Stefan A. Rensing
University of Marburg
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Featured researches published by Stefan A. Rensing.
Nature | 2010
J. Mark Cock; Lieven Sterck; Pierre Rouzé; Delphine Scornet; Andrew E. Allen; Grigoris D. Amoutzias; Véronique Anthouard; François Artiguenave; Jean-Marc Aury; Jonathan H. Badger; Bank Beszteri; Kenny Billiau; Eric Bonnet; John H. Bothwell; Chris Bowler; Catherine Boyen; Colin Brownlee; Carl J. Carrano; Bénédicte Charrier; Ga Youn Cho; Susana M. Coelho; Jonas Collén; Erwan Corre; Corinne Da Silva; Ludovic Delage; Nicolas Delaroque; Simon M. Dittami; Sylvie Doulbeau; Marek Eliáš; Garry Farnham
Brown algae (Phaeophyceae) are complex photosynthetic organisms with a very different evolutionary history to green plants, to which they are only distantly related. These seaweeds are the dominant species in rocky coastal ecosystems and they exhibit many interesting adaptations to these, often harsh, environments. Brown algae are also one of only a small number of eukaryotic lineages that have evolved complex multicellularity (Fig. 1). We report the 214 million base pair (Mbp) genome sequence of the filamentous seaweed Ectocarpus siliculosus (Dillwyn) Lyngbye, a model organism for brown algae, closely related to the kelps (Fig. 1). Genome features such as the presence of an extended set of light-harvesting and pigment biosynthesis genes and new metabolic processes such as halide metabolism help explain the ability of this organism to cope with the highly variable tidal environment. The evolution of multicellularity in this lineage is correlated with the presence of a rich array of signal transduction genes. Of particular interest is the presence of a family of receptor kinases, as the independent evolution of related molecules has been linked with the emergence of multicellularity in both the animal and green plant lineages. The Ectocarpus genome sequence represents an important step towards developing this organism as a model species, providing the possibility to combine genomic and genetic approaches to explore these and other aspects of brown algal biology further.
Nucleic Acids Research | 2010
Paulino Pérez-Rodríguez; Diego Mauricio Riaño-Pachón; Luiz Gustavo Guedes Corrêa; Stefan A. Rensing; Birgit Kersten; Bernd Mueller-Roeber
The Plant Transcription Factor Database (PlnTFDB; http://plntfdb.bio.uni-potsdam.de/v3.0/) is an integrative database that provides putatively complete sets of transcription factors (TFs) and other transcriptional regulators (TRs) in plant species (sensu lato) whose genomes have been completely sequenced and annotated. The complete sets of 84 families of TFs and TRs from 19 species ranging from unicellular red and green algae to angiosperms are included in PlnTFDB, representing >1.6 billion years of evolution of gene regulatory networks. For each gene family, a basic description is provided that is complemented by literature references, and multiple sequence alignments of protein domains. TF or TR gene entries include information of expressed sequence tags, 3D protein structures of homologous proteins, domain architecture and cross-links to other computational resources online. Moreover, the different species in PlnTFDB are linked to each other by means of orthologous genes facilitating cross-species comparisons.
