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. 2015 Jun 15;11(6):e1005281. doi: 10.1371/journal.pgen.1005281

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© 2015 Xu 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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Fig 6 — qPCR results are shown for TER1 and TER2/TER2Δ from Col-0 and Ler-0 in the presence of cordycepin. Col-0 and Ler-0 seedlings were treated with cordycepin (100μg/μl) for the times indicated followed by qPCR to monitor TER1 (A) and TER2/ TER2Δ (B). The values obtained for untreated RNA samples were set to 0 and the fold decrease is shown. eIF-4a was used as reference gene for normalization. (C-E) qPCR results from a time course experiment of Col-0 seedlings treated with cordycepin followed by zeocin. Seedlings were incubated with cordycepin for 1.5 h to shut down transcription, and zeocin was added (red arrows). The incubation continued for a total of 3.5 h. Results for BRCA1 (C), TER1 (D), TER2 (E) are shown.