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Dive into the research topics where Barbara Robbertse is active.

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Featured researches published by Barbara Robbertse.


Nature Biotechnology | 2008

Genome sequencing and analysis of the biomass-degrading fungus Trichoderma reesei (syn. Hypocrea jecorina).

Diego Martinez; Randy M. Berka; Bernard Henrissat; Markku Saloheimo; Mikko Arvas; Scott E. Baker; Jarod Chapman; Olga Chertkov; Pedro M. Coutinho; Dan Cullen; Etienne Danchin; Igor V. Grigoriev; Paul Harris; Melissa Jackson; Christian P. Kubicek; Cliff Han; Isaac Ho; Luis F. Larrondo; Alfredo Lopez de Leon; Jon K. Magnuson; Sandy Merino; Monica Misra; Beth Nelson; Nicholas H. Putnam; Barbara Robbertse; Asaf Salamov; Monika Schmoll; Astrid Terry; Nina Thayer; Ann Westerholm-Parvinen

Trichoderma reesei is the main industrial source of cellulases and hemicellulases used to depolymerize biomass to simple sugars that are converted to chemical intermediates and biofuels, such as ethanol. We assembled 89 scaffolds (sets of ordered and oriented contigs) to generate 34 Mbp of nearly contiguous T. reesei genome sequence comprising 9,129 predicted gene models. Unexpectedly, considering the industrial utility and effectiveness of the carbohydrate-active enzymes of T. reesei, its genome encodes fewer cellulases and hemicellulases than any other sequenced fungus able to hydrolyze plant cell wall polysaccharides. Many T. reesei genes encoding carbohydrate-active enzymes are distributed nonrandomly in clusters that lie between regions of synteny with other Sordariomycetes. Numerous genes encoding biosynthetic pathways for secondary metabolites may promote survival of T. reesei in its competitive soil habitat, but genome analysis provided little mechanistic insight into its extraordinary capacity for protein secretion. Our analysis, coupled with the genome sequence data, provides a roadmap for constructing enhanced T. reesei strains for industrial applications such as biofuel production.


Nucleic Acids Research | 2016

Reference sequence (RefSeq) database at NCBI: current status, taxonomic expansion, and functional annotation

Nuala A. O'Leary; Mathew W. Wright; J. Rodney Brister; Stacy Ciufo; Diana Haddad; Richard McVeigh; Bhanu Rajput; Barbara Robbertse; Brian Smith-White; Danso Ako-adjei; Alexander Astashyn; Azat Badretdin; Yiming Bao; Olga Blinkova; Vyacheslav Brover; Vyacheslav Chetvernin; Jinna Choi; Eric Cox; Olga Ermolaeva; Catherine M. Farrell; Tamara Goldfarb; Tripti Gupta; Daniel H. Haft; Eneida Hatcher; Wratko Hlavina; Vinita Joardar; Vamsi K. Kodali; Wenjun Li; Donna Maglott; Patrick Masterson

The RefSeq project at the National Center for Biotechnology Information (NCBI) maintains and curates a publicly available database of annotated genomic, transcript, and protein sequence records (http://www.ncbi.nlm.nih.gov/refseq/). The RefSeq project leverages the data submitted to the International Nucleotide Sequence Database Collaboration (INSDC) against a combination of computation, manual curation, and collaboration to produce a standard set of stable, non-redundant reference sequences. The RefSeq project augments these reference sequences with current knowledge including publications, functional features and informative nomenclature. The database currently represents sequences from more than 55 000 organisms (>4800 viruses, >40 000 prokaryotes and >10 000 eukaryotes; RefSeq release 71), ranging from a single record to complete genomes. This paper summarizes the current status of the viral, prokaryotic, and eukaryotic branches of the RefSeq project, reports on improvements to data access and details efforts to further expand the taxonomic representation of the collection. We also highlight diverse functional curation initiatives that support multiple uses of RefSeq data including taxonomic validation, genome annotation, comparative genomics, and clinical testing. We summarize our approach to utilizing available RNA-Seq and other data types in our manual curation process for vertebrate, plant, and other species, and describe a new direction for prokaryotic genomes and protein name management.


