TY - JOUR A1 - Schmidt, Hanno A1 - Tzovaras, Bastian Greshake A1 - Feldmeyer, Barbara A1 - Hankeln, Thomas A1 - Pfenninger, Markus T1 - Genomic basis of ecological niche divergence among cryptic sister species of non-biting midges T2 - BMC genomics N2 - Background: There is a lack of understanding the evolutionary forces driving niche segregation of closely related organisms. In addition, pinpointing the genes driving ecological divergence is a key goal in molecular ecology. Here, larval transcriptome sequences obtained by next-generation-sequencing are used to address these issues in a morphologically cryptic sister species pair of non-biting midges (Chironomus riparius and C. piger). Results: More than eight thousand orthologous open reading frames were screened for interspecific divergence and intraspecific polymorphisms. Despite a small mean sequence divergence of 1.53% between the sister species, 25.1% of 18,115 observed amino acid substitutions were inferred by α statistics to be driven by positive selection. Applying McDonald-Kreitman tests to 715 alignments of gene orthologues identified eleven (1.5%) genes driven by positive selection. Conclusions: Three candidate genes were identified as potentially responsible for the observed niche segregation concerning nitrite concentration, habitat temperature and water conductivity. Additionally, signs of positive selection in the hydrogen sulfide detoxification pathway were detected, providing a new plausible hypothesis for the species’ ecological differentiation. Finally, a divergently selected, nuclear encoded mitochondrial ribosomal protein may contribute to reproductive isolation due to cytonuclear coevolution. KW - Adaptive sequence evolution KW - Positive selection KW - McDonald-Kreitman test KW - Chironomus riparius KW - Chironomus piger Y1 - 2013 UR - http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/31513 UR - https://nbn-resolving.org/urn:nbn:de:hebis:30:3-315130 SN - 1471-2164 N1 - © 2013 Schmidt et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. VL - 14 IS - Art. 384 SP - 1 EP - 11 PB - BioMed Central ; Springer CY - London ; Berlin ; Heidelberg ER -