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. 2023 Mar 22;20(1):85–94. doi: 10.1080/15476286.2023.2192553

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© 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.

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Figure 4. — A) Schematic representation of hnRNP A2/B1 and the GFP-A2/B1 protein construct. B) Translational repression assay results for RNA reporters H1-H3 in the presence of GFP-A2/B1 in comparison with RNA reporter S6 in the presence of GFP-SRSF1 C) Correlation between TagBFP production rate and the distance between a secondary structure and the SD sequence for GFP-A2/B1 (top) and GFP-SRSF1 (bottom). D) Predicted secondary structures of the inserted RBP binding sequences for 5’-UTRs of the reporters S6 and H1-H3 using RNAfold. The first three nucleotides of the SD sequence are indicated as well as the distance between the SD and the closest predicted secondary structure.