Fig. 6
- ID
- ZDB-FIG-170921-56
- Publication
- Gallagher et al., 2017 - Pnrc2 regulates 3'UTR-mediated decay of segmentation clock-associated transcripts during zebrafish segmentation
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pnrc2 and the nonsense-mediated decay effector Upf1 promote decay of cyclic mRNA. Injection of low dose pnrc2 sbMO (2 ng) has little to no effect on her1 expression (A, C), contrasting with the expected her1 misexpression observed after injection of moderate dose pnrc2 sbMO (6 ng) (B). Low dose injection of upf1 sbMO (0.25 ng) also has little effect on her1 expression (D), but when combined with a low dose of pnrc2 sbMO (2 ng), her1 misexpression is observed in about 50% of injected embryos (E). The proportion affected in each condition is plotted on a bar graph that indicates significant differences between single morphants, double morphants, and controls (F). sbMO = splice-blocking MO; **** = p<0.0001. |
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Stage: | 14-19 somites |
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Stage: | 14-19 somites |
Reprinted from Developmental Biology, 429(1), Gallagher, T.L., Tietz, K.T., Morrow, Z.T., McCammon, J.M., Goldrich, M.L., Derr, N.L., Amacher, S.L., Pnrc2 regulates 3'UTR-mediated decay of segmentation clock-associated transcripts during zebrafish segmentation, 225-239, Copyright (2017) with permission from Elsevier. Full text @ Dev. Biol.