Systematic Biology | 2009

The ascomycota tree of life: A phylum-wide phylogeny clarifies the origin and evolution of fundamental reproductive and ecological traits

Conrad L. Schoch; Gi Ho Sung; Francesc López-Giráldez; Jeffrey P. Townsend; Jolanta Miadlikowska; Valérie Hofstetter; Barbara Robbertse; P. Brandon Matheny; Frank Kauff; Zheng Wang; Cécile Gueidan; Rachael M. Andrie; Kristin M. Trippe; Linda M. Ciufetti; Anja Amtoft Wynns; Emily Fraker; Brendan P. Hodkinson; Gregory Bonito; Johannes Z. Groenewald; Mahdi Arzanlou; G. Sybren de Hoog; Pedro W. Crous; David Hewitt; Donald H. Pfister; Kristin R. Peterson; Marieka Gryzenhout; Michael J. Wingfield; André Aptroot; Sung Oui Suh; Meredith Blackwell

We present a 6-gene, 420-species maximum-likelihood phylogeny of Ascomycota, the largest phylum of Fungi. This analysis is the most taxonomically complete to date with species sampled from all 15 currently circumscribed classes. A number of superclass-level nodes that have previously evaded resolution and were unnamed in classifications of the Fungi are resolved for the first time. Based on the 6-gene phylogeny we conducted a phylogenetic informativeness analysis of all 6 genes and a series of ancestral character state reconstructions that focused on morphology of sporocarps, ascus dehiscence, and evolution of nutritional modes and ecologies. A gene-by-gene assessment of phylogenetic informativeness yielded higher levels of informativeness for protein genes (RPB1, RPB2, and TEF1) as compared with the ribosomal genes, which have been the standard bearer in fungal systematics. Our reconstruction of sporocarp characters is consistent with 2 origins for multicellular sexual reproductive structures in Ascomycota, once in the common ancestor of Pezizomycotina and once in the common ancestor of Neolectomycetes. This first report of dual origins of ascomycete sporocarps highlights the complicated nature of assessing homology of morphological traits across Fungi. Furthermore, ancestral reconstruction supports an open sporocarp with an exposed hymenium (apothecium) as the primitive morphology for Pezizomycotina with multiple derivations of the partially (perithecia) or completely enclosed (cleistothecia) sporocarps. Ascus dehiscence is most informative at the class level within Pezizomycotina with most superclass nodes reconstructed equivocally. Character-state reconstructions support a terrestrial, saprobic ecology as ancestral. In contrast to previous studies, these analyses support multiple origins of lichenization events with the loss of lichenization as less frequent and limited to terminal, closely related species.


Science | 2011

Comparative Functional Genomics of the Fission Yeasts

Nicholas Rhind; Zehua Chen; Moran Yassour; Dawn Anne Thompson; Brian J. Haas; Naomi Habib; Ilan Wapinski; Sushmita Roy; Michael F. Lin; David I. Heiman; Sarah K. Young; Kanji Furuya; Yabin Guo; Alison L. Pidoux; Huei Mei Chen; Barbara Robbertse; Jonathan M. Goldberg; Keita Aoki; Elizabeth H. Bayne; Aaron M. Berlin; Christopher A. Desjardins; Edward Dobbs; Livio Dukaj; Lin Fan; Michael Fitzgerald; Courtney French; Sharvari Gujja; Klavs Wörgler Hansen; Daniel Keifenheim; Joshua Z. Levin

A combined analysis of genome sequence, structure, and expression gives insights into fission yeast biology. The fission yeast clade—comprising Schizosaccharomyces pombe, S. octosporus, S. cryophilus, and S. japonicus—occupies the basal branch of Ascomycete fungi and is an important model of eukaryote biology. A comparative annotation of these genomes identified a near extinction of transposons and the associated innovation of transposon-free centromeres. Expression analysis established that meiotic genes are subject to antisense transcription during vegetative growth, which suggests a mechanism for their tight regulation. In addition, trans-acting regulators control new genes within the context of expanded functional modules for meiosis and stress response. Differences in gene content and regulation also explain why, unlike the budding yeast of Saccharomycotina, fission yeasts cannot use ethanol as a primary carbon source. These analyses elucidate the genome structure and gene regulation of fission yeast and provide tools for investigation across the Schizosaccharomyces clade.


Studies in Mycology | 2009

A class-wide phylogenetic assessment of Dothideomycetes

Conrad L. Schoch; Pedro W. Crous; Johannes Z. Groenewald; Eric W.A. Boehm; T. Burgess; J. de Gruyter; G.S. de Hoog; L. J. Dixon; Martin Grube; Cécile Gueidan; Yukio Harada; Satoshi Hatakeyama; Kazuyuki Hirayama; Tsuyoshi Hosoya; Sabine M. Huhndorf; Kevin D. Hyde; E.B.G. Jones; Jan Kohlmeyer; Åsa Kruys; Yan Li; R. Lücking; H.T. Lumbsch; Ludmila Marvanová; J.S. Mbatchou; A. H.. McVay; Andrew N. Miller; G.K. Mugambi; Lucia Muggia; Matthew P. Nelsen; P. Nelson

We present a comprehensive phylogeny derived from 5 genes, nucSSU, nucLSU rDNA, TEF1, RPB1 and RPB2, for 356 isolates and 41 families (six newly described in this volume) in Dothideomycetes. All currently accepted orders in the class are represented for the first time in addition to numerous previously unplaced lineages. Subclass Pleosporomycetidae is expanded to include the aquatic order Jahnulales. An ancestral reconstruction of basic nutritional modes supports numerous transitions from saprobic life histories to plant associated and lichenised modes and a transition from terrestrial to aquatic habitats are confirmed. Finally, a genomic comparison of 6 dothideomycete genomes with other fungi finds a high level of unique protein associated with the class, supporting its delineation as a separate taxon.


