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Dive into the research topics where Florian Maumus is active.

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Featured researches published by Florian Maumus.


Nature | 2008

The Phaeodactylum genome reveals the evolutionary history of diatom genomes.

Chris Bowler; Andrew E. Allen; Jonathan H. Badger; Jane Grimwood; Kamel Jabbari; Alan Kuo; Uma Maheswari; Cindy Martens; Florian Maumus; Robert Otillar; Edda Rayko; Asaf Salamov; Klaas Vandepoele; Bank Beszteri; Ansgar Gruber; Marc Heijde; Michael Katinka; Thomas Mock; Klaus Valentin; Frederic Verret; John A. Berges; Colin Brownlee; Jean-Paul Cadoret; Chang Jae Choi; Sacha Coesel; Alessandra De Martino; J. Chris Detter; Colleen Durkin; Angela Falciatore; Jérome Fournet

Diatoms are photosynthetic secondary endosymbionts found throughout marine and freshwater environments, and are believed to be responsible for around one-fifth of the primary productivity on Earth. The genome sequence of the marine centric diatom Thalassiosira pseudonana was recently reported, revealing a wealth of information about diatom biology. Here we report the complete genome sequence of the pennate diatom Phaeodactylum tricornutum and compare it with that of T. pseudonana to clarify evolutionary origins, functional significance and ubiquity of these features throughout diatoms. In spite of the fact that the pennate and centric lineages have only been diverging for 90 million years, their genome structures are dramatically different and a substantial fraction of genes (∼40%) are not shared by these representatives of the two lineages. Analysis of molecular divergence compared with yeasts and metazoans reveals rapid rates of gene diversification in diatoms. Contributing factors include selective gene family expansions, differential losses and gains of genes and introns, and differential mobilization of transposable elements. Most significantly, we document the presence of hundreds of genes from bacteria. More than 300 of these gene transfers are found in both diatoms, attesting to their ancient origins, and many are likely to provide novel possibilities for metabolite management and for perception of environmental signals. These findings go a long way towards explaining the incredible diversity and success of the diatoms in contemporary oceans.


Nature | 2010

The Ectocarpus genome and the independent evolution of multicellularity in brown algae

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.


Nature | 2013

Pan genome of the phytoplankton Emiliania underpins its global distribution

Betsy A. Read; Jessica Kegel; Mary J. Klute; Alan Kuo; Stephane C. Lefebvre; Florian Maumus; Christoph Mayer; John P. Miller; Adam Monier; Asaf Salamov; Jeremy R. Young; Maria Aguilar; Jean-Michel Claverie; Stephan Frickenhaus; Karina Gonzalez; Emily K. Herman; Yao-Cheng Lin; Johnathan A. Napier; Hiroyuki Ogata; Analissa F Sarno; Jeremy Shmutz; Declan C. Schroeder; Frederic Verret; Peter von Dassow; Klaus Valentin; Yves Van de Peer; Glen L. Wheeler; Emiliana Huxleyi; Joel B. Dacks; Charles F. Delwiche

Coccolithophores have influenced the global climate for over 200 million years. These marine phytoplankton can account for 20 per cent of total carbon fixation in some systems. They form blooms that can occupy hundreds of thousands of square kilometres and are distinguished by their elegantly sculpted calcium carbonate exoskeletons (coccoliths), rendering them visible from space. Although coccolithophores export carbon in the form of organic matter and calcite to the sea floor, they also release CO2 in the calcification process. Hence, they have a complex influence on the carbon cycle, driving either CO2 production or uptake, sequestration and export to the deep ocean. Here we report the first haptophyte reference genome, from the coccolithophore Emiliania huxleyi strain CCMP1516, and sequences from 13 additional isolates. Our analyses reveal a pan genome (core genes plus genes distributed variably between strains) probably supported by an atypical complement of repetitive sequence in the genome. Comparisons across strains demonstrate that E. huxleyi, which has long been considered a single species, harbours extensive genome variability reflected in different metabolic repertoires. Genome variability within this species complex seems to underpin its capacity both to thrive in habitats ranging from the equator to the subarctic and to form large-scale episodic blooms under a wide variety of environmental conditions.


