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. 2016 Aug 17;17:650. doi: 10.1186/s12864-016-2944-3

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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. 12 — Cnidarian Vitellogenin gene tree. ML topology of all known homologs of the Vitellogenin gene superfamily and apolipophorin-like putative Vitellogenin precursor in cnidarian taxa from NCBI Genbank and transcriptome components of A. alata in this study. Assumes the LG + G model of amino acid evolution, as specified as most appropriate by ProtTest v. 3.2. Shimodaira-Hasegawa-like branch support indices are shown at each node. Grey (top) highlights a clade of apolipophorin-like putative Vitellogenin precursor homologs for cubozoan Carukia barnesi and A. alata from this study and hydrozoan Hydra vulgaris, while the non-highlighted clade (bottom) highlights the relationships among known Vitellogenins of cnidarian taxa. Stars designate transcripts most upregulated in the ovaries (comp74784, comp75374 & comp77096); all others are either most highly expressed in the tentacle (comp35113 & 51914) or equally high in the gastric cirri and tentacle samples (comp57678 & comp75135)