Scientific Reports | 2011

Phylogenomic evidence for a common ancestor of mitochondria and the SAR11 clade

J. Cameron Thrash; Alex Boyd; Megan J. Huggett; Jana Grote; Paul Carini; Ryan J. Yoder; Barbara Robbertse; Joseph W. Spatafora; Michael S. Rappé; Stephen J. Giovannoni

Mitochondria share a common ancestor with the Alphaproteobacteria, but determining their precise origins is challenging due to inherent difficulties in phylogenetically reconstructing ancient evolutionary events. Nonetheless, phylogenetic accuracy improves with more refined tools and expanded taxon sampling. We investigated mitochondrial origins with the benefit of new, deeply branching genome sequences from the ancient and prolific SAR11 clade of Alphaproteobacteria and publicly available alphaproteobacterial and mitochondrial genome sequences. Using the automated phylogenomic pipeline Hal, we systematically studied the effect of taxon sampling and missing data to accommodate small mitochondrial genomes. The evidence supports a common origin of mitochondria and SAR11 as a sister group to the Rickettsiales. The simplest explanation of these data is that mitochondria evolved from a planktonic marine alphaproteobacterial lineage that participated in multiple inter-specific cell colonization events, in some cases yielding parasitic relationships, but in at least one case producing a symbiosis that characterizes modern eukaryotic life.


BMC Genomics | 2014

Transposable element-assisted evolution and adaptation to host plant within the Leptosphaeria maculans-Leptosphaeria biglobosa species complex of fungal pathogens

Jonathan Grandaubert; Rohan Gt Lowe; Jessica Louise Soyer; Conrad L. Schoch; Angela P. Van de Wouw; Isabelle Fudal; Barbara Robbertse; Nicolas Lapalu; Matthew G. Links; Benedicte Ollivier; Juliette Linglin; Valérie Barbe; Sophie Mangenot; Corinne Cruaud; Hossein Borhan; Barbara J. Howlett; Marie-Hélène Balesdent; Thierry Rouxel

BackgroundMany plant-pathogenic fungi have a tendency towards genome size expansion, mostly driven by increasing content of transposable elements (TEs). Through comparative and evolutionary genomics, five members of the Leptosphaeria maculans-Leptosphaeria biglobosa species complex (class Dothideomycetes, order Pleosporales), having different host ranges and pathogenic abilities towards cruciferous plants, were studied to infer the role of TEs on genome shaping, speciation, and on the rise of better adapted pathogens.ResultsL. maculans ‘brassicae’, the most damaging species on oilseed rape, is the only member of the species complex to have a TE-invaded genome (32.5%) compared to the other members genomes (<4%). These TEs had an impact at the structural level by creating large TE-rich regions and are suspected to have been instrumental in chromosomal rearrangements possibly leading to speciation. TEs, associated with species-specific genes involved in disease process, also possibly had an incidence on evolution of pathogenicity by promoting translocations of effector genes to highly dynamic regions and thus tuning the regulation of effector gene expression in planta.ConclusionsInvasion of L. maculans ‘brassicae’ genome by TEs followed by bursts of TE activity allowed this species to evolve and to better adapt to its host, making this genome species a peculiarity within its own species complex as well as in the Pleosporales lineage.


PLOS Currents | 2011

Hal: an Automated Pipeline for Phylogenetic Analyses of Genomic Data

Barbara Robbertse; Ryan J. Yoder; Alexander E. Boyd; John Reeves; Joseph W. Spatafora

The rapid increase in genomic and genome-scale data is resulting in unprecedented levels of discrete sequence data available for phylogenetic analyses. Major analytical impasses exist, however, prior to analyzing these data with existing phylogenetic software. Obstacles include the management of large data sets without standardized naming conventions, identification and filtering of orthologous clusters of proteins or genes, and the assembly of alignments of orthologous sequence data into individual and concatenated super alignments. Here we report the production of an automated pipeline, Hal that produces multiple alignments and trees from genomic data. These alignments can be produced by a choice of four alignment programs and analyzed by a variety of phylogenetic programs. In short, the Hal pipeline connects the programs BLASTP, MCL, user specified alignment programs, GBlocks, ProtTest and user specified phylogenetic programs to produce species trees. The script is available at sourceforge (http://sourceforge.net/projects/bio-hal/). The results from an example analysis of Kingdom Fungi are briefly discussed.


