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. 2015 May 4;10(5):e0125358. doi: 10.1371/journal.pone.0125358

Fig 7. End joining activity of Chimera 1 consisting of PfalMre11 nuclease domain in conjunction with the DDR domain of ScMre11.

Fig 7

(A) The relevant genotype of each strain is marked on the X-axis. The schematic diagram of the plasmid used for this assay is shown in the inset. The end joining assays were performed as described in the Method section. (B) PfalMre11 is capable of interacting with YKu80. Yeast-two- hybrid analysis between YKu80 cloned into the bait vector (pGBDUC1) vector and PfalMre11 or Chimera 1 cloned into the prey vector (pGADC1). ScMre11 acted as a positive control. The P value was calculated by two-tailed Student’s t-test (* indicates P <0.05, N.S. means not significant).