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. 2021 Jan 12;12(1):74. doi: 10.1038/s41419-020-03360-6

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© The Author(s) 2021

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 5 — A RIP-seq of SW480/DDX39B showed that DDX39B binds directly to multiple sites of FUT3 pre-mRNA (red box: a partial sequence of the exon1, validated by RIP). B The DDX39B-binding motif, presented by RIP-seq. C DDX39B binds the first exon of FUT3 mRNA, validated by RIP (red box in (A)); error bars, SD. D DDX39B interacting with FUT3 as a part of EJC/TREX complex, shown using STRING. E Fold change of FUT3 mRNA expression in SW480 cells with DDX39B overexpression and silencing (nuclear and cytoplasmic separation assay); error bars, SD. F Minigene assay showed the splicing effect of DDX39B on FUT3 pre-mRNA.