Scientific Reports | 2017

Two genomes of highly polyphagous lepidopteran pests (Spodoptera frugiperda, Noctuidae) with different host-plant ranges

Anaïs Gouin; Anthony Bretaudeau; Kiwoong Nam; Sylvie Gimenez; Jean-Marc Aury; Bernard Duvic; Frédérique Hilliou; Nicolas Durand; Nicolas Montagné; Isabelle Darboux; Suyog S. Kuwar; Thomas Chertemps; David Siaussat; Anne Bretschneider; Yves Moné; Seung-Joon Ahn; Sabine Hänniger; Anne-Sophie Gosselin Grenet; David Neunemann; Florian Maumus; Isabelle Luyten; Karine Labadie; Wei Xu; Fotini Koutroumpa; Jean-Michel Escoubas; Angel Llopis; Martine Maïbèche-Coisne; Fanny Salasc; Archana Tomar; Alisha Anderson

Emergence of polyphagous herbivorous insects entails significant adaptation to recognize, detoxify and digest a variety of host-plants. Despite of its biological and practical importance - since insects eat 20% of crops - no exhaustive analysis of gene repertoires required for adaptations in generalist insect herbivores has previously been performed. The noctuid moth Spodoptera frugiperda ranks as one of the world’s worst agricultural pests. This insect is polyphagous while the majority of other lepidopteran herbivores are specialist. It consists of two morphologically indistinguishable strains (“C” and “R”) that have different host plant ranges. To describe the evolutionary mechanisms that both enable the emergence of polyphagous herbivory and lead to the shift in the host preference, we analyzed whole genome sequences from laboratory and natural populations of both strains. We observed huge expansions of genes associated with chemosensation and detoxification compared with specialist Lepidoptera. These expansions are largely due to tandem duplication, a possible adaptation mechanism enabling polyphagy. Individuals from natural C and R populations show significant genomic differentiation. We found signatures of positive selection in genes involved in chemoreception, detoxification and digestion, and copy number variation in the two latter gene families, suggesting an adaptive role for structural variation.


Nucleic Acids Research | 2009

Gene silencing in the marine diatom Phaeodactylum tricornutum

Valentina De Riso; Raffaella Raniello; Florian Maumus; Alessandra Rogato; Chris Bowler; Angela Falciatore

Diatoms are a major but poorly understood phytoplankton group. The recent completion of two whole genome sequences has revealed that they contain unique combinations of genes, likely recruited during their history as secondary endosymbionts, as well as by horizontal gene transfer from bacteria. A major limitation for the study of diatom biology and gene function is the lack of tools to generate targeted gene knockout or knockdown mutants. In this work, we have assessed the possibility of triggering gene silencing in Phaeodactylum tricornutum using constructs containing either anti-sense or inverted repeat sequences of selected target genes. We report the successful silencing of a GUS reporter gene expressed in transgenic lines, as well as the knockdown of endogenous phytochrome (DPH1) and cryptochrome (CPF1) genes. To highlight the utility of the approach we also report the first phenotypic characterization of a diatom mutant (cpf1). Our data open the way for reverse genetics in diatoms and represent a major advance for understanding their biology and ecology. Initial molecular analyses reveal that targeted downregulation likely occurs through transcriptional and post-transcriptional gene silencing mechanisms. Interestingly, molecular players involved in RNA silencing in other eukaryotes are only poorly conserved in diatoms.


Nature Genetics | 2013

The Capsella rubella genome and the genomic consequences of rapid mating system evolution

Tanja Slotte; Khaled M. Hazzouri; J. Arvid Ågren; Daniel Koenig; Florian Maumus; Ya-Long Guo; Kim A. Steige; Adrian E. Platts; Juan S. Escobar; L. Killian Newman; Wei Wang; Terezie Mandáková; Emilio Vello; Lisa M. Smith; Stefan R. Henz; Joshua G. Steffen; Shohei Takuno; Yaniv Brandvain; Graham Coop; Peter Andolfatto; Tina T. Hu; Mathieu Blanchette; Richard M. Clark; Hadi Quesneville; Magnus Nordborg; Brandon S. Gaut; Martin A. Lysak; Jerry Jenkins; Jane Grimwood; Jarrod Chapman