Science | 2010
Simon Prochnik; James G. Umen; Aurora M. Nedelcu; Armin Hallmann; Stephen M. Miller; Ichiro Nishii; Patrick J. Ferris; Alan Kuo; Therese Mitros; Lillian K. Fritz-Laylin; Uffe Hellsten; Jarrod Chapman; Oleg Simakov; Stefan A. Rensing; Astrid Terry; Jasmyn Pangilinan; Vladimir V. Kapitonov; Jerzy Jurka; Asaf Salamov; Harris Shapiro; Jeremy Schmutz; Jane Grimwood; Erika Lindquist; Susan Lucas; Igor V. Grigoriev; Rüdiger Schmitt; David L. Kirk; Daniel S. Rokhsar
Going Multicellular The volvocine algae include both the unicellular Chlamydomonas and the multicellular Volvox, which diverged from one another 50 to 200 million years ago. Prochnik et al. (p. 223) compared the Volvox genome with that of Chlamydomonas to identify any genomic innovations that might have been associated with the transition to multicellularity. Size changes were observed in several protein families in Volvox, but, overall, the Volvox genome and predicted proteome were highly similar to those of Chlamydomonas. Thus, biological complexity can arise without major changes in genome content or protein domains. Comparison of the Chlamydomonas and Volvox genomes show few differences, despite their divergent life histories. The multicellular green alga Volvox carteri and its morphologically diverse close relatives (the volvocine algae) are well suited for the investigation of the evolution of multicellularity and development. We sequenced the 138–mega–base pair genome of V. carteri and compared its ~14,500 predicted proteins to those of its unicellular relative Chlamydomonas reinhardtii. Despite fundamental differences in organismal complexity and life history, the two species have similar protein-coding potentials and few species-specific protein-coding gene predictions. Volvox is enriched in volvocine-algal–specific proteins, including those associated with an expanded and highly compartmentalized extracellular matrix. Our analysis shows that increases in organismal complexity can be associated with modifications of lineage-specific proteins rather than large-scale invention of protein-coding capacity.
Proceedings of the National Academy of Sciences of the United States of America | 2013
Emilie Tisserant; Mathilde Malbreil; Alan Kuo; Annegret Kohler; Aikaterini Symeonidi; Raffaella Balestrini; Philippe Charron; Nina Duensing; Nicolas Frei dit Frey; Vivienne Gianinazzi-Pearson; Luz B. Gilbert; Yoshihiro Handa; Joshua R. Herr; Mohamed Hijri; Raman Koul; Masayoshi Kawaguchi; Franziska Krajinski; Peter J. Lammers; Frédéric Masclaux; Claude Murat; Emmanuelle Morin; Steve Ndikumana; Marco Pagni; Denis Petitpierre; Natalia Requena; Pawel Rosikiewicz; Rohan Riley; Katsuharu Saito; Hélène San Clemente; Harris Shapiro
Significance The arbuscular mycorrhizal symbiosis between fungi of the Glomeromycota phylum and plants involves more than two-thirds of all known plant species, including important crop species. This mutualistic symbiosis, involving one of the oldest fungal lineages, is arguably the most ecologically and agriculturally important symbiosis in terrestrial ecosystems. The Glomeromycota are unique in that their spores and coenocytic hyphae contain hundreds of nuclei in a common cytoplasm, which raises important questions about the natural selection, population genetics, and gene expression of these highly unusual organisms. Study of the genome of Rhizophagus irregularis provides insight into genes involved in obligate biotrophy and mycorrhizal symbioses and the evolution of an ancient asexual organism, and thus is of fundamental importance to the field of genome evolution. The mutualistic symbiosis involving Glomeromycota, a distinctive phylum of early diverging Fungi, is widely hypothesized to have promoted the evolution of land plants during the middle Paleozoic. These arbuscular mycorrhizal fungi (AMF) perform vital functions in the phosphorus cycle that are fundamental to sustainable crop plant productivity. The unusual biological features of AMF have long fascinated evolutionary biologists. The coenocytic hyphae host a community of hundreds of nuclei and reproduce clonally through large multinucleated spores. It has been suggested that the AMF maintain a stable assemblage of several different genomes during the life cycle, but this genomic organization has been questioned. Here we introduce the 153-Mb haploid genome of Rhizophagus irregularis and its repertoire of 28,232 genes. The observed low level of genome polymorphism (0.43 SNP per kb) is not consistent with the occurrence of multiple, highly diverged genomes. The expansion of mating-related genes suggests the existence of cryptic sex-related processes. A comparison of gene categories confirms that R. irregularis is close to the Mucoromycotina. The AMF obligate biotrophy is not explained by genome erosion or any related loss of metabolic complexity in central metabolism, but is marked by a lack of genes encoding plant cell wall-degrading enzymes and of genes involved in toxin and thiamine synthesis. A battery of mycorrhiza-induced secreted proteins is expressed in symbiotic tissues. The present comprehensive repertoire of R. irregularis genes provides a basis for future research on symbiosis-related mechanisms in Glomeromycota.