IMA Fungus | 2013

MycoBank gearing up for new horizons.

V. Robert; D. Vu; Ammar Ben Hadj Amor; Nathalie van de Wiele; Carlo P.J.M. Brouwer; B. Jabas; Szaniszlo Szoke; Ahmed Dridi; Maher Triki; Samy ben Daoud; Oussema Chouchen; Lea Vaas; Arthur de Cock; Joost A. Stalpers; Dora Stalpers; G.J.M. Verkley; Marizeth Groenewald; Felipe Borges dos Santos; Gerrit Stegehuis; Wei Li; Linhuan Wu; Run Zhang; Juncai Ma; Miaomiao Zhou; Sergio Pérez Gorjón; Lily Eurwilaichitr; Supawadee Ingsriswang; Karen Hansen; Conrad L. Schoch; Barbara Robbertse

MycoBank, a registration system for fungi established in 2004 to capture all taxonomic novelties, acts as a coordination hub between repositories such as Index Fungorum and Fungal Names. Since January 2013, registration of fungal names is a mandatory requirement for valid publication under the International Code of Nomenclature for algae, fungi and plants (ICN). This review explains the database innovations that have been implemented over the past few years, and discusses new features such as advanced queries, registration of typification events (MBT numbers for lecto, epi- and neotypes), the multi-lingual database interface, the nomenclature discussion forum, annotation system, and web services with links to third parties. MycoBank has also introduced novel identification services, linking DNA sequence data to numerous related databases to enable intelligent search queries. Although MycoBank fills an important void for taxon registration, challenges for the future remain to improve links between taxonomic names and DNA data, and to also introduce a formal system for naming fungi known from DNA sequence data only. To further improve the quality of MycoBank data, remote access will now allow registered mycologists to act as MycoBank curators, using Citrix software.


IMA Fungus | 2014

The Genera of Fungi: fixing the application of type species of generic names.

Pedro W. Crous; Alejandra Giraldo; David L. Hawksworth; V. Robert; Paul M. Kirk; Josep Guarro; Barbara Robbertse; Conrad L. Schoch; Ulrike Damm; Thippawan Trakunyingcharoen; Johannes Z. Groenewald

To ensure a stable platform for fungal taxonomy, it is of paramount importance that the genetic application of generic names be based on their DNA sequence data, and wherever possible, not morphology or ecology alone. To facilitate this process, a new database, accessible at www.GeneraofFungi.org (GoF) was established, which will allow deposition of metadata linked to holo-, lecto-, neo- or epitype specimens, cultures and DNA sequence data of the type species of genera. Although there are presently more than 18 000 fungal genera described, we aim to initially focus on the subset of names that have been placed on the “Without-prejudice List of Protected Generic Names of Fungi” (see IMA Fungus 4(2): 381–443, 2013). To enable the global mycological community to keep track of typification events and avoid duplication, special MycoBank Typification identfiers (MBT) will be issued upon deposit of metadata in MycoBank. MycoBank is linked to GoF, thus deposited metadata of generic type species will be displayed in GoF (and vice versa), but will also be linked to Index Fungorum (IF) and the curated RefSeq Targeted Loci (RTL) database in GenBank at the National Center for Biotechnology Information (NCBI). This initial paper focuses on eight genera of appendaged coelomycetes, the type species of which are neo- or epitypified here: Bartalinia (Bartalinia robillardoides; Amphisphaeriaceae, Xylariales), Chaetospermum (Chaetospermum chaetosporum, incertae sedis, Sebacinales), Coniella (Coniella fragariae, Schizoparmaceae, Diaporthales), Crinitospora (Crinitospora pulchra, Melanconidaceae, Diaporthales), Eleutheromyces (Eleutheromyces subulatus, Helotiales), Kellermania (Kellermania yuccigena, Planistromataceae, Botryosphaeriales), Mastigosporium (Mastigosporium album, Helotiales), and Mycotribulus (Mycotribulus mirabilis, Agaricales). Authors interested in contributing accounts of individual genera to larger multi-authored papers to be published in IMA Fungus, should contact the associate editors listed below for the major groups of fungi on the List of Protected Generic Names for Fungi.

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Conrad L. Schoch

National Institutes of Health

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Jon K. Magnuson

Pacific Northwest National Laboratory

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Scott E. Baker

Pacific Northwest National Laboratory

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G. Holz

Stellenbosch University

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Johannes Z. Groenewald

Centraalbureau voor Schimmelcultures

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Asaf Salamov

United States Department of Energy

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Astrid Terry

United States Department of Energy

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