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      Exploring the genomic diversity of black yeasts and relatives ( Chaetothyriales, Ascomycota)

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          Abstract

          The order Chaetothyriales ( Pezizomycotina, Ascomycetes) harbours obligatorily melanised fungi and includes numerous etiologic agents of chromoblastomycosis, phaeohyphomycosis and other diseases of vertebrate hosts. Diseases range from mild cutaneous to fatal cerebral or disseminated infections and affect humans and cold-blooded animals globally. In addition, Chaetothyriales comprise species with aquatic, rock-inhabiting, ant-associated, and mycoparasitic life-styles, as well as species that tolerate toxic compounds, suggesting a high degree of versatile extremotolerance. To understand their biology and divergent niche occupation, we sequenced and annotated a set of 23 genomes of main the human opportunists within the Chaetothyriales as well as related environmental species. Our analyses included fungi with diverse life-styles, namely opportunistic pathogens and closely related saprobes, to identify genomic adaptations related to pathogenesis. Furthermore, ecological preferences of Chaetothyriales were analysed, in conjuncture with the order-level phylogeny based on conserved ribosomal genes. General characteristics, phylogenomic relationships, transposable elements, sex-related genes, protein family evolution, genes related to protein degradation (MEROPS), carbohydrate-active enzymes (CAZymes), melanin synthesis and secondary metabolism were investigated and compared between species. Genome assemblies varied from 25.81 Mb ( Capronia coronata) to 43.03 Mb ( Cladophialophora immunda). The bantiana-clade contained the highest number of predicted genes (12 817 on average) as well as larger genomes. We found a low content of mobile elements, with DNA transposons from Tc1/Mariner superfamily being the most abundant across analysed species. Additionally, we identified a reduction of carbohydrate degrading enzymes, specifically many of the Glycosyl Hydrolase (GH) class, while most of the Pectin Lyase (PL) genes were lost in etiological agents of chromoblastomycosis and phaeohyphomycosis. An expansion was found in protein degrading peptidase enzyme families S12 (serine-type D-Ala-D-Ala carboxypeptidases) and M38 (isoaspartyl dipeptidases). Based on genomic information, a wide range of abilities of melanin biosynthesis was revealed; genes related to metabolically distinct DHN, DOPA and pyomelanin pathways were identified. The MAT ( MAting Type) locus and other sex-related genes were recognized in all 23 black fungi. Members of the asexual genera Fonsecaea and Cladophialophora appear to be heterothallic with a single copy of either MAT-1-1 or MAT-1-2 in each individual. All Capronia species are homothallic as both MAT1-1 and MAT1-2 genes were found in each single genome. The genomic synteny of the MAT-locus flanking genes (SLA2-APN2-COX13) is not conserved in black fungi as is commonly observed in Eurotiomycetes, indicating a unique genomic context for MAT in those species. The heterokaryon (het) genes expansion associated with the low selective pressure at the MAT-locus suggests that a parasexual cycle may play an important role in generating diversity among those fungi.

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          Much of natural product chemistry concerns a group of compounds known as secondary metabolites. These low-molecular-weight metabolites often have potent physiological activities. Digitalis, morphine and quinine are plant secondary metabolites, whereas penicillin, cephalosporin, ergotrate and the statins are equally well known fungal secondary metabolites. Although chemically diverse, all secondary metabolites are produced by a few common biosynthetic pathways, often in conjunction with morphological development. Recent advances in molecular biology, bioinformatics and comparative genomics have revealed that the genes encoding specific fungal secondary metabolites are clustered and often located near telomeres. In this review, we address some important questions, including which evolutionary pressures led to gene clustering, why closely related species produce different profiles of secondary metabolites, and whether fungal genomics will accelerate the discovery of new pharmacologically active natural products.
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            The fungal cell wall is a dynamic structure that protects the cell from changes in osmotic pressure and other environmental stresses, while allowing the fungal cell to interact with its environment. The structure and biosynthesis of a fungal cell wall is unique to the fungi, and is therefore an excellent target for the development of anti-fungal drugs. The structure of the fungal cell wall and the drugs that target its biosynthesis are reviewed. Based on studies in a number of fungi, the cell wall has been shown to be primarily composed of chitin, glucans, mannans and glycoproteins. The biosynthesis of the various components of the fungal cell wall and the importance of the components in the formation of a functional cell wall, as revealed through mutational analyses, are discussed. There is strong evidence that the chitin, glucans and glycoproteins are covalently cross-linked together and that the cross-linking is a dynamic process that occurs extracellularly. (c) 2006 Wiley Periodicals, Inc.
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              TCDB: the Transporter Classification Database for membrane transport protein analyses and information

