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. 2017 Jan 2;45(8):4722–4732. doi: 10.1093/nar/gkw1318

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© The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 1. — Spt5 proteins in Paramecium. (A) Predicted protein domains (colored boxes) for Paramecium tetraurelia, Tetrahymena thermophila, Homo sapiens, Saccharomyces cerevisiae and Arabidopsis thaliana Spt5 proteins. (B) Neighbor-joining tree of Spt5 proteins from ciliates based on the alignment of entire protein sequences (461 positions in the final dataset) and the following parameters: bootstrap 1000 (bootstrap values displayed next to the branches) and Poisson correction. Ptet, P. tetraurelia; Pbi, Paramecium biaurelia; Psex, Paramecium sexaurelia; Pcaud, Paramecium caudatum; Ot, Oxytricha trifallax; Tt, T. thermophila, human (Hs) and arabidopsis (At). (C) Autogamy time-course of gene expression for P. tetraurelia SPT5 (GSPATG00013468001, GSPATG00023145001), DCL2 (GSPATG00008494001), DCL3 (GSPATG00027456001) and SPO11 (GSPATG00009108001). The Y-axis shows the log2 signals from custom microarrays (55,59).

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