. doi: 10.1371/journal.pgen.1003197

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© 2013 Lui et al

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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Kinetics of pairing in cells with tetO arrays integrated at URA3, located 35 kb away from the centromere on chromosome V, and expressing tetR-GFP fusion protein. Homologs are considered paired if only one GFP can be visualized in the cells (n = 200) from each time point. Error bars represent the standard error of the percentage of cells paired for independent cultures for each mutant (n = 200). All strains carry the ndt80Δ mutation. A. Analysis of WT (center panel and left panel) and ndj1Δ (right panel and left panel) pairing kinetics in the presence or absence of Lat B. B. Analysis of csm4Δ (center panel and left panel) and ndj1Δ csm4Δ (right panel and left panel) pairing kinetics in the presence or absence of Lat B.