              The Transporter Classification Database (TCDB) is a web accessible, curated, relational database containing sequence, classification, structural, functional and evolutionary information about transport systems from a variety of living organisms. TCDB is a curated repository for factual information compiled from >10 000 references, encompassing ∼3000 representative transporters and putative transporters, classified into >400 families. The transporter classification (TC) system is an International Union of Biochemistry and Molecular Biology approved system of nomenclature for transport protein classification. TCDB is freely accessible at . The web interface provides several different methods for accessing the data, including step-by-step access to hierarchical classification, direct search by sequence or TC number and full-text searching. The functional ontology that underlies the database structure facilitates powerful query searches that yield valuable data in a quick and easy way. The TCDB website also offers several tools specifically designed for analyzing the unique characteristics of transport proteins. TCDB not only provides curated information and a tool for classifying newly identified membrane proteins, but also serves as a genome transporter-annotation tool.
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                Author and article information

                Contributors
                Journal
                Stud Mycol
                Stud. Mycol
                Studies in Mycology
                CBS Fungal Biodiversity Centre
                0166-0616
                1872-9797
                27 January 2017
                March 2017
                27 January 2017
                : 86
                : 1-28
                Affiliations
                [1 ]Division of Pathogen Genomics, Translational Genomics Research Institute (TGen), Flagstaff, AZ, USA
                [2 ]Department of Cell Biology, University of Brasília, Brasilia, Brazil
                [3 ]Westerdijk Fungal Biodiversity Institute, Utrecht, The Netherlands
                [4 ]Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland
                [5 ]Université Aix-Marseille (CNRS), Marseille, France
                [6 ]The National Laboratory for Scientific Computing (LNCC), Petropolis, Brazil
                [7 ]Broad Institute of MIT and Harvard, Cambridge, USA
                [8 ]Department of Biochemistry, University of São Paulo, Brazil
                [9 ]Department of Biological Sciences, Federal University of São Paulo, Diadema, SP, Brazil
                [10 ]Núcleo Multidisciplinar de Pesquisa em Biologia UFRJ-Xerém-NUMPEX-BIO, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil
                [11 ]Department of Basic Pathology, Federal University of Paraná State, Curitiba, PR, Brazi1
                [12 ]Department of Biochemistry and Molecular Biology, Federal University of Paraná, Curitiba, PR, Brazil
                [13 ]Department of Clinical and Toxicological Analysis, University of São Paulo, São Paulo, SP, Brazil
                [14 ]Institute of Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam, The Netherlands
                [15 ]Shanghai Institute of Medical Mycology, Changzheng Hospital, Second Military Medical University, Shanghai, China
                [16 ]Department of Systematic and Evolutionary Botany, University of Vienna, Vienna, Austria
                [17 ]Biological Sciences Department, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia
                [18 ]Botany and Microbiology Department, Faculty of Science, Cairo University, Giza, Egypt
                [19 ]Federal Institute for Material Research and Testing (BAM), Berlin, Germany
                Author notes
                [] Correspondence: C.A. Cuomo; G. Sybren de Hoog cuomo@ 123456broadinstitute.org s.hoog@ 123456westerdijkinstitute.nl
                [21]

                These authors contributed equally to the manuscript.

                Article
                S0166-0616(17)30016-7
                10.1016/j.simyco.2017.01.001
                5358931
                28348446
                9ed21b8a-81e5-4c20-b3da-50820e18a0bc
                © 2017 Westerdijk Fungal Biodiversity Institute. Production and hosting by ELSEVIER B.V.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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                Categories
                Research Paper

                Plant science & Botany
                black yeast,comparative genomics,chaetothyriales,ecology,evolution,herpotrichiellaceae,phylogeny

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