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. 2017 May 31;13(5):e1006827. doi: 10.1371/journal.pgen.1006827

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© 2017 Su 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 credited.

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Fig 3 — (A) Yeast two-hybrid assay showing AtXRCC3 interaction with AtRAD51 and AtRAD51C. The known DYT1-DYT1 interaction is used as a positive control [82]. AD refers to the activation domain, BD refers to the DNA-binding domain, SD-2 refers to SD-Leu-Trp and SD-4 refers to SD-Leu-Trp-His-Ade+X-gal. Blue indicates a positive interaction. (B) Pull-down assay showing that AtRAD51C interacts with AtRAD51 and AtXRCC3. (C) BiFC assay in tobacco cells showing strong nuclear signals for AtRAD51-AtRAD51C and AtRAD51C-AtXRCC3 interactions. Left panels are yellow fluorescent protein (YFP) signals, middle panels are nuclei stained with 6-diamidino-2-phenylindole (DAPI), and right panels merge the DAPI-stained images with the YFP signals and bright field images.