-K. Rhee from the KBSI Western Seoul Center (T34525), and to D. Kim from Jeju Center (C34290) of Korea Basic Science Institute. “
“Chilean freshwater systems have a reduced number (44) of native fish species; 64% of them have been considered to fall within the vulnerable or threatened category (Vila et al., 2006). The main factors responsible for this situation are habitat fragmentation, invasive species and pollution, all of them produced by human activities. Knowledge of the biology and ecology of these fishes is limited (Habit et al., 2006 and Vila et al., 2006), thus studies analyzing the effects of anthropic activity on native species are fundamental to take appropriate conservation measures for each

species. Basilichthys microlepidotus is an atherinopsid endemic to Chile that inhabits lakes and rivers from 28°S to 39°S ( Quezada-Romegialli et al., 2010 and Veliz Palbociclib nmr et al., 2012). It is a microphagous species, feeding on insect larvae, small invertebrates, filamentous algae and detritus ( Duarte et al., 1971). It has been pointed out that it can survive in highly polluted rivers ( Vega-Retter et al., 2014). Considering that B. microlepidotus is indicated as an endangered species ( Vila et al., 2006), future conservation measures will need information about its health, stress responses and adaptive responses to

human activity. Transcriptomics studies using Next-Generation Sequencing generate a large amount of data that contribute to the understanding of how species interact with their environment and their response selleck products to the current Acetophenone environmental change (Vera et al., 2008). The aim of this study was to characterize the liver transcriptome of B. microlepidotus in order to facilitate future studies on gene expression and the effects of the human

activity, and the development of appropriate conservation strategies for this species. Three individuals of B. microlepidotus were collected in the Maipo River basin; the liver tissues were transported in RNA-later (Life Technologies) to the laboratory. RNA extraction and purification were performed with the PureLink™ RNA Mini Kit (Ambion) and the MicroPoly(A) Purist™ kit (Ambion), respectively. Total RNA was checked using an Agilent Model 2100 Bioanalyzer at OMICS Solutions (Santiago, Chile). Three separate barcoded libraries were constructed with the Ion Total RNA-Seq Kit v2 (Life Technologies) and sequenced in an Ion Torrent platform using the Ion 318 chip in OMICS Solutions (Santiago, Chile). Short read and quality filtration were performed with PRINSEQ ( Schmieder and Edwards, 2011) and TRIMMOMATIC ( Bolger et al., 2014) software. More details are given in the Supplementary methods. A total of 7.8 million reads were obtained from the sequencing performed. After the trimming process 5.93 million reads were retained for the de novo assembly performed with the MIRA assembler (Cheveruex et al., 1999).