The shift from outcrossing to selfing is common in flowering plants, but the genomic consequences and the speed at which they emerge remain poorly understood. An excellent model for understanding the evolution of self fertilization is provided by Capsella rubella, which became self compatible <200,000 years ago. We report a C. rubella reference genome sequence and compare RNA expression and polymorphism patterns between C. rubella and its outcrossing progenitor Capsella grandiflora. We found a clear shift in the expression of genes associated with flowering phenotypes, similar to that seen in Arabidopsis, in which self fertilization evolved about 1 million years ago. Comparisons of the two Capsella species showed evidence of rapid genome-wide relaxation of purifying selection in C. rubella without a concomitant change in transposable element abundance. Overall we document that the transition to selfing may be typified by parallel shifts in gene expression, along with a measurable reduction of purifying selection.


Nucleic Acids Research | 2011

The Gypsy Database (GyDB) of mobile genetic elements: release 2.0

Carlos Llorens; Ricardo Futami; Laura Covelli; Laura Domínguez-Escribá; Jose M. Viu; Daniel Tamarit; José Aguilar-Rodríguez; Miguel Vicente-Ripolles; Gonzalo Fuster; Guillermo P. Bernet; Florian Maumus; Alfonso Muñoz-Pomer; José M. Sempere; Amparo Latorre; Andrés Moya

This article introduces the second release of the Gypsy Database of Mobile Genetic Elements (GyDB 2.0): a research project devoted to the evolutionary dynamics of viruses and transposable elements based on their phylogenetic classification (per lineage and protein domain). The Gypsy Database (GyDB) is a long-term project that is continuously progressing, and that owing to the high molecular diversity of mobile elements requires to be completed in several stages. GyDB 2.0 has been powered with a wiki to allow other researchers participate in the project. The current database stage and scope are long terminal repeats (LTR) retroelements and relatives. GyDB 2.0 is an update based on the analysis of Ty3/Gypsy, Retroviridae, Ty1/Copia and Bel/Pao LTR retroelements and the Caulimoviridae pararetroviruses of plants. Among other features, in terms of the aforementioned topics, this update adds: (i) a variety of descriptions and reviews distributed in multiple web pages; (ii) protein-based phylogenies, where phylogenetic levels are assigned to distinct classified elements; (iii) a collection of multiple alignments, lineage-specific hidden Markov models and consensus sequences, called GyDB collection; (iv) updated RefSeq databases and BLAST and HMM servers to facilitate sequence characterization of new LTR retroelement and caulimovirus queries; and (v) a bibliographic server. GyDB 2.0 is available at http://gydb.org.


Nature Genetics | 2014

The genome of the stress-tolerant wild tomato species Solanum pennellii

Anthony Bolger; Federico Scossa; Marie E. Bolger; Christa Lanz; Florian Maumus; Takayuki Tohge; Hadi Quesneville; Saleh Alseekh; Iben Sørensen; Gabriel Lichtenstein; Eric A. Fich; Mariana Conte; Heike Keller; Korbinian Schneeberger; Rainer Schwacke; Itai Ofner; Julia Vrebalov; Yimin Xu; Sonia Osorio; Saulo Alves Aflitos; Elio Schijlen; José M. Jiménez-Gómez; Malgorzata Ryngajllo; Seisuke Kimura; Ravi Kumar; Daniel Koenig; Lauren R. Headland; Julin N. Maloof; Neelima Sinha; Roeland C. H. J. van Ham

Solanum pennellii is a wild tomato species endemic to Andean regions in South America, where it has evolved to thrive in arid habitats. Because of its extreme stress tolerance and unusual morphology, it is an important donor of germplasm for the cultivated tomato Solanum lycopersicum. Introgression lines (ILs) in which large genomic regions of S. lycopersicum are replaced with the corresponding segments from S. pennellii can show remarkably superior agronomic performance. Here we describe a high-quality genome assembly of the parents of the IL population. By anchoring the S. pennellii genome to the genetic map, we define candidate genes for stress tolerance and provide evidence that transposable elements had a role in the evolution of these traits. Our work paves a path toward further tomato improvement and for deciphering the mechanisms underlying the myriad other agronomic traits that can be improved with S. pennellii germplasm.


