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. 2013 Oct 25;5(11):2124–2140. doi: 10.1093/gbe/evt161

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© The Author(s) 2013. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 5.— — Phylogenetic trees of the RNase1 (A), RNase4 (B), and RNase5 (C) genes of the littler brown bat (Ml) and the flying fox (Pv, Pteropus vampyrus). The human (Hs) genes were used to root the tree. The isoelectric points of the human and little brown bat proteins are shown next to the functional genes in three tree. (D) Scaffold maps of the little brown bat RNase genes drawn to scale. We followed the same labeling system as figure 1. Pairwise synonymous (d_S) and nonsynonymous (d_N) nucleotide distances between paralogous RNase1 (E), RNase4 (F), and RNase5 (G) genes in the little brown bat. The scale bar number indicates the number of nucleotide substitutions per site.