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      Macronuclear Genome Sequence of the Ciliate Tetrahymena thermophila, a Model Eukaryote

      research-article
        1 , ¤a , * , 1 , 1 , 1 , 1 , 1 , 1 , 1 , 1 , 1 , 1 , 1 , ¤b ,   1 , ¤b , 1 , 1 , 1 , ¤c , 1 , ¤d , 1 , ¤e , 1 , ¤f , 2 , 2 , 3 , 4 , 4 , 5 , 6 , ¤g , 6 , 7 , 7 , 8 , 9 , 10 , 10 , 10 , 11 , 11 , ¤h , 11 , 12 , 12 , 13 , 14 , 14 , 15 , 15 , ¤j , 15 , ¤j , 16 , 16 , 16 , 17 , ¤k , 17 , ¤l , 17 , 17 , ¤m , 17 , 17
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          Abstract

          The ciliate Tetrahymena thermophila is a model organism for molecular and cellular biology. Like other ciliates, this species has separate germline and soma functions that are embodied by distinct nuclei within a single cell. The germline-like micronucleus (MIC) has its genome held in reserve for sexual reproduction. The soma-like macronucleus (MAC), which possesses a genome processed from that of the MIC, is the center of gene expression and does not directly contribute DNA to sexual progeny. We report here the shotgun sequencing, assembly, and analysis of the MAC genome of T. thermophila, which is approximately 104 Mb in length and composed of approximately 225 chromosomes. Overall, the gene set is robust, with more than 27,000 predicted protein-coding genes, 15,000 of which have strong matches to genes in other organisms. The functional diversity encoded by these genes is substantial and reflects the complexity of processes required for a free-living, predatory, single-celled organism. This is highlighted by the abundance of lineage-specific duplications of genes with predicted roles in sensing and responding to environmental conditions (e.g., kinases), using diverse resources (e.g., proteases and transporters), and generating structural complexity (e.g., kinesins and dyneins). In contrast to the other lineages of alveolates (apicomplexans and dinoflagellates), no compelling evidence could be found for plastid-derived genes in the genome. UGA, the only T. thermophila stop codon, is used in some genes to encode selenocysteine, thus making this organism the first known with the potential to translate all 64 codons in nuclear genes into amino acids. We present genomic evidence supporting the hypothesis that the excision of DNA from the MIC to generate the MAC specifically targets foreign DNA as a form of genome self-defense. The combination of the genome sequence, the functional diversity encoded therein, and the presence of some pathways missing from other model organisms makes T. thermophila an ideal model for functional genomic studies to address biological, biomedical, and biotechnological questions of fundamental importance.

          Abstract

          The macronuclear genome of Tetrahymena thermophila is sequenced and analyzed. Conservation in this single-celled ciliate of some features normally observed in only multicellular organisms sheds light on early eukaryotic evolution.

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          Most cited references173

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          TRANSFAC: transcriptional regulation, from patterns to profiles.

          The TRANSFAC database on eukaryotic transcriptional regulation, comprising data on transcription factors, their target genes and regulatory binding sites, has been extended and further developed, both in number of entries and in the scope and structure of the collected data. Structured fields for expression patterns have been introduced for transcription factors from human and mouse, using the CYTOMER database on anatomical structures and developmental stages. The functionality of Match, a tool for matrix-based search of transcription factor binding sites, has been enhanced. For instance, the program now comes along with a number of tissue-(or state-)specific profiles and new profiles can be created and modified with Match Profiler. The GENE table was extended and gained in importance, containing amongst others links to LocusLink, RefSeq and OMIM now. Further, (direct) links between factor and target gene on one hand and between gene and encoded factor on the other hand were introduced. The TRANSFAC public release is available at http://www.gene-regulation.com. For yeast an additional release including the latest data was made available separately as TRANSFAC Saccharomyces Module (TSM) at http://transfac.gbf.de. For CYTOMER free download versions are available at http://www.biobase.de:8080/index.html.
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            Rfam: an RNA family database.

