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. 2016 Mar;22(3):416–427. doi: 10.1261/rna.055178.115

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© 2016 Ruminski et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society

This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.

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FIGURE 3. — Mss116p did not affect chimeric mRNA stability or self-cleavage activity nonspecifically in yeast. (A) Secondary structure of HP210, which does not contain a complementary insert with the potential to form an alternative helix. Chimeric HP210 mRNAs were coexpressed in yeast with (B) active Mss116p (Δmts), (C) catalytically inactive Mss116p (ΔmtsE268Q), or (D) empty vector. Plots display results from a representative pair of experiments with functional (▪) and mutationally inactivated (□) chimeric HP210 mRNAs. Reported values represent the mean and standard deviation obtained from two or more pairs of experiments.