Nature | 2016

The genome of the seagrass Zostera marina reveals angiosperm adaptation to the sea

Jeanine L. Olsen; Pierre Rouzé; Bram Verhelst; Yao-Cheng Lin; Till Bayer; Jonas Collén; Emanuela Dattolo; Emanuele De Paoli; Simon M. Dittami; Florian Maumus; Gurvan Michel; Anna R. Kersting; Chiara Lauritano; Rolf Lohaus; Mats Töpel; Thierry Tonon; Kevin Vanneste; Mojgan Amirebrahimi; Janina Brakel; Christoffer Boström; Mansi Chovatia; Jane Grimwood; Jerry Jenkins; Alexander Jueterbock; Amy Mraz; Wytze T. Stam; Hope Tice; Erich Bornberg-Bauer; Pamela J. Green; Gareth A. Pearson

Seagrasses colonized the sea on at least three independent occasions to form the basis of one of the most productive and widespread coastal ecosystems on the planet. Here we report the genome of Zostera marina (L.), the first, to our knowledge, marine angiosperm to be fully sequenced. This reveals unique insights into the genomic losses and gains involved in achieving the structural and physiological adaptations required for its marine lifestyle, arguably the most severe habitat shift ever accomplished by flowering plants. Key angiosperm innovations that were lost include the entire repertoire of stomatal genes, genes involved in the synthesis of terpenoids and ethylene signalling, and genes for ultraviolet protection and phytochromes for far-red sensing. Seagrasses have also regained functions enabling them to adjust to full salinity. Their cell walls contain all of the polysaccharides typical of land plants, but also contain polyanionic, low-methylated pectins and sulfated galactans, a feature shared with the cell walls of all macroalgae and that is important for ion homoeostasis, nutrient uptake and O2/CO2 exchange through leaf epidermal cells. The Z. marina genome resource will markedly advance a wide range of functional ecological studies from adaptation of marine ecosystems under climate warming, to unravelling the mechanisms of osmoregulation under high salinities that may further inform our understanding of the evolution of salt tolerance in crop plants.


Nature plants | 2015

Genome expansion of Arabis alpina linked with retrotransposition and reduced symmetric DNA methylation

Eva Maria Willing; Vimal Rawat; Terezie Mandáková; Florian Maumus; Geo Velikkakam James; Karl Nordström; Claude Becker; Norman Warthmann; Claudia Chica; Bogna Szarzynska; Matthias Zytnicki; Maria C. Albani; Christiane Kiefer; Sara Bergonzi; Loren Castaings; Julieta L. Mateos; Markus C. Berns; Nora Bujdoso; Thomas Piofczyk; Laura de Lorenzo; Cristina Barrero-Sicilia; Isabel Mateos; Mathieu Piednoël; Jörg Hagmann; Romy Chen-Min-Tao; Raquel Iglesias-Fernández; Stephan C. Schuster; Carlos Alonso-Blanco; François Roudier; Pilar Carbonero

Despite evolutionary conserved mechanisms to silence transposable element activity, there are drastic differences in the abundance of transposable elements even among closely related plant species. We conducted a de novo assembly for the 375 Mb genome of the perennial model plant, Arabis alpina. Analysing this genome revealed long-lasting and recent transposable element activity predominately driven by Gypsy long terminal repeat retrotransposons, which extended the low-recombining pericentromeres and transformed large formerly euchromatic regions into repeat-rich pericentromeric regions. This reduced capacity for long terminal repeat retrotransposon silencing and removal in A. alpina co-occurs with unexpectedly low levels of DNA methylation. Most remarkably, the striking reduction of symmetrical CG and CHG methylation suggests weakened DNA methylation maintenance in A. alpina compared with Arabidopsis thaliana. Phylogenetic analyses indicate a highly dynamic evolution of some components of methylation maintenance machinery that might be related to the unique methylation in A. alpina.

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Hadi Quesneville

Institut national de la recherche agronomique

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Chris Bowler

École Normale Supérieure

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Andrew E. Allen

J. Craig Venter Institute

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Thomas Mock

University of East Anglia

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Colin Brownlee

Marine Biological Association of the United Kingdom

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Asaf Salamov

United States Department of Energy

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Bank Beszteri

Alfred Wegener Institute for Polar and Marine Research

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