Science | 2012
Dana C. Price; Cheong Xin Chan; Hwan Su Yoon; Eun Chan Yang; Huan Qiu; Andreas P. M. Weber; Rainer Schwacke; Jeferson Gross; Nicolas A. Blouin; Chris E. Lane; Adrian Reyes-Prieto; Dion G. Durnford; Jonathan A.D. Neilson; B. Franz Lang; Gertraud Burger; Jürgen M. Steiner; Wolfgang Löffelhardt; Jonathan E. Meuser; Matthew C. Posewitz; Steven G. Ball; Maria Cecilia Arias; Bernard Henrissat; Pedro M. Coutinho; Stefan A. Rensing; Aikaterini Symeonidi; Harshavardhan Doddapaneni; Beverley R. Green; Veeran D. Rajah; Jeffrey L. Boore; Debashish Bhattacharya
Plastid Origins The glaucophytes, represented by the alga Cyanophora paradoxa, are the putative sister group of red and green algae and plants, which together comprise the founding group of photosynthetic eukaryotes, the Plantae. In their analysis of the genome of C. paradoxa, Price et al. (p. 843; see the Perspective by Spiegel) demonstrate a unique origin for the plastid in the ancestor of this supergroup, which retains much of the ancestral diversity in genes involved in carbohydrate metabolism and fermentation, as well as in the gene content of the mitochondrial genome. Moreover, about 3.3% of nuclear genes in C. paradoxa seem to carry a signal of cyanobacterial ancestry, and key genes involved in starch biosynthesis are derived from energy parasites such as Chlamydiae. Rapid radiation, reticulate evolution via horizontal gene transfer, high rates of gene divergence, loss, and replacement, may have diffused the evolutionary signals within this supergroup, which perhaps explains previous difficulties in resolving its evolutionary history. An ancient algal genome suggests a unique origin of the plastid in the ancestor to plants, algae, and glaucophytes. The primary endosymbiotic origin of the plastid in eukaryotes more than 1 billion years ago led to the evolution of algae and plants. We analyzed draft genome and transcriptome data from the basally diverging alga Cyanophora paradoxa and provide evidence for a single origin of the primary plastid in the eukaryote supergroup Plantae. C. paradoxa retains ancestral features of starch biosynthesis, fermentation, and plastid protein translocation common to plants and algae but lacks typical eukaryotic light-harvesting complex proteins. Traces of an ancient link to parasites such as Chlamydiae were found in the genomes of C. paradoxa and other Plantae. Apparently, Chlamydia-like bacteria donated genes that allow export of photosynthate from the plastid and its polymerization into storage polysaccharide in the cytosol.
Nature | 2012
Bruce A. Curtis; Goro Tanifuji; Fabien Burki; Ansgar Gruber; Manuel Irimia; Shinichiro Maruyama; Maria Cecilia Arias; Steven G. Ball; Gillian H. Gile; Yoshihisa Hirakawa; Julia F. Hopkins; Alan Kuo; Stefan A. Rensing; Jeremy Schmutz; Aikaterini Symeonidi; Marek Eliáš; Robert J M Eveleigh; Emily K. Herman; Mary J. Klute; Takuro Nakayama; Miroslav Oborník; Adrian Reyes-Prieto; E. Virginia Armbrust; Stephen J. Aves; Robert G. Beiko; Pedro M. Coutinho; Joel B. Dacks; Dion G. Durnford; Naomi M. Fast; Beverley R. Green
Cryptophyte and chlorarachniophyte algae are transitional forms in the widespread secondary endosymbiotic acquisition of photosynthesis by engulfment of eukaryotic algae. Unlike most secondary plastid-bearing algae, miniaturized versions of the endosymbiont nuclei (nucleomorphs) persist in cryptophytes and chlorarachniophytes. To determine why, and to address other fundamental questions about eukaryote–eukaryote endosymbiosis, we sequenced the nuclear genomes of the cryptophyte Guillardia theta and the chlorarachniophyte Bigelowiella natans. Both genomes have >21,000 protein genes and are intron rich, and B. natans exhibits unprecedented alternative splicing for a single-celled organism. Phylogenomic analyses and subcellular targeting predictions reveal extensive genetic and biochemical mosaicism, with both host- and endosymbiont-derived genes servicing the mitochondrion, the host cell cytosol, the plastid and the remnant endosymbiont cytosol of both algae. Mitochondrion-to-nucleus gene transfer still occurs in both organisms but plastid-to-nucleus and nucleomorph-to-nucleus transfers do not, which explains why a small residue of essential genes remains locked in each nucleomorph.
