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. 2013 Sep 26;42(1):417–429. doi: 10.1093/nar/gkt856

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© The Author(s) 2013. Published by Oxford University Press.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 7. — Transcript levels of miRNA processing proteins, pre-miRs, miRNAs and target genes measured by RT-qPCR in different algal materials. (A) AGO1 and DCL1 cDNAs. (B) Pre-miRs detected in Figure 4. The data are expressed as fold changes relative to the control. ‘Control’: sporophytes grown in normal culture conditions, used to set the reference value at 1; ‘Gametophyte’: gametophytes grown in normal culture conditions; ‘Hypo-saline’ and ‘Hyper-saline’: sporophytes subjected to corresponding osmotic stress conditions. Conditions for which the distribution of replicates values significantly differs from the control distribution (Student t-test, α = 0.05) are denoted by an asterisk.