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      Biology and genome of a newly discovered sibling species of Caenorhabditis elegans

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          Abstract

          A ‘sibling’ species of the model organism Caenorhabditis elegans has long been sought for use in comparative analyses that would enable deep evolutionary interpretations of biological phenomena. Here, we describe the first sibling species of C. elegans, C. inopinata n. sp., isolated from fig syconia in Okinawa, Japan. We investigate the morphology, developmental processes and behaviour of C. inopinata, which differ significantly from those of C. elegans. The 123-Mb C. inopinata genome was sequenced and assembled into six nuclear chromosomes, allowing delineation of Caenorhabditis genome evolution and revealing unique characteristics, such as highly expanded transposable elements that might have contributed to the genome evolution of C. inopinata. In addition, C. inopinata exhibits massive gene losses in chemoreceptor gene families, which could be correlated with its limited habitat area. We have developed genetic and molecular techniques for C. inopinata; thus C. inopinata provides an exciting new platform for comparative evolutionary studies.

          Abstract

          Caenorhabditis nematodes are important model organisms. Here, the authors report the biology and genome of Caenorhabditis inopinata, a first sibling species of C. elegans, and develop genetic and molecular techniques for C. inopinata.

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          LTRharvest, an efficient and flexible software for de novo detection of LTR retrotransposons

          Background Transposable elements are abundant in eukaryotic genomes and it is believed that they have a significant impact on the evolution of gene and chromosome structure. While there are several completed eukaryotic genome projects, there are only few high quality genome wide annotations of transposable elements. Therefore, there is a considerable demand for computational identification of transposable elements. LTR retrotransposons, an important subclass of transposable elements, are well suited for computational identification, as they contain long terminal repeats (LTRs). Results We have developed a software tool LTRharvest for the de novo detection of full length LTR retrotransposons in large sequence sets. LTRharvest efficiently delivers high quality annotations based on known LTR transposon features like length, distance, and sequence motifs. A quality validation of LTRharvest against a gold standard annotation for Saccharomyces cerevisae and Drosophila melanogaster shows a sensitivity of up to 90% and 97% and specificity of 100% and 72%, respectively. This is comparable or slightly better than annotations for previous software tools. The main advantage of LTRharvest over previous tools is (a) its ability to efficiently handle large datasets from finished or unfinished genome projects, (b) its flexibility in incorporating known sequence features into the prediction, and (c) its availability as an open source software. Conclusion LTRharvest is an efficient software tool delivering high quality annotation of LTR retrotransposons. It can, for example, process the largest human chromosome in approx. 8 minutes on a Linux PC with 4 GB of memory. Its flexibility and small space and run-time requirements makes LTRharvest a very competitive candidate for future LTR retrotransposon annotation projects. Moreover, the structured design and implementation and the availability as open source provides an excellent base for incorporating novel concepts to further improve prediction of LTR retrotransposons.
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            Genome sequence of the nematode C. elegans: a platform for investigating biology.

            (1999)
            The 97-megabase genomic sequence of the nematode Caenorhabditis elegans reveals over 19,000 genes. More than 40 percent of the predicted protein products find significant matches in other organisms. There is a variety of repeated sequences, both local and dispersed. The distinctive distribution of some repeats and highly conserved genes provides evidence for a regional organization of the chromosomes.
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              Efficient gene transfer in C.elegans: extrachromosomal maintenance and integration of transforming sequences.

              We describe a dominant behavioral marker, rol-6(su-1006), and an efficient microinjection procedure which facilitate the recovery of Caenorhabditis elegans transformants. We use these tools to study the mechanism of C.elegans DNA transformation. By injecting mixtures of genetically marked DNA molecules, we show that large extrachromosomal arrays assemble directly from the injected molecules and that homologous recombination drives array assembly. Appropriately placed double-strand breaks stimulated homologous recombination during array formation. Our data indicate that the size of the assembled transgenic structures determines whether or not they will be maintained extrachromosomally or lost. We show that low copy number extrachromosomal transformation can be achieved by adjusting the relative concentration of DNA molecules in the injection mixture. Integration of the injected DNA, though relatively rare, was reproducibly achieved when single-stranded oligonucleotide was co-injected with the double-stranded DNA.
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                Author and article information

                Contributors
                asugimoto@m.tohoku.ac.jp
                taisei_kikuchi@med.miyazaki-u.ac.jp
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                10 August 2018
                10 August 2018
                2018
                : 9
                : 3216
                Affiliations
                [1 ]ISNI 0000 0000 9150 188X, GRID grid.417935.d, Forestry and Forest Products Research Institute, ; Tsukuba, 305-8687 Japan
                [2 ]ISNI 0000 0001 2287 1366, GRID grid.28665.3f, Biodiversity Research Center, , Academia Sinica, ; Taipei city, 11529 Taiwan
                [3 ]ISNI 0000 0001 0657 3887, GRID grid.410849.0, Faculty of Medicine, , University of Miyazaki, ; Miyazaki, 889-1692 Japan
                [4 ]ISNI 0000 0001 2248 6943, GRID grid.69566.3a, Laboratory of Developmental Dynamics, Graduate School of Life Sciences, , Tohoku University, ; Sendai, 980-8577 Japan
                [5 ]ISNI 0000 0004 0606 5382, GRID grid.10306.34, Wellcome Trust Sanger Institute, ; Wellcome Genome Campus, Hinxton, CB10 1SA UK
                [6 ]ISNI 0000000107068890, GRID grid.20861.3d, HHMI and Division of Biology and Biological Engineering, , Caltech, ; Pasadena, CA 91125 USA
                [7 ]ISNI 000000041936877X, GRID grid.5386.8, Boyce Thompson Institute, and Department of Chemistry and Chemical Biology, , Cornell University, ; Ithaca, NY 14853 USA
                [8 ]ISNI 0000 0000 9150 188X, GRID grid.417935.d, Present Address: Kansai Research Center, , Forestry and Forest Products Research Institute, ; 68 Nagaikyutaroh, Momoyama, Fushimi, Kyoto, 612-0855 Japan
                [9 ]ISNI 0000 0004 1936 8008, GRID grid.170202.6, Present Address: Department of Biology, Institute of Ecology and Evolution, , University of Oregon, ; Eugene, OR 97403-5289 USA
                Author information
                http://orcid.org/0000-0001-8752-1674
                http://orcid.org/0000-0002-2123-5058
                http://orcid.org/0000-0002-7805-889X
                http://orcid.org/0000-0003-4698-9961
                http://orcid.org/0000-0001-9167-7532
                http://orcid.org/0000-0002-1217-8231
                http://orcid.org/0000-0002-9581-0377
                http://orcid.org/0000-0002-7699-0173
                http://orcid.org/0000-0001-6001-4293
                http://orcid.org/0000-0003-2759-9167
                Article
                5712
                10.1038/s41467-018-05712-5
                6086898
                30097582
                601edfbc-0c47-4e04-bd3d-ecd103383f0e
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 8 December 2017
                : 19 July 2018
                Funding
                Funded by: FundRef https://doi.org/10.13039/100004440, Wellcome Trust;
                Award ID: 206194
                Award ID: 206194
                Award ID: 206194
                Award Recipient :
                Funded by: Howard Hughes Medical Institute
                Funded by: FundRef https://doi.org/10.13039/501100001691, Japan Society for the Promotion of Science (JSPS);
                Award ID: 26292178
                Award ID: 16H04722
                Award ID: 15K14503
                Award Recipient :
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