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. 2016 Oct 28;17:845. doi: 10.1186/s12864-016-3172-6

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© The Author(s). 2016

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 8 — Gene structure and functional protein domains of bZIP17 isoforms. bZIP17 SVs were identified as potential products of IRE1A through co-expression and co-splicing network analyses. a bZIP17 gene/pre-mRNA structure (exons are brown and introns are green) and the location of the predicted conserved motif in the R1 intron/exon splice junctions (teal circles) on the pre-mRNA. The predicted cryptic splice site is located in the middle of the second exon. b Protein isoforms encoded by the bZIP17.1 and bZIP17.N2 SVs with the location of a basic-leucine zipper domain. The interruption of the second exon with a short unconventional intron in bZIP17.N2 results in the truncation of this domain.