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. 2018 Aug 1;32(15-16):1060–1074. doi: 10.1101/gad.316034.118

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© 2018 Lee et al.; Published by Cold Spring Harbor Laboratory Press

This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six 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 4. — hnRNPA1 differentially spliced transcripts with nuclear eCLIP peaks in human K562 cells. (A) Venn diagram showing the overlap between the differential splicing target RNAs and nuclear hnRNPA1-binding targets in K562 cells. (B) A list of common differential splicing targets from JUM and MISO analysis that contain nuclear hnRNPA1 eCLIP targets. (C) GO enrichment of hnRNPA1 targets containing nuclear eCLIP tags revealed that these target RNAs are involved in processes such as protein localization to the ER, the mRNA metabolic process, translational initiation, and nonsense-mediated decay.