New Phytologist | 2012
Emilie Tisserant; Annegret Kohler; P. Dozolme-Seddas; Raffaella Balestrini; Karim Benabdellah; Alexandre Colard; Daniel Croll; C. da Silva; S. K. Gomez; Raman Koul; Nuria Ferrol; Valentina Fiorilli; Damien Formey; Philipp Franken; Nicole Helber; Mohamed Hijri; Luisa Lanfranco; Erika Lindquist; Y. Liu; Mathilde Malbreil; Emmanuelle Morin; Julie Poulain; Harris Shapiro; D. van Tuinen; A. Waschke; Concepción Azcón-Aguilar; Guillaume Bécard; Paola Bonfante; Maria J. Harrison; Helge Küster
• The arbuscular mycorrhizal symbiosis is arguably the most ecologically important eukaryotic symbiosis, yet it is poorly understood at the molecular level. To provide novel insights into the molecular basis of symbiosis-associated traits, we report the first genome-wide analysis of the transcriptome from Glomus intraradices DAOM 197198. • We generated a set of 25,906 nonredundant virtual transcripts (NRVTs) transcribed in germinated spores, extraradical mycelium and symbiotic roots using Sanger and 454 sequencing. NRVTs were used to construct an oligoarray for investigating gene expression. • We identified transcripts coding for the meiotic recombination machinery, as well as meiosis-specific proteins, suggesting that the lack of a known sexual cycle in G. intraradices is not a result of major deletions of genes essential for sexual reproduction and meiosis. Induced expression of genes encoding membrane transporters and small secreted proteins in intraradical mycelium, together with the lack of expression of hydrolytic enzymes acting on plant cell wall polysaccharides, are all features of G. intraradices that are shared with ectomycorrhizal symbionts and obligate biotrophic pathogens. • Our results illuminate the genetic basis of symbiosis-related traits of the most ancient lineage of plant biotrophs, advancing future research on these agriculturally and ecologically important symbionts.
Science | 2013
Gerald Schönknecht; Wei-Hua Chen; Chad M. Ternes; Guillaume G. Barbier; Roshan P. Shrestha; Mario Stanke; Andrea Bräutigam; Brett J. Baker; Jillian F. Banfield; R. Michael Garavito; Kevin M. Carr; Curtis G. Wilkerson; Stefan A. Rensing; David Gagneul; Nicholas E. Dickenson; Christine Oesterhelt; Martin J. Lercher; Andreas P. M. Weber
Hot, Toxic Eukaryote Unusually, the single-celled eukaryote red alga, Galdieria sulphuraria, can thrive in hot, acidic springs. This organism is endowed with extraordinary metabolic talents and can consume a variety of strange carbohydrates, as well as turn on photosynthesis when the food runs out. Schönknecht et al. (p. 1207; see the Perspective by Rocha) discerned from phylogenetic analysis of its genome that during its evolution, G. sulphuraria appears to have commandeered at least 75 bacterial and archaeal genes by horizontal gene transfer and then applied gene expansion to boost its metabolic repertoire. A mosaic of genes acquired from various phyla enable a red alga to grow abundantly in hot, acidic, and toxic niches. [Also see Perspective by Rocha] Some microbial eukaryotes, such as the extremophilic red alga Galdieria sulphuraria, live in hot, toxic metal-rich, acidic environments. To elucidate the underlying molecular mechanisms of adaptation, we sequenced the 13.7-megabase genome of G. sulphuraria. This alga shows an enormous metabolic flexibility, growing either photoautotrophically or heterotrophically on more than 50 carbon sources. Environmental adaptation seems to have been facilitated by horizontal gene transfer from various bacteria and archaea, often followed by gene family expansion. At least 5% of protein-coding genes of G. sulphuraria were probably acquired horizontally. These proteins are involved in ecologically important processes ranging from heavy-metal detoxification to glycerol uptake and metabolism. Thus, our findings show that a pan-domain gene pool has facilitated environmental adaptation in this unicellular eukaryote.
