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      Nephromyces Encodes a Urate Metabolism Pathway and Predicted Peroxisomes, Demonstrating That These Are Not Ancient Losses of Apicomplexans

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          Abstract

          The phylum Apicomplexa is a quintessentially parasitic lineage, whose members infect a broad range of animals. One exception to this may be the apicomplexan genus Nephromyces, which has been described as having a mutualistic relationship with its host. Here we analyze transcriptome data from Nephromyces and its parasitic sister taxon, Cardiosporidium, revealing an ancestral purine degradation pathway thought to have been lost early in apicomplexan evolution. The predicted localization of many of the purine degradation enzymes to peroxisomes, and the in silico identification of a full set of peroxisome proteins, indicates that loss of both features in other apicomplexans occurred multiple times. The degradation of purines is thought to play a key role in the unusual relationship between Nephromyces and its host. Transcriptome data confirm previous biochemical results of a functional pathway for the utilization of uric acid as a primary nitrogen source for this unusual apicomplexan.

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          Most cited references66

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          PSORT: a program for detecting sorting signals in proteins and predicting their subcellular localization.

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            Predotar: A tool for rapidly screening proteomes for N-terminal targeting sequences.

            Probably more than 25% of the proteins encoded by the nuclear genomes of multicellular eukaryotes are targeted to membrane-bound compartments by N-terminal targeting signals. The major signals are those for the endoplasmic reticulum, the mitochondria, and in plants, plastids. The most abundant of these targeted proteins are well-known and well-studied, but a large proportion remain unknown, including most of those involved in regulation of organellar gene expression or regulation of biochemical pathways. The discovery and characterization of these proteins by biochemical means will be long and difficult. An alternative method is to identify candidate organellar proteins via their characteristic N-terminal targeting sequences. We have developed a neural network-based approach (Predotar--Prediction of Organelle Targeting sequences) for identifying genes encoding these proteins amongst eukaryotic genome sequences. The power of this approach for identifying and annotating novel gene families has been illustrated by the discovery of the pentatricopeptide repeat family.
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              Genomic minimalism in the early diverging intestinal parasite Giardia lamblia.

              The genome of the eukaryotic protist Giardia lamblia, an important human intestinal parasite, is compact in structure and content, contains few introns or mitochondrial relics, and has simplified machinery for DNA replication, transcription, RNA processing, and most metabolic pathways. Protein kinases comprise the single largest protein class and reflect Giardia's requirement for a complex signal transduction network for coordinating differentiation. Lateral gene transfer from bacterial and archaeal donors has shaped Giardia's genome, and previously unknown gene families, for example, cysteine-rich structural proteins, have been discovered. Unexpectedly, the genome shows little evidence of heterozygosity, supporting recent speculations that this organism is sexual. This genome sequence will not only be valuable for investigating the evolution of eukaryotes, but will also be applied to the search for new therapeutics for this parasite.
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                Author and article information

                Contributors
                Role: Associate Editor
                Journal
                Genome Biol Evol
                Genome Biol Evol
                gbe
                Genome Biology and Evolution
                Oxford University Press
                1759-6653
                January 2019
                30 November 2018
                30 November 2018
                : 11
                : 1
                : 41-53
                Affiliations
                [1 ]Department of Biological Sciences, University of Rhode Island
                [2 ]Department of Biochemistry and Molecular Biology, Dalhousie University, Halifax, Nova Scotia, Canada
                [3 ]Smithsonian National Museum of Natural History, Washington, District of Columbia
                Author notes

                Data deposition: This project has been deposited at NCBI GenBank under the accession SAMN10291587.

                Corresponding author: E-mail: clane@ 123456uri.edu .
                Article
                evy251
                10.1093/gbe/evy251
                6320678
                30500900
                d70a05d8-1169-42d3-bf3c-22d22f077911
                © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 28 November 2018
                Page count
                Pages: 13
                Funding
                Funded by: National Institute of Health
                Funded by: NSERC 10.13039/501100000038
                Award ID: RGPIN/05754-2015
                Categories
                Research Article

                Genetics
                apicomplexan,tunicates,peroxisomes,purine degradation,nephromyces,cardiosporidium
                Genetics
                apicomplexan, tunicates, peroxisomes, purine degradation, nephromyces, cardiosporidium

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