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      Population‐specific transcriptional differences associated with freeze tolerance in a terrestrial worm

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          Abstract

          Enchytraeus albidus is a terrestrial earthworm widespread along the coasts of northern Europe and the Arctic. This species tolerates freezing of body fluids and survives winters in a frozen state. Their acclimatory physiological mechanisms behind freeze tolerance involve increased fluidity of membrane lipids during cold exposure and accumulation of cryoprotectants (glucose) during the freezing process. Gene regulatory processes of these physiological responses have not been studied, partly because no gene expression tools were developed. The main aim of this study was to understand whether the freeze tolerance mechanisms have a transcriptomic basis in E. albidus. For that purpose, first the transcriptome of E. albidus was assembled with RNAseq data. Second, two strains from contrasting thermal environments (Germany and Greenland) were compared by mapping barcoded RNAseq data onto the assembled transcriptome. Both of these strains are freeze tolerant, but Greenland is extremely freeze tolerant. Results showed more plastic responses in the Greenland strain as well as higher constitutive expression of particular stress response genes. These altered transcriptional networks are associated with an adapted homeostasis coping with prolonged freezing conditions in Greenland animals. Previously identified physiological alterations in freeze‐tolerant strains of E. albidus are underpinned at the transcriptome level. These processes involve anion transport in the hemolymph, fatty acid metabolism, metabolism, and transport of cryoprotective sugars as well as protection against oxidative stress. Pathway analysis supported most of these processes, and identified additional differentially expressed pathways such as peroxisome and Toll‐like receptor signaling. We propose that the freeze‐tolerant phenotype is the consequence of genetic adaptation to cold stress and may have driven evolutionary divergence of the two strains.

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            Streaming fragment assignment for real-time analysis of sequencing experiments

            We present eXpress, a software package for highly efficient probabilistic assignment of ambiguously mapping sequenced fragments. eXpress uses a streaming algorithm with linear run time and constant memory use. It can determine abundances of sequenced molecules in real time, and can be applied to ChIP-seq, metagenomics and other large-scale sequencing data. We demonstrate its use on RNA-seq data, showing greater efficiency than other quantification methods.
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              Reverse transcriptase template switching: a SMART approach for full-length cDNA library construction.

              Here, we describe a fast, simple method for constructing full-length cDNA libraries using SMART technology. This novel procedure uses the template-switching activity of Moloney murine leukemia virus (MMLV) reverse transcriptase to synthesize and anchor first-strand cDNA in one step. Following reverse transcription, three cycles of PCR are performed using a modified oligo(dT) primer and an anchor primer to enrich the cDNA population for full-length sequences. Starting with 1 microgram human skeletal muscle poly(A)+ RNA, a cDNA library was constructed that contained 3 x 10(6) independent clones with an average insert size of 2 kb. Sequence analysis of 172 randomly selected clones showed that 77% of cDNA clones corresponding to known genes contained intact open reading frames. The average length of complete open reading frames was 2.4 kb. Furthermore, 86% of the full-length clones retained longer 5' UTR sequences than the longest 5' end deposited in the GenBank database. cDNA libraries generated using this method will be useful for accelerating the collection of mRNA 5' end sequence information, which is currently very limited in GenBank.
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                Author and article information

                Contributors
                dick.roelofs@vu.nl
                Journal
                Ecol Evol
                Ecol Evol
                10.1002/(ISSN)2045-7758
                ECE3
                Ecology and Evolution
                John Wiley and Sons Inc. (Hoboken )
                2045-7758
                11 March 2018
                April 2018
                : 8
                : 7 ( doiID: 10.1002/ece3.2018.8.issue-7 )
                : 3774-3786
                Affiliations
                [ 1 ] Microlife Solutions Amsterdam The Netherlands
                [ 2 ] Department of Ecological Science Faculty of Earth and Life Sciences VU University, Amsterdam Amsterdam The Netherlands
                [ 3 ] Department of Bioscience Aarhus University Silkeborg Denmark
                [ 4 ] Department of Biology and CESAM (Centre for Environmental and Marine Studies) University of Aveiro Aveiro Portugal
                Author notes
                [*] [* ] Correspondence

                Dick Roelofs, Department of Ecological Science, Faculty of Earth and Life Sciences, VU University, Amsterdam, Amsterdam, The Netherlands.

                Email: dick.roelofs@ 123456vu.nl

                Author information
                http://orcid.org/0000-0003-3954-3590
                Article
                ECE33602
                10.1002/ece3.3602
                5901168
                5aa137b7-b9b0-4375-8ef6-7144eb808d37
                © 2017 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 23 June 2017
                : 13 October 2017
                : 13 October 2017
                Page count
                Figures: 6, Tables: 2, Pages: 13, Words: 9392
                Funding
                Funded by: BE‐BASIC foundation
                Award ID: F08.001.03
                Award ID: F07.003.05
                Funded by: EU FP7 program Sustainable Nanotechnologies (SUN)
                Award ID: 604305
                Funded by: NM_OREO
                Award ID: POCI‐01‐0145‐FEDER‐016771
                Award ID: PTDC/AAG‐MAA/4084/2014
                Funded by: CESAM
                Award ID: UID/AMB/50017
                Funded by: FEDER through COMPETE Programa Operacional Factores de Competitividade, through FCT‐Fundação para a Ciência e Tecnologia
                Funded by: PT2020 Partnership Agreement and Compete 2020
                Funded by: The Danish Council for Independent Research
                Award ID: 10‐084579
                Categories
                Original Research
                Original Research
                Custom metadata
                2.0
                ece33602
                April 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.3.4 mode:remove_FC converted:16.04.2018

                Evolutionary Biology
                cryoprotectant,membrane lipid,oxidative stress,rnaseq,sodium transport,transcriptional plasticity

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