Journal of Molecular Evolution | 1994
S. Tropf; Thomas Lanz; Stefan A. Rensing; Joachim Schröder; Gudrun Schröder
Chalcone (CHS) and stilbene (STS) synthases are related plant-specific polyketide synthases that are key enzymes in the biosynthesis of flavonoids and of stilbene phytoalexins, respectively. A phylogenetic tree constructed from 34 CHS and four STS sequences revealed that the STS formed no separate cluster but grouped with CHS from the same or related plants. This suggested that STS evolved from CHS several times independently. We attempted to simulate this by site-directed mutagenesis of an interfamily CHS/STS hybrid, which contained 107 amino acids of a CHS from Sinapis alba (N-terminal) and 287 amino acids of a STS from Arachis hypogaea. The hybrid had no enzyme activity. Three amino acid exchanges in the CHS part (Gln-100 to Glu, Val-103 to Met, Val-105 to Arg) were sufficient to obtain low STS activity, and one additional exchange (Gly-23 to Thr) resulted in 20–25% of the parent STS activity. A kinetic analysis indicated (1) that the hybrids had the same Km for the substrate 4-coumaroyl-CoA but a lower Vmax than the parent STS, and (2) that they had a different substrate preference than the parent STS and CHS. Most of the other mutations and their combinations led to enzymatically inactive protein aggregates, suggesting that the subunit folding and/or the dimerization was disturbed. We propose that STS evolved from CHS by a limited number of amino acid exchanges, and that the advantage gained by this enzyme function favored the selection of plants with improved STS activity.
Proceedings of the National Academy of Sciences of the United States of America | 2013
Jonas Collén; Betina M. Porcel; Wilfrid Carré; Steven G. Ball; Cristian Chaparro; Thierry Tonon; Tristan Barbeyron; Gurvan Michel; Benjamin Noel; Klaus Valentin; Marek Eliáš; François Artiguenave; Alok Arun; Jean-Marc Aury; Jose Fernandes Barbosa-Neto; John H. Bothwell; François-Yves Bouget; Loraine Brillet; Francisco Cabello-Hurtado; Salvador Capella-Gutiérrez; Bénédicte Charrier; Lionel Cladière; J. Mark Cock; Susana M. Coelho; Christophe Colleoni; Mirjam Czjzek; Corinne Da Silva; Ludovic Delage; Philippe Deschamps; Simon M. Dittami
Red seaweeds are key components of coastal ecosystems and are economically important as food and as a source of gelling agents, but their genes and genomes have received little attention. Here we report the sequencing of the 105-Mbp genome of the florideophyte Chondrus crispus (Irish moss) and the annotation of the 9,606 genes. The genome features an unusual structure characterized by gene-dense regions surrounded by repeat-rich regions dominated by transposable elements. Despite its fairly large size, this genome shows features typical of compact genomes, e.g., on average only 0.3 introns per gene, short introns, low median distance between genes, small gene families, and no indication of large-scale genome duplication. The genome also gives insights into the metabolism of marine red algae and adaptations to the marine environment, including genes related to halogen metabolism, oxylipins, and multicellularity (microRNA processing and transcription factors). Particularly interesting are features related to carbohydrate metabolism, which include a minimalistic gene set for starch biosynthesis, the presence of cellulose synthases acquired before the primary endosymbiosis showing the polyphyly of cellulose synthesis in Archaeplastida, and cellulases absent in terrestrial plants as well as the occurrence of a mannosylglycerate synthase potentially originating from a marine bacterium. To explain the observations on genome structure and gene content, we propose an evolutionary scenario involving an ancestral red alga that was driven by early ecological forces to lose genes, introns, and intergenetic DNA; this loss was followed by an expansion of genome size as a consequence of activity of transposable elements.