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. 2016 Mar 29;67(9):2745–2760. doi: 10.1093/jxb/erw107

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© The Author 2016. Published by Oxford University Press on behalf of the Society for Experimental Biology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 8. — SnRK1.1 regulated the MPK6 signalling pathway under submergence. (A) Phosphorylation of MPK3 and MPK6 in Col-0 and SnRK1.1 ^K48M-5 under submergence. The data represent three independent biological replicates. TUBULIN was used as an internal control. (B) Expression of MPK signalling marker genes in Col-0, SnRK1.1 ^K48M, and mpk6. Transcript levels were detected by qRT-PCR by specific primers. TUBULIN mRNA was the internal control. The data represent means ±SD from four independent biological replicates. Statistical differences between Col-0 and the mutants were determined by Student’s t test. *, P <0.05.