            Rfam is a collection of multiple sequence alignments and covariance models representing non-coding RNA families. Rfam is available on the web in the UK at http://www.sanger.ac.uk/Software/Rfam/ and in the US at http://rfam.wustl.edu/. These websites allow the user to search a query sequence against a library of covariance models, and view multiple sequence alignments and family annotation. The database can also be downloaded in flatfile form and searched locally using the INFERNAL package (http://infernal.wustl.edu/). The first release of Rfam (1.0) contains 25 families, which annotate over 50 000 non-coding RNA genes in the taxonomic divisions of the EMBL nucleotide database.
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              The origins of genome complexity.

              Complete genomic sequences from diverse phylogenetic lineages reveal notable increases in genome complexity from prokaryotes to multicellular eukaryotes. The changes include gradual increases in gene number, resulting from the retention of duplicate genes, and more abrupt increases in the abundance of spliceosomal introns and mobile genetic elements. We argue that many of these modifications emerged passively in response to the long-term population-size reductions that accompanied increases in organism size. According to this model, much of the restructuring of eukaryotic genomes was initiated by nonadaptive processes, and this in turn provided novel substrates for the secondary evolution of phenotypic complexity by natural selection. The enormous long-term effective population sizes of prokaryotes may impose a substantial barrier to the evolution of complex genomes and morphologies.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                PLoS Biol
                pbio
                PLoS Biology
                Public Library of Science (San Francisco, USA )
                1544-9173
                1545-7885
                September 2006
                29 August 2006
                : 4
                : 9
                : e286
                Affiliations
                [1 ]The Institute for Genomic Research, Rockville, Maryland, United States of America
                [2 ]Department of Biology, York University, Toronto, Ontario, Canada
                [3 ]Centre for Research in Mass Spectrometry, York University, Toronto, Ontario, Canada
                [4 ]Department of Biological Sciences, Marquette University, Milwaukee, Wisconsin, United States of America
                [5 ]Razavi-Newman Center for Bioinformatics, The Salk Institute for Biological Studies, San Diego, California, United States of America
                [6 ]Department of Molecular Genetics and Cell Biology, University of Chicago, Chicago, Illinois, United States of America
                [7 ] Department of Biology, Harvey Mudd College, Claremont, California, United States of America
                [8 ]Department of Biology, University of Texas at San Antonio, San Antonio, Texas, United States of America
                [9 ]Department of Electrical Engineering, University of Texas at San Antonio, San Antonio, Texas, United States of America
                [10 ]Department of Molecular and Cellular Biology, University of California Berkeley, Berkeley, California, United States of America
                [11 ]Department of Computer Science and Engineering, University of Washington, Seattle, Washington, United States of America
                [12 ]Department of Cellular Biology, University of Georgia, Athens, Georgia, United States of America
                [13 ]Department of Biological Sciences, University of Iowa, Iowa City, Iowa, United States of America
                [14 ]Department of Biology, University of Rochester, Rochester, New York, United States of America
                [15 ]Canadian Institute for Advanced Research, Department of Botany, University of British Columbia, Vancouver, British Columbia, Canada
                [16 ]Department of Genetics, Stanford University, Stanford, California, United States of America
                [17 ]Department of Molecular, Cellular, and Developmental Biology, University of California Santa Barbara, Santa Barbara, California, United States of America
                Institute for Information Transmission Problems, Russian Federation
                Author notes
                * To whom correspondence should be addressed. E-mail: jaeisen@ 123456ucdavis.edu
                Article
                06-PLBI-RA-0010R2 e286 plbi-04-09-14
                10.1371/journal.pbio.0040286
                1557398
                16933976
                2e97708f-ede7-42f6-8326-fd18662e4163
                Copyright: © 2006 Eisen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 4 January 2006
                : 23 June 2006
                Page count
                Pages: 23
                Categories
                Research Article
                Genetics/Genomics/Gene Therapy
                Custom metadata
                Eisen JA, Coyne RS, Wu M, Wu D, Thiagarajan M, et al. (2006) Macronuclear genome sequence of the ciliate Tetrahymena thermophila, a model eukaryote. PLoS Biol 4(9): e286. DOI: 10.1371/journal.pbio.0040286

                Life sciences
                Life sciences

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